Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8601 |
| ensemblid | ENSG00000147509.14 |
| hgncid | 14600 |
| symbol | RGS20 |
| name | regulator of G protein signaling 20 |
| refseq_nuc | NM_170587.4 |
| refseq_prot | NP_733466.1 |
| ensembl_nuc | ENST00000297313.8 |
| ensembl_prot | ENSP00000297313.3 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 53851795 |
| end | 53959303 |
| strand | + |
| ver | v1.2 |
| region | chr8:53851795-53959303 |
| region5000 | chr8:53846795-53964303 |
| regionname0 | RGS20_chr8_53851795_53959303 |
| regionname5000 | RGS20_chr8_53846795_53964303 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1164 | 242 | 61 | 51 | 100 | 4 | 24 | RGS20_chr8_53846795_53964303 | RGS20 | ATGCC others(1159): Show |
chr8 | 53846795 | 53964303 | ||
| a0001c0002 | 0/0 | 1164 | 8 | 8 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | ATGCC others(1159): Show |
chr8 | 53846795 | 53964303 | ||
| a0001c0003 | 0/0 | 1164 | 6 | 6 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | ATGCC others(1159): Show |
chr8 | 53846795 | 53964303 | ||
| a0001c0004 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | ATGCC others(1159): Show |
chr8 | 53846795 | 53964303 | ||
| a0001c0005 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | ATGCC others(1159): Show |
chr8 | 53846795 | 53964303 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2117 | 115 | 10 | 14 | 80 | 1 | 9 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0001t0002 | 1/0 | 2117 | 94 | 28 | 30 | 18 | 3 | 14 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0001t0003 | 0/0 | 2117 | 16 | 14 | 2 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0001t0004 | 0/0 | 2117 | 4 | 3 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0001t0005 | 0/0 | 2117 | 3 | 2 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0001t0006 | 0/0 | 2113 | 2 | 1 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2108): Show |
chr8 | 53846795 | 53964303 |
| a0001c0001t0007 | 0/0 | 2117 | 2 | 0 | 2 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0001t0008 | 0/0 | 2113 | 2 | 2 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2108): Show |
chr8 | 53846795 | 53964303 |
| a0001c0001t0009 | 0/0 | 2117 | 2 | 0 | 0 | 1 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0001t0010 | 0/0 | 2117 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0001t0011 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0002t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0002t0002 | 0/0 | 2117 | 6 | 6 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0002t0003 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0003t0001 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0003t0002 | 0/0 | 2117 | 3 | 3 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0003t0003 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0003t0004 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0004t0002 | 0/0 | 2117 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| a0001c0005t0002 | 0/0 | 2117 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | AGAGC others(2112): Show |
chr8 | 53846795 | 53964303 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0127 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0007g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0009g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0010g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0002t0003g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0003t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0003t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0004t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| a0001c0005t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0220 | EUR | GBR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0150 | EUR | GBR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0161 | EUR | FIN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | FIN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0043 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0033 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0045 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PUR | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0221 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CDX | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02280 | hp2 | a0001 | c0003 | t0004 | g0027 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0039 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0026 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0029 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0028 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0025 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03209 | hp1 | a0001 | c0005 | t0002 | g0113 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | ESN | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0119 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | BEB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04184 | hp2 | a0001 | c0001 | t0009 | g0128 | SAS | BEB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | STU | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0114 | AFR | YRI | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | YRI | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18975 | hp2 | a0001 | c0001 | t0010 | g0189 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18993 | hp2 | a0001 | c0001 | t0009 | g0136 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0003 | AFR | LWK | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | LWK | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | LWK | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | LWK | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ASW | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ASW | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | GIH | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | GIH | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01123 | hp1 | a0001 | c0004 | t0002 | g0153 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02109 | hp1 | a0001 | c0001 | t0011 | g0208 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02109 | hp2 | a0001 | c0003 | t0002 | g0253 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0246 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0244 | AFR | ACB | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | MSL | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | USA | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | USA | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | USA | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | USA | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0166 | REF | REF | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0127 | REF | REF | RGS20_chr8_53846795_53964303 | RGS20 | chr8 | 53846795 | 53964303 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:53879428 | G | A | 1 | a0001c0003 | 6 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(3): Show |
synonymous_variant | LOW | c.336G>A | p.Pro112Pro | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/6 | 441/2117 | 336/1167 | 112/388 | chr8 | 53879428 | |||
| chr8:53879485 | C | A | 1 | a0001c0002 | 8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
synonymous_variant | LOW | c.393C>A | p.Leu131Leu | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/6 | 498/2117 | 393/1167 | 131/388 | chr8 | 53879485 | |||
| chr8:53954097 | A | G | 1 | a0001c0005 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.765A>G | p.Glu255Glu | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/6 | 870/2117 | 765/1167 | 255/388 | chr8 | 53954097 | |||
| chr8:53958275 | C | T | 1 | a0001c0004 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.984C>T | p.Ser328Ser | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 1089/2117 | 984/1167 | 328/388 | chr8 | 53958275 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:53851831 | G | A | 2 | a0001c0001t0006 a0001c0001t0007 |
4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-69G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/6 | 69 | chr8 | 53851831 | ||||||
| chr8:53958503 | C | T | 1 | a0001c0001t0005 | 3 | HG01978.hp2 HG02055.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*45C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 45 | chr8 | 53958503 | ||||||
| chr8:53958515 | C | T | 1 | a0001c0001t0009 | 2 | HG04184.hp2 NA18993.hp2 |
3_prime_UTR_variant | MODIFIER | c.*57C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 57 | chr8 | 53958515 | ||||||
| chr8:53958634 | T | C | 1 | a0001c0001t0010 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*176T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 176 | chr8 | 53958634 | ||||||
| chr8:53958866 | C | T | 2 | a0001c0001t0004 a0001c0003t0004 |
5 | HG01167.hp1 HG02280.hp2 HG03540.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*408C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 408 | chr8 | 53958866 | ||||||
| chr8:53958992 | AGTAT | A | 2 | a0001c0001t0006 a0001c0001t0008 |
4 | HG01069.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*552_*555delTATG | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 552 | INFO_REALIGN_3_PRIME | chr8 | 53958992 | |||||
| chr8:53959019 | A | G | 1 | a0001c0001t0011 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*561A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 561 | chr8 | 53959019 | ||||||
| chr8:53959028 | C | T | 3 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 |
18 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*570C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 570 | chr8 | 53959028 | ||||||
| chr8:53959197 | A | G | 4 | a0001c0001t0001 a0001c0001t0010 a0001c0002t0001 others(1): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*739A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 6/6 | 739 | chr8 | 53959197 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:53852096 | C | T | 2 | a0001c0001t0002g0257 a0001c0001t0002g0258 |
2 | HG00642.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.165+32C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53852096 | |||||||
| chr8:53852444 | G | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(13): Show |
16 | HG02055.hp2 HG02559.hp1 HG02895.hp2 others(13): Show |
intron_variant | MODIFIER | c.165+380G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53852444 | |||||||
| chr8:53852776 | T | C | 16 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(13): Show |
16 | HG02055.hp2 HG02559.hp1 HG02895.hp2 others(13): Show |
intron_variant | MODIFIER | c.165+712T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53852776 | |||||||
| chr8:53852829 | C | T | 3 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 |
3 | HG02818.hp2 NA19012.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.165+765C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53852829 | |||||||
| chr8:53852878 | C | G | 2 | a0001c0001t0001g0252 a0001c0003t0002g0253 |
2 | HG02109.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.165+814C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53852878 | |||||||
| chr8:53853496 | T | A | 1 | a0001c0001t0002g0017 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.165+1432T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53853496 | |||||||
| chr8:53853754 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.165+1690T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53853754 | |||||||
| chr8:53853981 | G | A | 1 | a0001c0001t0002g0019 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.165+1917G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53853981 | |||||||
| chr8:53854009 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+1945G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854009 | |||||||
| chr8:53854018 | T | TC | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0002g0251 |
3 | HG00642.hp2 HG01099.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.165+1955dupC | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53854018 | ||||||
| chr8:53854208 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0003g0022 a0001c0001t0003g0024 |
3 | HG02886.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.165+2144G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854208 | |||||||
| chr8:53854287 | G | A | 88 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(85): Show |
88 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.165+2223G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854287 | |||||||
| chr8:53854501 | T | C | 5 | a0001c0003t0001g0028 a0001c0003t0002g0025 a0001c0003t0002g0029 others(2): Show |
5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+2437T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854501 | |||||||
| chr8:53854538 | G | C | 23 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(20): Show |
23 | HG02055.hp2 HG02280.hp2 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.165+2474G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854538 | |||||||
| chr8:53854559 | A | G | 21 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(18): Show |
21 | HG02055.hp2 HG02280.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.165+2495A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854559 | |||||||
| chr8:53854964 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.165+2900G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53854964 | |||||||
| chr8:53855016 | A | G | 2 | a0001c0001t0002g0247 a0001c0001t0002g0248 |
2 | HG01074.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.165+2952A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53855016 | |||||||
| chr8:53855135 | G | C | 28 | a0001c0001t0001g0018 a0001c0001t0001g0088 a0001c0001t0001g0089 others(25): Show |
28 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.165+3071G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53855135 | |||||||
| chr8:53855168 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.165+3104G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53855168 | |||||||
| chr8:53855316 | C | T | 15 | a0001c0001t0002g0232 a0001c0001t0002g0235 a0001c0001t0002g0237 others(12): Show |
15 | HG00741.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+3252C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53855316 | |||||||
| chr8:53856034 | A | C | 3 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 |
3 | NA18990.hp1 NA19060.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.165+3970A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53856034 | |||||||
| chr8:53856160 | G | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.165+4096G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53856160 | |||||||
| chr8:53856216 | AT | A | 55 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(52): Show |
55 | HG00323.hp2 HG00741.hp1 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.165+4169delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53856216 | ||||||
| chr8:53856508 | C | T | 2 | a0001c0001t0002g0227 a0001c0001t0002g0228 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.165+4444C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53856508 | |||||||
| chr8:53856523 | A | C | 1 | a0001c0001t0002g0226 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.165+4459A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53856523 | |||||||
| chr8:53856658 | T | G | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.165+4594T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53856658 | |||||||
| chr8:53857393 | G | T | 1 | a0001c0001t0001g0087 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.165+5329G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53857393 | |||||||
| chr8:53857413 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.165+5349T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53857413 | |||||||
| chr8:53857551 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165+5487G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53857551 | |||||||
| chr8:53857739 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.165+5675G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53857739 | |||||||
| chr8:53857747 | A | G | 89 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
89 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.165+5683A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53857747 | |||||||
| chr8:53857974 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.165+5910A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53857974 | |||||||
| chr8:53858265 | T | C | 1 | a0001c0001t0002g0247 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.165+6201T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858265 | |||||||
| chr8:53858300 | C | T | 7 | a0001c0001t0001g0222 a0001c0001t0002g0218 a0001c0001t0002g0219 others(4): Show |
7 | HG00140.hp1 HG01070.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+6236C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858300 | |||||||
| chr8:53858503 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(10): Show |
13 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+6439C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858503 | |||||||
| chr8:53858532 | C | A | 14 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(11): Show |
14 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+6468C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858532 | |||||||
| chr8:53858674 | C | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+6610C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858674 | |||||||
| chr8:53858718 | T | C | 9 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0240 others(6): Show |
9 | HG00741.hp1 HG01109.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+6654T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858718 | |||||||
| chr8:53858741 | G | A | 5 | a0001c0003t0001g0028 a0001c0003t0002g0025 a0001c0003t0002g0029 others(2): Show |
5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+6677G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858741 | |||||||
| chr8:53858845 | T | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+6781T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858845 | |||||||
| chr8:53858892 | T | TA | 82 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0023 others(79): Show |
82 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.165+6848dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53858892 | ||||||
| chr8:53858892 | T | TAA | 10 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0041 others(7): Show |
10 | HG00423.hp2 HG00438.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.165+6847_165+6848d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53858892 | ||||||
| chr8:53858892 | TA | T | 13 | a0001c0001t0001g0110 a0001c0001t0002g0108 a0001c0001t0002g0215 others(10): Show |
13 | HG00642.hp1 HG01099.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+6848delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53858892 | ||||||
| chr8:53858913 | C | A | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165+6849C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53858913 | |||||||
| chr8:53859019 | A | G | 2 | a0001c0003t0002g0025 a0001c0003t0002g0029 |
2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.165+6955A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859019 | |||||||
| chr8:53859209 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.165+7145C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859209 | |||||||
| chr8:53859217 | A | C | 1 | a0001c0001t0002g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+7153A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859217 | |||||||
| chr8:53859217 | A | G | 77 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(74): Show |
77 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.165+7153A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859217 | |||||||
| chr8:53859326 | T | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+7262T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859326 | |||||||
| chr8:53859422 | A | AT | 12 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+7362dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53859422 | ||||||
| chr8:53859652 | A | C | 1 | a0001c0001t0002g0016 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.165+7588A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859652 | |||||||
| chr8:53859673 | C | G | 1 | a0001c0001t0002g0017 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.165+7609C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859673 | |||||||
| chr8:53859673 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.165+7609C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859673 | |||||||
| chr8:53859815 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0125 |
2 | HG02027.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.165+7751G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859815 | |||||||
| chr8:53859852 | A | T | 1 | a0001c0001t0002g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.165+7788A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859852 | |||||||
| chr8:53859907 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.165+7843A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859907 | |||||||
| chr8:53859916 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.165+7852C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859916 | |||||||
| chr8:53859968 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.165+7904A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859968 | |||||||
| chr8:53859994 | T | C | 1 | a0001c0001t0002g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.165+7930T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53859994 | |||||||
| chr8:53860374 | T | C | 60 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(57): Show |
60 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.165+8310T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860374 | |||||||
| chr8:53860520 | G | A | 2 | a0001c0001t0002g0108 a0001c0001t0003g0109 |
2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.165+8456G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860520 | |||||||
| chr8:53860560 | G | GAAGATGC others(4): Show |
77 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(74): Show |
77 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.165+8501_165+8502i others(13): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53860560 | ||||||
| chr8:53860654 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.165+8590T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860654 | |||||||
| chr8:53860692 | G | A | 8 | a0001c0002t0001g0005 a0001c0002t0002g0002 a0001c0002t0002g0004 others(5): Show |
8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+8628G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860692 | |||||||
| chr8:53860708 | C | G | 255 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(252): Show |
255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.165+8644C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860708 | |||||||
| chr8:53860713 | C | G | 2 | a0001c0001t0007g0033 a0001c0001t0007g0045 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.165+8649C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860713 | |||||||
| chr8:53860844 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0110 |
2 | NA18959.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.165+8780G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860844 | |||||||
| chr8:53860982 | A | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+8918A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53860982 | |||||||
| chr8:53861114 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.165+9050C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861114 | |||||||
| chr8:53861311 | G | A | 1 | a0001c0001t0009g0128 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.165+9247G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861311 | |||||||
| chr8:53861335 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.165+9271C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861335 | |||||||
| chr8:53861350 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.165+9286G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861350 | |||||||
| chr8:53861358 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+9294G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861358 | |||||||
| chr8:53861381 | C | T | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165+9317C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861381 | |||||||
| chr8:53861428 | A | G | 2 | a0001c0001t0002g0117 a0001c0001t0002g0210 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.165+9364A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861428 | |||||||
| chr8:53861873 | A | C | 2 | a0001c0001t0002g0227 a0001c0001t0002g0228 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.165+9809A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861873 | |||||||
| chr8:53861949 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+9885C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53861949 | |||||||
| chr8:53862036 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.165+9972G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862036 | |||||||
| chr8:53862139 | A | C | 4 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0007g0033 others(1): Show |
4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+10075A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862139 | |||||||
| chr8:53862390 | T | G | 1 | a0001c0001t0002g0129 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.165+10326T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862390 | |||||||
| chr8:53862679 | G | C | 8 | a0001c0002t0001g0005 a0001c0002t0002g0002 a0001c0002t0002g0004 others(5): Show |
8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+10615G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862679 | |||||||
| chr8:53862794 | A | G | 9 | a0001c0001t0002g0235 a0001c0001t0002g0237 a0001c0001t0002g0240 others(6): Show |
9 | HG00741.hp1 HG01109.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+10730A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862794 | |||||||
| chr8:53862868 | G | T | 8 | a0001c0002t0001g0005 a0001c0002t0002g0002 a0001c0002t0002g0004 others(5): Show |
8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+10804G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862868 | |||||||
| chr8:53862953 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0003g0024 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.165+10889C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862953 | |||||||
| chr8:53862970 | A | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+10906A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53862970 | |||||||
| chr8:53863032 | A | G | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.165+10968A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863032 | |||||||
| chr8:53863080 | C | G | 2 | a0001c0001t0002g0038 a0001c0001t0008g0039 |
2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.165+11016C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863080 | |||||||
| chr8:53863132 | C | G | 1 | a0001c0001t0001g0015 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.165+11068C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863132 | |||||||
| chr8:53863229 | C | T | 1 | a0001c0001t0002g0209 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.165+11165C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863229 | |||||||
| chr8:53863269 | G | A | 1 | a0001c0001t0003g0234 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.165+11205G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863269 | |||||||
| chr8:53863292 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.165+11228A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863292 | |||||||
| chr8:53863336 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.165+11272C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863336 | |||||||
| chr8:53863500 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.165+11436G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863500 | |||||||
| chr8:53863533 | A | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+11469A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863533 | |||||||
| chr8:53863702 | T | A | 1 | a0001c0001t0002g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.165+11638T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863702 | |||||||
| chr8:53863727 | C | CT | 14 | a0001c0001t0001g0206 a0001c0001t0001g0225 a0001c0001t0002g0038 others(11): Show |
14 | HG00438.hp1 HG01069.hp2 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.165+11682dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53863727 | ||||||
| chr8:53863727 | CT | C | 27 | a0001c0001t0001g0046 a0001c0001t0001g0088 a0001c0001t0001g0089 others(24): Show |
27 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.165+11682delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53863727 | ||||||
| chr8:53863796 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+11732G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863796 | |||||||
| chr8:53863963 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.165+11899G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53863963 | |||||||
| chr8:53864257 | C | T | 1 | a0001c0003t0001g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.165+12193C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53864257 | |||||||
| chr8:53864277 | A | C | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.165+12213A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53864277 | |||||||
| chr8:53864297 | G | A | 2 | a0001c0001t0002g0038 a0001c0001t0008g0039 |
2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.165+12233G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53864297 | |||||||
| chr8:53864303 | G | A | 8 | a0001c0002t0001g0005 a0001c0002t0002g0002 a0001c0002t0002g0004 others(5): Show |
8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+12239G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53864303 | |||||||
| chr8:53864430 | G | GA | 37 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0047 others(34): Show |
37 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.165+12387dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53864430 | ||||||
| chr8:53864430 | GA | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0074 a0001c0001t0001g0075 others(17): Show |
20 | HG01496.hp2 HG02055.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+12387delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53864430 | ||||||
| chr8:53864475 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.165+12411T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53864475 | |||||||
| chr8:53865154 | T | C | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.165+13090T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865154 | |||||||
| chr8:53865184 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0086 |
2 | NA19056.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.165+13120C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865184 | |||||||
| chr8:53865245 | G | A | 1 | a0001c0001t0003g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.165+13181G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865245 | |||||||
| chr8:53865301 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.165+13237A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865301 | |||||||
| chr8:53865364 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.165+13300G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865364 | |||||||
| chr8:53865422 | T | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+13358T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865422 | |||||||
| chr8:53865757 | C | G | 1 | a0001c0001t0002g0144 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.166-13501C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865757 | |||||||
| chr8:53865862 | T | C | 65 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(62): Show |
65 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.166-13396T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865862 | |||||||
| chr8:53865886 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-13372C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53865886 | |||||||
| chr8:53866042 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.166-13216G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866042 | |||||||
| chr8:53866053 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-13205C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866053 | |||||||
| chr8:53866145 | G | A | 8 | a0001c0002t0001g0005 a0001c0002t0002g0002 a0001c0002t0002g0004 others(5): Show |
8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-13113G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866145 | |||||||
| chr8:53866280 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-12978C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866280 | |||||||
| chr8:53866288 | G | A | 15 | a0001c0001t0001g0041 a0001c0001t0001g0052 a0001c0001t0001g0074 others(12): Show |
15 | HG00438.hp2 HG01496.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.166-12970G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866288 | |||||||
| chr8:53866387 | C | CT | 9 | a0001c0001t0001g0121 a0001c0001t0001g0143 a0001c0001t0002g0020 others(6): Show |
9 | HG01099.hp2 HG02027.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-12858dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53866387 | ||||||
| chr8:53866387 | CT | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG02027.hp2 HG02055.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-12858delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53866387 | ||||||
| chr8:53866918 | C | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(11): Show |
14 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.166-12340C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866918 | |||||||
| chr8:53866957 | C | T | 89 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(86): Show |
89 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.166-12301C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866957 | |||||||
| chr8:53866992 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.166-12266G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53866992 | |||||||
| chr8:53867426 | G | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.166-11832G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867426 | |||||||
| chr8:53867428 | C | T | 5 | a0001c0003t0001g0028 a0001c0003t0002g0025 a0001c0003t0002g0029 others(2): Show |
5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-11830C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867428 | |||||||
| chr8:53867518 | G | A | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.166-11740G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867518 | |||||||
| chr8:53867547 | G | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0202 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.166-11711G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867547 | |||||||
| chr8:53867554 | C | G | 24 | a0001c0001t0001g0018 a0001c0001t0001g0088 a0001c0001t0001g0089 others(21): Show |
24 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.166-11704C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867554 | |||||||
| chr8:53867614 | C | T | 77 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(74): Show |
77 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.166-11644C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867614 | |||||||
| chr8:53867649 | C | T | 220 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(217): Show |
220 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.166-11609C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867649 | |||||||
| chr8:53867658 | T | TCTTC | 87 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0052 others(84): Show |
87 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.166-11556_166-1155 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53867658 | ||||||
| chr8:53867658 | T | TCTTCCTT others(1): Show |
22 | a0001c0001t0001g0018 a0001c0001t0001g0093 a0001c0001t0001g0110 others(19): Show |
22 | HG00140.hp2 HG00438.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.166-11560_166-1155 others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53867658 | ||||||
| chr8:53867658 | T | TCTTCCTT others(5): Show |
2 | a0001c0001t0001g0105 a0001c0001t0001g0206 |
2 | HG01261.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.166-11564_166-1155 others(16): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53867658 | ||||||
| chr8:53867658 | TCTTC | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0046 others(31): Show |
34 | HG00423.hp1 HG01167.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.166-11556_166-1155 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53867658 | ||||||
| chr8:53867706 | T | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-11552T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867706 | |||||||
| chr8:53867711 | G | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-11547G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867711 | |||||||
| chr8:53867945 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.166-11313A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53867945 | |||||||
| chr8:53868039 | T | G | 5 | a0001c0003t0001g0028 a0001c0003t0002g0025 a0001c0003t0002g0029 others(2): Show |
5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-11219T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868039 | |||||||
| chr8:53868484 | G | C | 1 | a0001c0001t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.166-10774G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868484 | |||||||
| chr8:53868495 | G | A | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-10763G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868495 | |||||||
| chr8:53868502 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.166-10756G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868502 | |||||||
| chr8:53868653 | A | AAT | 8 | a0001c0001t0001g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
8 | HG02280.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-10590_166-1058 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53868653 | ||||||
| chr8:53868653 | A | AATAT | 3 | a0001c0001t0001g0015 a0001c0001t0002g0016 a0001c0003t0003g0026 |
3 | HG02055.hp2 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.166-10592_166-1058 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53868653 | ||||||
| chr8:53868697 | T | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-10561T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868697 | |||||||
| chr8:53868733 | G | T | 27 | a0001c0001t0001g0018 a0001c0001t0001g0088 a0001c0001t0001g0089 others(24): Show |
27 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.166-10525G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868733 | |||||||
| chr8:53868909 | C | T | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-10349C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53868909 | |||||||
| chr8:53869088 | A | T | 2 | a0001c0001t0002g0038 a0001c0001t0008g0039 |
2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-10170A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869088 | |||||||
| chr8:53869414 | G | A | 61 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(58): Show |
61 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.166-9844G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869414 | |||||||
| chr8:53869530 | G | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0015 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.166-9728G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869530 | |||||||
| chr8:53869568 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.166-9690C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869568 | |||||||
| chr8:53869591 | G | A | 4 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0007g0033 others(1): Show |
4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-9667G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869591 | |||||||
| chr8:53869605 | T | G | 90 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(87): Show |
90 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.166-9653T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869605 | |||||||
| chr8:53869611 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.166-9647G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869611 | |||||||
| chr8:53869632 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.166-9626C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869632 | |||||||
| chr8:53869746 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-9512C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869746 | |||||||
| chr8:53869869 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-9389G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869869 | |||||||
| chr8:53869871 | G | T | 2 | a0001c0001t0002g0174 a0001c0001t0002g0209 |
2 | NA18961.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.166-9387G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869871 | |||||||
| chr8:53869956 | C | A | 6 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0056 others(3): Show |
6 | NA18963.hp2 NA19055.hp2 NA19056.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-9302C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53869956 | |||||||
| chr8:53870022 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.166-9236A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870022 | |||||||
| chr8:53870108 | A | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(14): Show |
17 | HG02055.hp2 HG02109.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.166-9150A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870108 | |||||||
| chr8:53870244 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.166-9014T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870244 | |||||||
| chr8:53870262 | T | TAC | 4 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0007g0033 others(1): Show |
4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-8976_166-8975d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53870262 | ||||||
| chr8:53870452 | C | T | 4 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0007g0033 others(1): Show |
4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-8806C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870452 | |||||||
| chr8:53870573 | A | T | 3 | a0001c0001t0002g0038 a0001c0001t0008g0039 a0001c0003t0002g0253 |
3 | HG02109.hp2 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-8685A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870573 | |||||||
| chr8:53870641 | T | C | 2 | a0001c0001t0002g0038 a0001c0001t0008g0039 |
2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-8617T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870641 | |||||||
| chr8:53870679 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.166-8579C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870679 | |||||||
| chr8:53870895 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.166-8363G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53870895 | |||||||
| chr8:53871035 | C | T | 8 | a0001c0002t0001g0005 a0001c0002t0002g0002 a0001c0002t0002g0004 others(5): Show |
8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-8223C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871035 | |||||||
| chr8:53871112 | C | CA | 67 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0040 others(64): Show |
67 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.166-8117dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871112 | ||||||
| chr8:53871112 | C | CAA | 11 | a0001c0001t0001g0023 a0001c0001t0001g0047 a0001c0001t0001g0125 others(8): Show |
11 | HG00597.hp1 HG01169.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-8118_166-8117d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871112 | ||||||
| chr8:53871112 | CA | C | 24 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(21): Show |
24 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.166-8117delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871112 | ||||||
| chr8:53871112 | CAA | C | 5 | a0001c0002t0001g0005 a0001c0002t0002g0006 a0001c0002t0002g0007 others(2): Show |
5 | HG02922.hp1 HG03041.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-8118_166-8117d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871112 | ||||||
| chr8:53871112 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0213 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.166-8126_166-8117d others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871112 | ||||||
| chr8:53871112 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0002g0038 a0001c0001t0008g0039 a0001c0003t0002g0253 |
3 | HG02109.hp2 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-8127_166-8117d others(13): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871112 | ||||||
| chr8:53871247 | C | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG00423.hp2 HG04184.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.166-8011C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871247 | |||||||
| chr8:53871512 | G | C | 1 | a0001c0001t0001g0256 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.166-7746G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871512 | |||||||
| chr8:53871624 | A | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | NA18957.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.166-7634A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871624 | |||||||
| chr8:53871624 | AAAT | A | 90 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(87): Show |
90 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.166-7618_166-7616d others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53871624 | ||||||
| chr8:53871627 | T | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0185 |
2 | NA18948.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.166-7631T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871627 | |||||||
| chr8:53871630 | T | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-7628T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871630 | |||||||
| chr8:53871631 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.166-7627A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871631 | |||||||
| chr8:53871707 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0003g0024 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.166-7551A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871707 | |||||||
| chr8:53871824 | C | T | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-7434C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871824 | |||||||
| chr8:53871877 | T | G | 252 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(249): Show |
252 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.166-7381T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871877 | |||||||
| chr8:53871936 | C | T | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-7322C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53871936 | |||||||
| chr8:53872222 | T | A | 1 | a0001c0003t0001g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.166-7036T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872222 | |||||||
| chr8:53872394 | C | A | 1 | a0001c0003t0001g0028 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.166-6864C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872394 | |||||||
| chr8:53872650 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.166-6608A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872650 | |||||||
| chr8:53872780 | C | G | 1 | a0001c0001t0001g0123 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.166-6478C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872780 | |||||||
| chr8:53872839 | T | G | 1 | a0001c0001t0002g0139 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.166-6419T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872839 | |||||||
| chr8:53872869 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-6389C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872869 | |||||||
| chr8:53872901 | A | C | 1 | a0001c0001t0002g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.166-6357A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53872901 | |||||||
| chr8:53873130 | C | T | 61 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(58): Show |
61 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.166-6128C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53873130 | |||||||
| chr8:53873369 | A | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-5889A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53873369 | |||||||
| chr8:53873625 | C | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-5633C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53873625 | |||||||
| chr8:53873781 | G | A | 62 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(59): Show |
62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-5477G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53873781 | |||||||
| chr8:53873915 | C | T | 62 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(59): Show |
62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-5343C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53873915 | |||||||
| chr8:53873924 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0002g0073 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.166-5334T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53873924 | |||||||
| chr8:53874061 | G | A | 2 | a0001c0001t0002g0174 a0001c0001t0002g0209 |
2 | NA18961.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.166-5197G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874061 | |||||||
| chr8:53874129 | G | A | 61 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(58): Show |
61 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.166-5129G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874129 | |||||||
| chr8:53874149 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.166-5109C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874149 | |||||||
| chr8:53874154 | A | T | 1 | a0001c0003t0004g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.166-5104A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874154 | |||||||
| chr8:53874173 | C | T | 62 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(59): Show |
62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-5085C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874173 | |||||||
| chr8:53874367 | G | GGT | 25 | a0001c0001t0001g0010 a0001c0001t0001g0143 a0001c0001t0001g0186 others(22): Show |
25 | HG00323.hp1 HG00741.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.166-4857_166-4856d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874367 | ||||||
| chr8:53874367 | G | GGTGT | 8 | a0001c0001t0002g0117 a0001c0001t0002g0132 a0001c0001t0002g0144 others(5): Show |
8 | HG01891.hp2 HG01978.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-4859_166-4856d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874367 | ||||||
| chr8:53874367 | G | GT | 4 | a0001c0001t0001g0107 a0001c0001t0002g0178 a0001c0001t0002g0216 others(1): Show |
4 | HG01099.hp1 HG01168.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-4891_166-4890i others(3): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874367 | |||||||
| chr8:53874367 | GGT | G | 24 | a0001c0001t0001g0115 a0001c0001t0001g0151 a0001c0001t0001g0160 others(21): Show |
24 | HG00408.hp1 HG00408.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.166-4857_166-4856d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874367 | ||||||
| chr8:53874367 | GGTGT | G | 15 | a0001c0001t0001g0014 a0001c0001t0001g0123 a0001c0001t0001g0152 others(12): Show |
15 | HG00438.hp1 HG01069.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.166-4859_166-4856d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874367 | ||||||
| chr8:53874367 | GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.166-4865_166-4856d others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874367 | ||||||
| chr8:53874367 | GGTGTGTG others(5): Show |
G | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-4867_166-4856d others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874367 | ||||||
| chr8:53874369 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.166-4889T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874369 | |||||||
| chr8:53874391 | TGTGTGTG others(5): Show |
T | 3 | a0001c0001t0001g0048 a0001c0001t0003g0030 a0001c0001t0004g0037 |
3 | HG01167.hp1 HG02630.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.166-4865_166-4854d others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874391 | ||||||
| chr8:53874393 | TGTGTGTG others(3): Show |
T | 56 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(53): Show |
56 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.166-4863_166-4854d others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53874393 | ||||||
| chr8:53874399 | T | C | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-4859T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874399 | |||||||
| chr8:53874401 | T | C | 6 | a0001c0001t0001g0160 a0001c0001t0002g0146 a0001c0001t0002g0157 others(3): Show |
6 | HG01358.hp2 HG02109.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-4857T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874401 | |||||||
| chr8:53874407 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02165.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.166-4851C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874407 | |||||||
| chr8:53874411 | T | C | 62 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(59): Show |
62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-4847T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874411 | |||||||
| chr8:53874416 | T | A | 62 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(59): Show |
62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-4842T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874416 | |||||||
| chr8:53874519 | G | C | 5 | a0001c0003t0001g0028 a0001c0003t0002g0025 a0001c0003t0002g0029 others(2): Show |
5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-4739G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874519 | |||||||
| chr8:53874585 | A | G | 62 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(59): Show |
62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-4673A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874585 | |||||||
| chr8:53874763 | T | C | 1 | a0001c0001t0002g0117 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.166-4495T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874763 | |||||||
| chr8:53874820 | T | G | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-4438T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874820 | |||||||
| chr8:53874838 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.166-4420A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874838 | |||||||
| chr8:53874901 | A | C | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-4357A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53874901 | |||||||
| chr8:53875009 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.166-4249C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875009 | |||||||
| chr8:53875014 | A | G | 5 | a0001c0003t0001g0028 a0001c0003t0002g0025 a0001c0003t0002g0029 others(2): Show |
5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-4244A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875014 | |||||||
| chr8:53875025 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.166-4233C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875025 | |||||||
| chr8:53875044 | A | C | 2 | a0001c0001t0002g0038 a0001c0001t0008g0039 |
2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-4214A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875044 | |||||||
| chr8:53875071 | G | C | 5 | a0001c0003t0001g0028 a0001c0003t0002g0025 a0001c0003t0002g0029 others(2): Show |
5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-4187G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875071 | |||||||
| chr8:53875125 | A | G | 1 | a0001c0003t0002g0253 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.166-4133A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875125 | |||||||
| chr8:53875191 | T | G | 62 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(59): Show |
62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.166-4067T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875191 | |||||||
| chr8:53875233 | A | G | 12 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0007g0033 others(9): Show |
12 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-4025A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875233 | |||||||
| chr8:53875429 | C | CA | 44 | a0001c0001t0001g0089 a0001c0001t0001g0095 a0001c0001t0001g0121 others(41): Show |
44 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.166-3808dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53875429 | ||||||
| chr8:53875429 | C | CAAAA | 5 | a0001c0001t0001g0015 a0001c0001t0002g0016 a0001c0001t0002g0021 others(2): Show |
5 | HG02055.hp2 HG02895.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-3811_166-3808d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53875429 | ||||||
| chr8:53875429 | CA | C | 5 | a0001c0001t0001g0116 a0001c0001t0001g0160 a0001c0001t0002g0196 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-3808delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53875429 | ||||||
| chr8:53875448 | AAACC | A | 45 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
45 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.166-3807_166-3804d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53875448 | ||||||
| chr8:53875449 | AACC | A | 14 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0061 others(11): Show |
14 | HG00609.hp2 HG02074.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.166-3807_166-3805d others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | 53875449 | ||||||
| chr8:53875451 | C | A | 1 | a0001c0001t0006g0043 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.166-3807C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875451 | |||||||
| chr8:53875452 | C | A | 1 | a0001c0001t0001g0204 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.166-3806C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875452 | |||||||
| chr8:53875460 | C | A | 5 | a0001c0001t0002g0165 a0001c0001t0002g0232 a0001c0001t0004g0011 others(2): Show |
5 | HG02004.hp2 HG02723.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-3798C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875460 | |||||||
| chr8:53875691 | T | C | 90 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(87): Show |
90 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.166-3567T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875691 | |||||||
| chr8:53875895 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.166-3363C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53875895 | |||||||
| chr8:53876010 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.166-3248G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53876010 | |||||||
| chr8:53876537 | C | T | 5 | a0001c0001t0002g0117 a0001c0001t0002g0195 a0001c0001t0002g0210 others(2): Show |
5 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-2721C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53876537 | |||||||
| chr8:53876672 | T | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG02055.hp2 HG02572.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.166-2586T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53876672 | |||||||
| chr8:53876755 | G | A | 1 | a0001c0001t0003g0169 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.166-2503G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53876755 | |||||||
| chr8:53877237 | G | T | 58 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(55): Show |
58 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.166-2021G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877237 | |||||||
| chr8:53877268 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.166-1990C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877268 | |||||||
| chr8:53877276 | G | A | 72 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(69): Show |
72 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.166-1982G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877276 | |||||||
| chr8:53877350 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-1908G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877350 | |||||||
| chr8:53877368 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-1890G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877368 | |||||||
| chr8:53877379 | C | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1879C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877379 | |||||||
| chr8:53877380 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1878C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877380 | |||||||
| chr8:53877407 | C | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-1851C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877407 | |||||||
| chr8:53877507 | C | T | 61 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(58): Show |
61 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.166-1751C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877507 | |||||||
| chr8:53877516 | G | T | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.166-1742G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877516 | |||||||
| chr8:53877922 | C | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.166-1336C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53877922 | |||||||
| chr8:53878065 | C | G | 1 | a0001c0001t0004g0037 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.166-1193C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878065 | |||||||
| chr8:53878137 | C | G | 1 | a0001c0001t0002g0134 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.166-1121C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878137 | |||||||
| chr8:53878429 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.166-829C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878429 | |||||||
| chr8:53878461 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.166-797T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878461 | |||||||
| chr8:53878490 | G | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-768G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878490 | |||||||
| chr8:53878737 | G | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-521G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878737 | |||||||
| chr8:53878773 | C | G | 4 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0007g0033 others(1): Show |
4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-485C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878773 | |||||||
| chr8:53878927 | C | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-331C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 1/5 | chr8 | 53878927 | |||||||
| chr8:53879675 | A | G | 19 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0040 others(16): Show |
19 | HG00609.hp2 HG01993.hp1 NA18612.hp2 others(16): Show |
intron_variant | MODIFIER | c.510+73A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53879675 | |||||||
| chr8:53879783 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.510+181G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53879783 | |||||||
| chr8:53879903 | T | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+301T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53879903 | |||||||
| chr8:53879942 | C | A | 1 | a0001c0001t0003g0169 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.510+340C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53879942 | |||||||
| chr8:53879959 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.510+357G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53879959 | |||||||
| chr8:53880299 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.510+697C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53880299 | |||||||
| chr8:53880670 | G | A | 4 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0007g0033 others(1): Show |
4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+1068G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53880670 | |||||||
| chr8:53880675 | G | C | 66 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(63): Show |
66 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.510+1073G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53880675 | |||||||
| chr8:53881024 | G | C | 1 | a0001c0001t0002g0126 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.510+1422G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881024 | |||||||
| chr8:53881176 | G | C | 17 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0001g0093 others(14): Show |
17 | HG00597.hp2 HG00642.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.510+1574G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881176 | |||||||
| chr8:53881223 | C | CCGGTGCG others(19): Show |
1 | a0001c0002t0001g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510+1641_510+1642i others(28): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53881223 | ||||||
| chr8:53881223 | C | CCGGTGCG others(19): Show |
7 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0006 others(4): Show |
7 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+1623_510+1648d others(28): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53881223 | ||||||
| chr8:53881273 | G | C | 1 | a0001c0001t0002g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.510+1671G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881273 | |||||||
| chr8:53881368 | T | C | 86 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(83): Show |
86 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.510+1766T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881368 | |||||||
| chr8:53881437 | C | T | 6 | a0001c0003t0001g0028 a0001c0003t0002g0025 a0001c0003t0002g0029 others(3): Show |
6 | HG02109.hp2 HG02280.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+1835C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881437 | |||||||
| chr8:53881443 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.510+1841G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881443 | |||||||
| chr8:53881552 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510+1950G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881552 | |||||||
| chr8:53881927 | G | A | 2 | a0001c0001t0002g0227 a0001c0001t0002g0228 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.510+2325G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53881927 | |||||||
| chr8:53882151 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.510+2549G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53882151 | |||||||
| chr8:53882450 | T | A | 10 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0002t0001g0005 others(7): Show |
10 | HG02559.hp1 HG02572.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.510+2848T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53882450 | |||||||
| chr8:53882582 | T | C | 5 | a0001c0003t0001g0028 a0001c0003t0002g0025 a0001c0003t0002g0029 others(2): Show |
5 | HG02280.hp2 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+2980T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53882582 | |||||||
| chr8:53882643 | C | CA | 67 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(64): Show |
67 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.510+3059dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53882643 | ||||||
| chr8:53882643 | C | CAA | 8 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0056 others(5): Show |
8 | HG03209.hp1 NA18963.hp2 NA18994.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+3058_510+3059d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53882643 | ||||||
| chr8:53882643 | C | CAAA | 14 | a0001c0001t0001g0010 a0001c0001t0002g0020 a0001c0001t0002g0021 others(11): Show |
14 | HG02109.hp2 HG02559.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.510+3057_510+3059d others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53882643 | ||||||
| chr8:53882643 | C | CAAAA | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0004g0011 others(2): Show |
5 | HG02055.hp2 HG03453.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+3056_510+3059d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53882643 | ||||||
| chr8:53882643 | CA | C | 8 | a0001c0001t0001g0137 a0001c0001t0001g0202 a0001c0001t0001g0229 others(5): Show |
8 | HG00621.hp2 HG01167.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+3059delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53882643 | ||||||
| chr8:53882681 | T | C | 63 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(60): Show |
63 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.510+3079T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53882681 | |||||||
| chr8:53882789 | G | C | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.510+3187G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53882789 | |||||||
| chr8:53883108 | G | T | 85 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(82): Show |
85 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.510+3506G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883108 | |||||||
| chr8:53883157 | C | A | 7 | a0001c0002t0002g0002 a0001c0002t0002g0004 a0001c0002t0002g0006 others(4): Show |
7 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+3555C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883157 | |||||||
| chr8:53883158 | T | A | 1 | a0001c0002t0001g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510+3556T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883158 | |||||||
| chr8:53883158 | T | C | 1 | a0001c0001t0002g0219 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.510+3556T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883158 | |||||||
| chr8:53883160 | T | TC | 61 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(58): Show |
61 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.510+3558_510+3559i others(3): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883160 | |||||||
| chr8:53883275 | G | A | 3 | a0001c0001t0002g0179 a0001c0001t0002g0183 a0001c0001t0008g0114 |
3 | HG02647.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.510+3673G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883275 | |||||||
| chr8:53883444 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.510+3842G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883444 | |||||||
| chr8:53883900 | G | A | 8 | a0001c0002t0001g0005 a0001c0002t0002g0002 a0001c0002t0002g0004 others(5): Show |
8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+4298G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53883900 | |||||||
| chr8:53883946 | C | CA | 68 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(65): Show |
68 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.510+4357dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53883946 | ||||||
| chr8:53884191 | C | CT | 32 | a0001c0001t0001g0018 a0001c0001t0001g0096 a0001c0001t0001g0100 others(29): Show |
32 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.510+4611dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53884191 | ||||||
| chr8:53884191 | C | CTT | 18 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(15): Show |
18 | HG02055.hp2 HG02132.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.510+4610_510+4611d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53884191 | ||||||
| chr8:53884191 | C | CTTT | 46 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(43): Show |
46 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.510+4609_510+4611d others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53884191 | ||||||
| chr8:53884191 | C | CTTTT | 14 | a0001c0001t0001g0023 a0001c0001t0001g0041 a0001c0001t0001g0054 others(11): Show |
14 | HG00438.hp2 HG02027.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.510+4608_510+4611d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53884191 | ||||||
| chr8:53884191 | C | CTTTTT | 8 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0002t0001g0005 others(5): Show |
8 | HG02559.hp1 HG02572.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+4607_510+4611d others(7): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53884191 | ||||||
| chr8:53884191 | CT | C | 6 | a0001c0001t0001g0138 a0001c0001t0001g0185 a0001c0001t0001g0202 others(3): Show |
6 | HG00741.hp2 HG01167.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+4611delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53884191 | ||||||
| chr8:53884230 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.510+4628C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53884230 | |||||||
| chr8:53884392 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.510+4790C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53884392 | |||||||
| chr8:53884642 | A | G | 8 | a0001c0002t0001g0005 a0001c0002t0002g0002 a0001c0002t0002g0004 others(5): Show |
8 | HG02559.hp1 HG02922.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+5040A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53884642 | |||||||
| chr8:53884907 | G | A | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.510+5305G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53884907 | |||||||
| chr8:53885184 | C | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG02572.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+5582C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885184 | |||||||
| chr8:53885244 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.510+5642C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885244 | |||||||
| chr8:53885343 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.510+5741G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885343 | |||||||
| chr8:53885367 | A | G | 63 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(60): Show |
63 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.510+5765A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885367 | |||||||
| chr8:53885502 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0098 |
2 | NA18975.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.510+5900T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885502 | |||||||
| chr8:53885613 | C | CA | 11 | a0001c0001t0001g0121 a0001c0001t0002g0038 a0001c0001t0008g0039 others(8): Show |
11 | HG02027.hp1 HG02559.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+6022dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885613 | ||||||
| chr8:53885736 | A | G | 1 | a0001c0001t0002g0154 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.510+6134A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885736 | |||||||
| chr8:53885790 | C | CT | 18 | a0001c0001t0001g0091 a0001c0001t0001g0120 a0001c0001t0001g0143 others(15): Show |
18 | HG00609.hp1 HG00642.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.510+6210dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | ||||||
| chr8:53885790 | C | CTT | 6 | a0001c0001t0002g0117 a0001c0001t0002g0144 a0001c0001t0002g0195 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+6209_510+6210d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | ||||||
| chr8:53885790 | CT | C | 72 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0031 others(69): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.510+6210delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | ||||||
| chr8:53885790 | CTT | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0035 others(10): Show |
13 | HG01070.hp2 HG01167.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.510+6209_510+6210d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | ||||||
| chr8:53885790 | CTTT | C | 8 | a0001c0002t0001g0005 a0001c0002t0002g0002 a0001c0002t0002g0004 others(5): Show |
8 | HG02109.hp2 HG02559.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+6208_510+6210d others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | ||||||
| chr8:53885790 | CTTTTT | C | 8 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0001t0002g0245 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+6206_510+6210d others(7): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | ||||||
| chr8:53885790 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0002g0168 a0001c0001t0002g0173 |
2 | HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.510+6199_510+6210d others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885790 | ||||||
| chr8:53885887 | TAGAC | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+6289_510+6292d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53885887 | ||||||
| chr8:53885898 | A | T | 59 | a0001c0001t0001g0095 a0001c0001t0001g0105 a0001c0001t0001g0112 others(56): Show |
59 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.510+6296A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53885898 | |||||||
| chr8:53886147 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.510+6545G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53886147 | |||||||
| chr8:53886662 | G | A | 11 | a0001c0001t0002g0170 a0001c0001t0002g0232 a0001c0001t0002g0235 others(8): Show |
11 | HG00741.hp1 HG01109.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.510+7060G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53886662 | |||||||
| chr8:53887100 | C | T | 21 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0242 others(18): Show |
21 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.510+7498C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887100 | |||||||
| chr8:53887110 | T | C | 1 | a0001c0001t0002g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.510+7508T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887110 | |||||||
| chr8:53887164 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.510+7562G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887164 | |||||||
| chr8:53887177 | C | G | 1 | a0001c0001t0002g0209 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.510+7575C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887177 | |||||||
| chr8:53887221 | T | A | 2 | a0001c0001t0002g0243 a0001c0003t0003g0026 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.510+7619T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887221 | |||||||
| chr8:53887489 | G | A | 62 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(59): Show |
62 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.510+7887G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887489 | |||||||
| chr8:53887813 | T | C | 1 | a0001c0001t0009g0128 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.510+8211T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887813 | |||||||
| chr8:53887867 | A | G | 16 | a0001c0001t0001g0041 a0001c0001t0001g0052 a0001c0001t0001g0063 others(13): Show |
16 | HG00438.hp2 HG01496.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.510+8265A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53887867 | |||||||
| chr8:53887978 | TA | T | 9 | a0001c0001t0002g0242 a0001c0002t0001g0005 a0001c0002t0002g0002 others(6): Show |
9 | HG02257.hp2 HG02559.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+8388delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53887978 | ||||||
| chr8:53888219 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.510+8617G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53888219 | |||||||
| chr8:53888767 | T | C | 122 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(119): Show |
122 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.510+9165T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53888767 | |||||||
| chr8:53888886 | C | T | 8 | a0001c0001t0002g0134 a0001c0001t0002g0243 a0001c0001t0002g0244 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+9284C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53888886 | |||||||
| chr8:53888986 | G | A | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.510+9384G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53888986 | |||||||
| chr8:53889223 | T | A | 1 | a0001c0001t0001g0099 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.510+9621T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889223 | |||||||
| chr8:53889242 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.510+9640G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889242 | |||||||
| chr8:53889408 | CTCTCTTT others(9): Show |
C | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.510+9808_510+9823d others(18): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889408 | ||||||
| chr8:53889408 | CTCTCTTT others(12): Show |
C | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+9808_510+9826d others(21): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889408 | ||||||
| chr8:53889412 | C | CT | 27 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0042 others(24): Show |
27 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.510+9849dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | C | CTT | 16 | a0001c0001t0001g0036 a0001c0001t0001g0050 a0001c0001t0001g0055 others(13): Show |
16 | HG01192.hp1 HG02572.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.510+9848_510+9849d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0211 |
2 | HG00621.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.510+9810C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889412 | |||||||
| chr8:53889412 | CT | C | 36 | a0001c0001t0001g0018 a0001c0001t0001g0093 a0001c0001t0001g0095 others(33): Show |
36 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.510+9849delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTT | C | 15 | a0001c0001t0001g0123 a0001c0001t0001g0151 a0001c0001t0001g0180 others(12): Show |
15 | HG00140.hp2 HG01261.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.510+9848_510+9849d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT | C | 21 | a0001c0001t0001g0121 a0001c0001t0001g0254 a0001c0001t0001g0255 others(18): Show |
21 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.510+9843_510+9849d others(9): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0001g0023 a0001c0001t0002g0173 a0001c0001t0002g0176 others(11): Show |
14 | HG02109.hp1 HG02559.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.510+9842_510+9849d others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT others(2): Show |
C | 7 | a0001c0001t0002g0104 a0001c0001t0002g0244 a0001c0001t0002g0246 others(4): Show |
7 | HG01978.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+9841_510+9849d others(11): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0088 a0001c0001t0001g0225 others(1): Show |
4 | HG02074.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+9840_510+9849d others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT others(4): Show |
C | 14 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0098 others(11): Show |
14 | HG00642.hp2 HG01099.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.510+9839_510+9849d others(13): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT others(5): Show |
C | 7 | a0001c0001t0001g0101 a0001c0001t0001g0110 a0001c0001t0001g0193 others(4): Show |
7 | HG00609.hp1 HG02895.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+9838_510+9849d others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT others(6): Show |
C | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0038 others(2): Show |
5 | HG02055.hp2 HG02809.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+9837_510+9849d others(15): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT others(7): Show |
C | 4 | a0001c0001t0002g0242 a0001c0001t0004g0037 a0001c0001t0006g0043 others(1): Show |
4 | HG01069.hp2 HG01167.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+9836_510+9849d others(16): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0007g0045 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.510+9835_510+9849d others(17): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT others(9): Show |
C | 15 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0074 others(12): Show |
15 | HG01070.hp2 HG01496.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.510+9834_510+9849d others(18): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.510+9833_510+9849d others(19): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0002g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.510+9832_510+9849d others(20): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889412 | CTTTTTTT others(16): Show |
C | 2 | a0001c0001t0003g0001 a0001c0002t0003g0003 |
2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.510+9827_510+9849d others(25): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889412 | ||||||
| chr8:53889414 | T | C | 4 | a0001c0001t0002g0146 a0001c0001t0002g0157 a0001c0001t0002g0159 others(1): Show |
4 | HG01358.hp2 HG03239.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+9812T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889414 | |||||||
| chr8:53889415 | T | C | 2 | a0001c0001t0001g0200 a0001c0001t0002g0212 |
2 | HG03688.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.510+9813T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889415 | |||||||
| chr8:53889420 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.510+9818T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889420 | |||||||
| chr8:53889421 | T | C | 20 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0002g0032 others(17): Show |
20 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.510+9819T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889421 | |||||||
| chr8:53889422 | T | C | 12 | a0001c0001t0001g0023 a0001c0001t0002g0132 a0001c0001t0002g0173 others(9): Show |
12 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.510+9820T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889422 | |||||||
| chr8:53889423 | T | C | 22 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0002g0032 others(19): Show |
22 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.510+9821T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889423 | |||||||
| chr8:53889424 | T | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0002g0132 others(10): Show |
13 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.510+9822T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889424 | |||||||
| chr8:53889425 | T | C | 23 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0002g0032 others(20): Show |
23 | HG01192.hp2 HG01243.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.510+9823T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889425 | |||||||
| chr8:53889426 | T | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0002g0016 others(12): Show |
15 | HG02109.hp1 HG02559.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.510+9824T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889426 | |||||||
| chr8:53889427 | T | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0038 others(5): Show |
8 | HG02055.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+9825T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889427 | |||||||
| chr8:53889428 | T | C | 8 | a0001c0001t0001g0010 a0001c0001t0002g0016 a0001c0001t0002g0242 others(5): Show |
8 | HG01069.hp2 HG01167.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+9826T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889428 | |||||||
| chr8:53889429 | T | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0038 others(3): Show |
6 | HG01071.hp2 HG02055.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+9827T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889429 | |||||||
| chr8:53889430 | T | C | 19 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0074 others(16): Show |
19 | HG01069.hp2 HG01070.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.510+9828T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889430 | |||||||
| chr8:53889431 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0007g0045 |
2 | HG01071.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.510+9829T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889431 | |||||||
| chr8:53889432 | T | C | 15 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0074 others(12): Show |
15 | HG01070.hp2 HG01496.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.510+9830T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889432 | |||||||
| chr8:53889433 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.510+9831T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889433 | |||||||
| chr8:53889434 | T | C | 14 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0074 others(11): Show |
14 | HG01496.hp2 HG02132.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.510+9832T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889434 | |||||||
| chr8:53889435 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.510+9833T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889435 | |||||||
| chr8:53889504 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510+9902C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889504 | |||||||
| chr8:53889574 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.510+9972G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889574 | |||||||
| chr8:53889645 | C | T | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+10043C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889645 | |||||||
| chr8:53889646 | G | A | 2 | a0001c0001t0002g0094 a0001c0001t0002g0134 |
2 | HG00597.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.510+10044G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889646 | |||||||
| chr8:53889723 | C | CTGTGTGT others(1): Show |
6 | a0001c0001t0011g0208 a0001c0002t0002g0002 a0001c0002t0002g0004 others(3): Show |
6 | HG02109.hp1 HG02559.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+10148_510+1015 others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889723 | ||||||
| chr8:53889723 | CTG | C | 171 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0035 others(168): Show |
171 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.510+10154_510+1015 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889723 | ||||||
| chr8:53889723 | CTGTG | C | 25 | a0001c0001t0001g0010 a0001c0001t0001g0072 a0001c0001t0001g0096 others(22): Show |
25 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.510+10152_510+1015 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889723 | ||||||
| chr8:53889723 | CTGTGTG | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0002g0016 others(10): Show |
13 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.510+10150_510+1015 others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53889723 | ||||||
| chr8:53889771 | TCTC | T | 3 | a0001c0001t0002g0038 a0001c0001t0004g0037 a0001c0001t0008g0039 |
3 | HG01167.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.510+10170_510+1017 others(7): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889771 | |||||||
| chr8:53889818 | T | G | 1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.510+10216T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889818 | |||||||
| chr8:53889850 | G | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0130 a0001c0001t0001g0137 others(6): Show |
9 | HG00408.hp2 HG00621.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+10248G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889850 | |||||||
| chr8:53889880 | C | T | 2 | a0001c0001t0002g0021 a0001c0001t0003g0030 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+10278C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889880 | |||||||
| chr8:53889997 | G | A | 1 | a0001c0001t0002g0245 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.510+10395G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53889997 | |||||||
| chr8:53890216 | T | G | 9 | a0001c0001t0002g0021 a0001c0001t0003g0030 a0001c0001t0011g0208 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+10614T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53890216 | |||||||
| chr8:53890220 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.510+10618C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53890220 | |||||||
| chr8:53890354 | A | G | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.510+10752A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53890354 | |||||||
| chr8:53890971 | G | A | 6 | a0001c0001t0001g0180 a0001c0001t0001g0200 a0001c0001t0002g0019 others(3): Show |
6 | NA18946.hp2 NA18952.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+11369G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53890971 | |||||||
| chr8:53891560 | G | T | 46 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0072 others(43): Show |
46 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.510+11958G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53891560 | |||||||
| chr8:53891732 | T | C | 2 | a0001c0001t0002g0021 a0001c0001t0003g0030 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+12130T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53891732 | |||||||
| chr8:53891888 | T | A | 4 | a0001c0001t0002g0145 a0001c0001t0002g0150 a0001c0001t0002g0156 others(1): Show |
4 | HG00140.hp2 HG01123.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+12286T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53891888 | |||||||
| chr8:53892242 | A | G | 1 | a0001c0001t0003g0169 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.510+12640A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892242 | |||||||
| chr8:53892307 | T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+12705T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892307 | |||||||
| chr8:53892489 | T | C | 2 | a0001c0001t0002g0021 a0001c0001t0003g0030 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+12887T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892489 | |||||||
| chr8:53892595 | A | T | 1 | a0001c0001t0002g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.510+12993A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892595 | |||||||
| chr8:53892652 | T | C | 7 | a0001c0001t0011g0208 a0001c0002t0001g0005 a0001c0002t0002g0002 others(4): Show |
7 | HG02109.hp1 HG02559.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+13050T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892652 | |||||||
| chr8:53892919 | A | G | 2 | a0001c0001t0002g0021 a0001c0001t0003g0030 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+13317A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892919 | |||||||
| chr8:53892983 | C | T | 41 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0063 others(38): Show |
41 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+13381C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53892983 | |||||||
| chr8:53893013 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(5): Show |
8 | HG02055.hp2 HG02886.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.510+13411G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893013 | |||||||
| chr8:53893079 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0091 |
2 | HG02027.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.510+13477A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893079 | |||||||
| chr8:53893475 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.510+13873G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893475 | |||||||
| chr8:53893621 | A | G | 65 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(62): Show |
65 | HG01069.hp2 HG01167.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.510+14019A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893621 | |||||||
| chr8:53893822 | T | G | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.510+14220T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893822 | |||||||
| chr8:53893883 | G | A | 1 | a0001c0002t0001g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510+14281G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893883 | |||||||
| chr8:53893898 | G | A | 1 | a0001c0001t0010g0189 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.510+14296G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893898 | |||||||
| chr8:53893968 | T | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0085 |
2 | NA18955.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.510+14366T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53893968 | |||||||
| chr8:53893993 | GA | G | 44 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(41): Show |
44 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.510+14395delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53893993 | ||||||
| chr8:53894075 | T | C | 2 | a0001c0001t0002g0021 a0001c0001t0003g0030 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+14473T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894075 | |||||||
| chr8:53894206 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.510+14604A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894206 | |||||||
| chr8:53894222 | A | G | 38 | a0001c0001t0001g0052 a0001c0001t0001g0063 a0001c0001t0001g0074 others(35): Show |
38 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(35): Show |
intron_variant | MODIFIER | c.510+14620A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894222 | |||||||
| chr8:53894402 | T | C | 65 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(62): Show |
65 | HG01069.hp2 HG01167.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.510+14800T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894402 | |||||||
| chr8:53894488 | C | A | 51 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0063 others(48): Show |
51 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(48): Show |
intron_variant | MODIFIER | c.510+14886C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894488 | |||||||
| chr8:53894488 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.510+14886C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894488 | |||||||
| chr8:53894624 | A | G | 65 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(62): Show |
65 | HG01069.hp2 HG01167.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.510+15022A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894624 | |||||||
| chr8:53894729 | A | G | 5 | a0001c0001t0001g0143 a0001c0001t0005g0118 a0001c0001t0005g0119 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+15127A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894729 | |||||||
| chr8:53894988 | A | G | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.510+15386A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53894988 | |||||||
| chr8:53895016 | A | G | 1 | a0001c0001t0002g0179 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.510+15414A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895016 | |||||||
| chr8:53895072 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.510+15470A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895072 | |||||||
| chr8:53895127 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.510+15525G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895127 | |||||||
| chr8:53895203 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.510+15601T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895203 | |||||||
| chr8:53895558 | A | G | 50 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0063 others(47): Show |
50 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.510+15956A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895558 | |||||||
| chr8:53895594 | C | T | 41 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0063 others(38): Show |
41 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+15992C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895594 | |||||||
| chr8:53895713 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510+16111C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895713 | |||||||
| chr8:53895938 | C | T | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+16336C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895938 | |||||||
| chr8:53895988 | G | C | 255 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(252): Show |
255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.510+16386G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53895988 | |||||||
| chr8:53896246 | C | T | 50 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0063 others(47): Show |
50 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.510+16644C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53896246 | |||||||
| chr8:53896283 | C | A | 1 | a0001c0001t0002g0184 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.510+16681C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53896283 | |||||||
| chr8:53896679 | A | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0067 |
2 | NA18954.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.510+17077A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53896679 | |||||||
| chr8:53897214 | C | G | 50 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0063 others(47): Show |
50 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.510+17612C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897214 | |||||||
| chr8:53897432 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+17830C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897432 | |||||||
| chr8:53897495 | C | A | 3 | a0001c0001t0002g0038 a0001c0001t0004g0037 a0001c0001t0008g0039 |
3 | HG01167.hp1 HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.510+17893C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897495 | |||||||
| chr8:53897519 | A | G | 50 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0063 others(47): Show |
50 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.510+17917A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897519 | |||||||
| chr8:53897607 | T | C | 65 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(62): Show |
65 | HG01069.hp2 HG01167.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.510+18005T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897607 | |||||||
| chr8:53897890 | G | A | 41 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0063 others(38): Show |
41 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+18288G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897890 | |||||||
| chr8:53897891 | C | T | 50 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0063 others(47): Show |
50 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.510+18289C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897891 | |||||||
| chr8:53897921 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.510+18319G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53897921 | |||||||
| chr8:53898033 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.510+18431C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898033 | |||||||
| chr8:53898101 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.510+18499G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898101 | |||||||
| chr8:53898101 | G | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(12): Show |
15 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.510+18499G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898101 | |||||||
| chr8:53898104 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.510+18502C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898104 | |||||||
| chr8:53898111 | C | T | 2 | a0001c0001t0002g0021 a0001c0001t0003g0030 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+18509C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898111 | |||||||
| chr8:53898132 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.510+18530T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898132 | |||||||
| chr8:53898373 | T | A | 41 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0063 others(38): Show |
41 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(38): Show |
intron_variant | MODIFIER | c.510+18771T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898373 | |||||||
| chr8:53898631 | A | G | 7 | a0001c0001t0011g0208 a0001c0002t0001g0005 a0001c0002t0002g0002 others(4): Show |
7 | HG02109.hp1 HG02559.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+19029A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898631 | |||||||
| chr8:53898828 | G | A | 65 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(62): Show |
65 | HG01069.hp2 HG01167.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.510+19226G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53898828 | |||||||
| chr8:53899092 | C | T | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.510+19490C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899092 | |||||||
| chr8:53899093 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.510+19491C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899093 | |||||||
| chr8:53899307 | G | A | 1 | a0001c0001t0003g0236 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.510+19705G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899307 | |||||||
| chr8:53899388 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.510+19786G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899388 | |||||||
| chr8:53899766 | A | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(8): Show |
11 | HG01167.hp1 HG02055.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+20164A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899766 | |||||||
| chr8:53899819 | G | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+20217G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899819 | |||||||
| chr8:53899861 | A | T | 1 | a0001c0001t0002g0017 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.510+20259A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899861 | |||||||
| chr8:53899908 | C | T | 64 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0063 others(61): Show |
64 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(61): Show |
intron_variant | MODIFIER | c.510+20306C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53899908 | |||||||
| chr8:53900028 | C | T | 1 | a0001c0001t0002g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.510+20426C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900028 | |||||||
| chr8:53900152 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0105 |
2 | NA18961.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.510+20550A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900152 | |||||||
| chr8:53900234 | TG | T | 3 | a0001c0001t0001g0023 a0001c0001t0003g0022 a0001c0001t0003g0024 |
3 | HG02886.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.510+20635delG | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53900234 | ||||||
| chr8:53900254 | A | G | 12 | a0001c0001t0002g0020 a0001c0001t0002g0170 a0001c0001t0002g0232 others(9): Show |
12 | HG00741.hp1 HG01109.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.510+20652A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900254 | |||||||
| chr8:53900799 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.510+21197T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900799 | |||||||
| chr8:53900887 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.510+21285C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900887 | |||||||
| chr8:53900889 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.510+21287C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900889 | |||||||
| chr8:53900985 | A | G | 70 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(67): Show |
70 | HG01069.hp2 HG01167.hp1 HG01192.hp2 others(67): Show |
intron_variant | MODIFIER | c.510+21383A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53900985 | |||||||
| chr8:53901062 | C | CT | 6 | a0001c0001t0001g0018 a0001c0001t0001g0225 a0001c0001t0001g0230 others(3): Show |
6 | HG01069.hp2 HG02074.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+21479dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53901062 | ||||||
| chr8:53901062 | CT | C | 51 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0063 others(48): Show |
51 | HG01071.hp2 HG01167.hp2 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.510+21479delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53901062 | ||||||
| chr8:53901062 | CTT | C | 5 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0002g0021 others(2): Show |
5 | HG01070.hp2 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+21478_510+2147 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53901062 | ||||||
| chr8:53901193 | G | A | 4 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0007g0033 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+21591G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901193 | |||||||
| chr8:53901360 | G | A | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.510+21758G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901360 | |||||||
| chr8:53901547 | T | A | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.510+21945T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901547 | |||||||
| chr8:53901614 | A | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.510+22012A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901614 | |||||||
| chr8:53901719 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.510+22117C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901719 | |||||||
| chr8:53901725 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0202 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.510+22123T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901725 | |||||||
| chr8:53901821 | G | GCACTC | 4 | a0001c0001t0002g0021 a0001c0001t0003g0030 a0001c0001t0005g0118 others(1): Show |
4 | HG02055.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+22224_510+2222 others(9): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53901821 | ||||||
| chr8:53901870 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0061 |
2 | HG02698.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.510+22268A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53901870 | |||||||
| chr8:53902081 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.510+22479G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902081 | |||||||
| chr8:53902104 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.510+22502G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902104 | |||||||
| chr8:53902246 | C | T | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+22644C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902246 | |||||||
| chr8:53902252 | G | C | 1 | a0001c0001t0002g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.510+22650G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902252 | |||||||
| chr8:53902385 | A | G | 79 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(76): Show |
79 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.510+22783A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902385 | |||||||
| chr8:53902443 | A | G | 24 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(21): Show |
24 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.510+22841A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902443 | |||||||
| chr8:53902526 | A | G | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+22924A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902526 | |||||||
| chr8:53902562 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+22960C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902562 | |||||||
| chr8:53902575 | A | G | 24 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(21): Show |
24 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.510+22973A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902575 | |||||||
| chr8:53902631 | T | C | 1 | a0001c0001t0002g0155 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.510+23029T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902631 | |||||||
| chr8:53902731 | C | CT | 62 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(59): Show |
62 | HG00741.hp1 HG01192.hp2 HG01243.hp2 others(59): Show |
intron_variant | MODIFIER | c.510+23140dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53902731 | ||||||
| chr8:53902788 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+23186C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902788 | |||||||
| chr8:53902808 | C | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG01069.hp1 HG01071.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.510+23206C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902808 | |||||||
| chr8:53902818 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0004g0037 |
2 | HG01167.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.510+23216C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902818 | |||||||
| chr8:53902853 | G | A | 55 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(52): Show |
55 | HG00741.hp1 HG01192.hp2 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.510+23251G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902853 | |||||||
| chr8:53902887 | G | A | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+23285G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902887 | |||||||
| chr8:53902960 | G | A | 55 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(52): Show |
55 | HG00741.hp1 HG01192.hp2 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.510+23358G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902960 | |||||||
| chr8:53902979 | A | G | 79 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(76): Show |
79 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.510+23377A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53902979 | |||||||
| chr8:53903018 | T | C | 255 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(252): Show |
255 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.510+23416T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53903018 | |||||||
| chr8:53903241 | T | C | 79 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(76): Show |
79 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.510+23639T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53903241 | |||||||
| chr8:53903269 | G | A | 79 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(76): Show |
79 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(76): Show |
intron_variant | MODIFIER | c.510+23667G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53903269 | |||||||
| chr8:53903883 | G | A | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+24281G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53903883 | |||||||
| chr8:53903884 | C | T | 1 | a0001c0001t0008g0114 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.510+24282C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53903884 | |||||||
| chr8:53903938 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.510+24336G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53903938 | |||||||
| chr8:53904011 | T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+24409T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904011 | |||||||
| chr8:53904018 | G | A | 4 | a0001c0001t0002g0243 a0001c0003t0001g0028 a0001c0003t0003g0026 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+24416G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904018 | |||||||
| chr8:53904061 | A | G | 18 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(15): Show |
18 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.510+24459A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904061 | |||||||
| chr8:53904126 | CT | C | 5 | a0001c0001t0001g0080 a0001c0001t0001g0197 a0001c0001t0002g0170 others(2): Show |
5 | HG01168.hp2 HG02132.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+24540delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53904126 | ||||||
| chr8:53904126 | CTT | C | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+24539_510+2454 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53904126 | ||||||
| chr8:53904126 | CTTT | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(15): Show |
18 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.510+24538_510+2454 others(7): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53904126 | ||||||
| chr8:53904352 | G | A | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.510+24750G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904352 | |||||||
| chr8:53904424 | A | G | 24 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(21): Show |
24 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.510+24822A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904424 | |||||||
| chr8:53904589 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.510+24987T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904589 | |||||||
| chr8:53904599 | T | C | 24 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(21): Show |
24 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.510+24997T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904599 | |||||||
| chr8:53904763 | TAATA | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+25164_510+2516 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53904763 | ||||||
| chr8:53904863 | T | G | 24 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(21): Show |
24 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.510+25261T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904863 | |||||||
| chr8:53904971 | A | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0004g0037 others(1): Show |
4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+25369A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53904971 | |||||||
| chr8:53905026 | C | T | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+25424C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53905026 | |||||||
| chr8:53905188 | T | C | 55 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(52): Show |
55 | HG00741.hp1 HG01192.hp2 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.510+25586T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53905188 | |||||||
| chr8:53905231 | A | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0004g0037 others(1): Show |
4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+25629A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53905231 | |||||||
| chr8:53905886 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.510+26284C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53905886 | |||||||
| chr8:53905997 | G | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+26395G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53905997 | |||||||
| chr8:53906024 | G | A | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+26422G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906024 | |||||||
| chr8:53906077 | C | T | 4 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0006g0043 others(1): Show |
4 | HG01069.hp2 HG02055.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+26475C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906077 | |||||||
| chr8:53906172 | T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+26570T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906172 | |||||||
| chr8:53906213 | A | G | 23 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(20): Show |
23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.510+26611A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906213 | |||||||
| chr8:53906259 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+26657C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906259 | |||||||
| chr8:53906425 | G | A | 4 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0004g0037 others(1): Show |
4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+26823G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906425 | |||||||
| chr8:53906431 | C | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+26829C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906431 | |||||||
| chr8:53906442 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510+26840T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906442 | |||||||
| chr8:53906737 | T | C | 23 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(20): Show |
23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.510+27135T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906737 | |||||||
| chr8:53906773 | A | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+27171A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906773 | |||||||
| chr8:53906793 | C | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+27191C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53906793 | |||||||
| chr8:53907181 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.510+27579C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907181 | |||||||
| chr8:53907229 | C | T | 4 | a0001c0001t0002g0243 a0001c0003t0001g0028 a0001c0003t0003g0026 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+27627C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907229 | |||||||
| chr8:53907240 | T | C | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+27638T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907240 | |||||||
| chr8:53907353 | G | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+27751G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907353 | |||||||
| chr8:53907413 | G | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+27811G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907413 | |||||||
| chr8:53907509 | A | G | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+27907A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907509 | |||||||
| chr8:53907587 | G | GA | 31 | a0001c0001t0002g0020 a0001c0001t0002g0108 a0001c0001t0002g0117 others(28): Show |
31 | HG01109.hp2 HG01192.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.510+27996dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53907587 | ||||||
| chr8:53907587 | G | GAA | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+27995_510+2799 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53907587 | ||||||
| chr8:53907702 | G | GCTAA | 5 | a0001c0001t0002g0243 a0001c0001t0003g0030 a0001c0003t0001g0028 others(2): Show |
5 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+28102_510+2810 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53907702 | ||||||
| chr8:53907722 | C | T | 1 | a0001c0002t0003g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.510+28120C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907722 | |||||||
| chr8:53907742 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.510+28140G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907742 | |||||||
| chr8:53907841 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510+28239C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907841 | |||||||
| chr8:53907889 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.510+28287T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907889 | |||||||
| chr8:53907955 | G | GA | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.510+28359dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53907955 | ||||||
| chr8:53907965 | A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510+28363A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53907965 | |||||||
| chr8:53908184 | G | C | 1 | a0001c0001t0002g0258 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.510+28582G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53908184 | |||||||
| chr8:53908259 | G | C | 4 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0004g0037 others(1): Show |
4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+28657G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53908259 | |||||||
| chr8:53908298 | T | C | 23 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(20): Show |
23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.510+28696T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53908298 | |||||||
| chr8:53908404 | C | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0098 |
2 | NA18975.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.510+28802C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53908404 | |||||||
| chr8:53908513 | G | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+28911G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53908513 | |||||||
| chr8:53908632 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0123 |
2 | NA18945.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.510+29030C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53908632 | |||||||
| chr8:53908640 | C | CA | 109 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(106): Show |
109 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.510+29051dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53908640 | ||||||
| chr8:53909203 | ATG | A | 4 | a0001c0001t0002g0171 a0001c0001t0002g0194 a0001c0001t0002g0203 others(1): Show |
4 | HG01192.hp2 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+29607_510+2960 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909203 | ||||||
| chr8:53909207 | G | GTGTGTA | 5 | a0001c0001t0001g0015 a0001c0001t0002g0016 a0001c0001t0005g0118 others(2): Show |
5 | HG02055.hp1 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+29608_510+2960 others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | ||||||
| chr8:53909207 | GTGTA | G | 10 | a0001c0001t0001g0121 a0001c0001t0001g0185 a0001c0001t0001g0213 others(7): Show |
10 | HG02027.hp1 HG02083.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.510+29607_510+2961 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | ||||||
| chr8:53909207 | GTGTATA | G | 20 | a0001c0001t0001g0081 a0001c0001t0002g0020 a0001c0001t0002g0146 others(17): Show |
20 | HG00140.hp2 HG01109.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.510+29607_510+2961 others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | ||||||
| chr8:53909207 | GTGTATAT others(1): Show |
G | 27 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0075 others(24): Show |
27 | HG00741.hp1 HG01123.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.510+29607_510+2961 others(12): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | ||||||
| chr8:53909207 | GTGTATAT others(3): Show |
G | 36 | a0001c0001t0001g0055 a0001c0001t0001g0063 a0001c0001t0001g0072 others(33): Show |
36 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.510+29607_510+2961 others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | ||||||
| chr8:53909207 | GTGTATAT others(5): Show |
G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0080 others(4): Show |
7 | HG01243.hp2 HG02132.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+29607_510+2961 others(16): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | ||||||
| chr8:53909207 | GTGTATAT others(21): Show |
G | 1 | a0001c0001t0002g0134 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.510+29607_510+2963 others(32): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | ||||||
| chr8:53909207 | GTGTATAT others(23): Show |
G | 4 | a0001c0001t0002g0243 a0001c0003t0001g0028 a0001c0003t0003g0026 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+29607_510+2963 others(34): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | ||||||
| chr8:53909207 | GTGTATAT others(25): Show |
G | 2 | a0001c0001t0002g0021 a0001c0001t0003g0030 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.510+29607_510+2963 others(36): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909207 | ||||||
| chr8:53909209 | G | A | 5 | a0001c0001t0001g0068 a0001c0001t0001g0160 a0001c0001t0002g0156 others(2): Show |
5 | HG01346.hp1 HG02165.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+29607G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909209 | |||||||
| chr8:53909209 | G | GTA | 12 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0093 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.510+29652_510+2965 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909209 | G | GTGTA | 6 | a0001c0001t0001g0010 a0001c0001t0002g0246 a0001c0001t0004g0011 others(3): Show |
6 | HG01069.hp2 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.510+29608_510+2960 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909209 | G | GTGTATGT others(3): Show |
1 | a0001c0001t0001g0143 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510+29608_510+2960 others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909209 | GTA | G | 45 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0035 others(42): Show |
45 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.510+29652_510+2965 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909209 | GTATA | G | 18 | a0001c0001t0001g0092 a0001c0001t0001g0101 a0001c0001t0001g0112 others(15): Show |
18 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.510+29650_510+2965 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909209 | GTATATA | G | 19 | a0001c0001t0001g0018 a0001c0001t0001g0058 a0001c0001t0001g0095 others(16): Show |
19 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.510+29648_510+2965 others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909209 | GTATATAT others(3): Show |
G | 1 | a0001c0001t0007g0033 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.510+29644_510+2965 others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909209 | GTATATAT others(5): Show |
G | 1 | a0001c0001t0007g0045 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.510+29642_510+2965 others(16): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909209 | GTATATAT others(7): Show |
G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0105 a0001c0001t0001g0200 others(1): Show |
4 | HG03688.hp2 NA18988.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+29640_510+2965 others(18): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909209 | GTATATAT others(11): Show |
G | 2 | a0001c0001t0009g0136 a0001c0003t0002g0029 |
2 | HG02886.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.510+29636_510+2965 others(22): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909209 | GTATATAT others(13): Show |
G | 1 | a0001c0001t0001g0191 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.510+29634_510+2965 others(24): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909209 | GTATATAT others(15): Show |
G | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.510+29632_510+2965 others(26): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909209 | GTATATAT others(19): Show |
G | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.510+29628_510+2965 others(30): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53909209 | ||||||
| chr8:53909211 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0002g0246 a0001c0001t0004g0011 others(5): Show |
8 | HG01069.hp2 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.510+29609A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909211 | |||||||
| chr8:53909213 | A | G | 5 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0002g0248 others(2): Show |
5 | HG01074.hp2 HG01167.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.510+29611A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909213 | |||||||
| chr8:53909217 | A | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0004g0037 others(1): Show |
4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+29615A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909217 | |||||||
| chr8:53909229 | A | G | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+29627A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909229 | |||||||
| chr8:53909233 | A | G | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+29631A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909233 | |||||||
| chr8:53909254 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.510+29652T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909254 | |||||||
| chr8:53909255 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.510+29653A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909255 | |||||||
| chr8:53909256 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.510+29654C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909256 | |||||||
| chr8:53909302 | A | T | 23 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(20): Show |
23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.510+29700A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909302 | |||||||
| chr8:53909347 | T | C | 1 | a0001c0001t0002g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.510+29745T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909347 | |||||||
| chr8:53909428 | T | G | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510+29826T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909428 | |||||||
| chr8:53909445 | T | C | 23 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(20): Show |
23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.510+29843T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909445 | |||||||
| chr8:53909456 | A | G | 23 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(20): Show |
23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.510+29854A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909456 | |||||||
| chr8:53909530 | AG | A | 4 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0004g0037 others(1): Show |
4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+29929delG | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909530 | |||||||
| chr8:53909554 | C | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(12): Show |
15 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.510+29952C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909554 | |||||||
| chr8:53909577 | C | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.510+29975C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909577 | |||||||
| chr8:53909600 | T | C | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.511-29976T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909600 | |||||||
| chr8:53909616 | T | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-29960T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909616 | |||||||
| chr8:53909759 | G | A | 133 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(130): Show |
133 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.511-29817G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53909759 | |||||||
| chr8:53910277 | CA | C | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-29291delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53910277 | ||||||
| chr8:53910421 | GA | G | 109 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(106): Show |
109 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.511-29145delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53910421 | ||||||
| chr8:53910422 | AAAAAAAA others(3): Show |
A | 1 | a0001c0003t0004g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.511-29153_511-2914 others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910422 | |||||||
| chr8:53910469 | T | C | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-29107T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910469 | |||||||
| chr8:53910505 | A | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(6): Show |
9 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.511-29071A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910505 | |||||||
| chr8:53910507 | G | T | 1 | a0001c0001t0002g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.511-29069G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910507 | |||||||
| chr8:53910666 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-28910C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910666 | |||||||
| chr8:53910748 | G | A | 133 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(130): Show |
133 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.511-28828G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910748 | |||||||
| chr8:53910873 | A | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0004g0037 others(1): Show |
4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-28703A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53910873 | |||||||
| chr8:53911215 | C | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-28361C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911215 | |||||||
| chr8:53911241 | G | C | 23 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(20): Show |
23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.511-28335G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911241 | |||||||
| chr8:53911330 | C | A | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-28246C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911330 | |||||||
| chr8:53911413 | G | A | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-28163G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911413 | |||||||
| chr8:53911459 | T | A | 1 | a0001c0001t0002g0226 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.511-28117T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911459 | |||||||
| chr8:53911503 | C | T | 23 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(20): Show |
23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.511-28073C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911503 | |||||||
| chr8:53911562 | T | TTG | 133 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(130): Show |
133 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.511-28014_511-2801 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911562 | |||||||
| chr8:53911594 | G | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-27982G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911594 | |||||||
| chr8:53911606 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.511-27970G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911606 | |||||||
| chr8:53911619 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511-27957G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911619 | |||||||
| chr8:53911732 | G | A | 1 | a0001c0001t0002g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511-27844G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53911732 | |||||||
| chr8:53912144 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0256 |
2 | NA18612.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.511-27432A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53912144 | |||||||
| chr8:53912234 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0003g0024 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.511-27342A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53912234 | |||||||
| chr8:53912352 | A | AT | 17 | a0001c0001t0001g0010 a0001c0001t0001g0142 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02273.hp2 others(14): Show |
intron_variant | MODIFIER | c.511-27207dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53912352 | ||||||
| chr8:53912352 | AT | A | 166 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(163): Show |
166 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.511-27207delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53912352 | ||||||
| chr8:53912575 | A | G | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-27001A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53912575 | |||||||
| chr8:53912595 | C | T | 109 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(106): Show |
109 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.511-26981C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53912595 | |||||||
| chr8:53912970 | A | AT | 5 | a0001c0001t0001g0015 a0001c0001t0002g0149 a0001c0001t0002g0226 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-26593dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53912970 | ||||||
| chr8:53913352 | G | A | 109 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(106): Show |
109 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.511-26224G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53913352 | |||||||
| chr8:53913352 | G | T | 23 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(20): Show |
23 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.511-26224G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53913352 | |||||||
| chr8:53913403 | G | A | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-26173G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53913403 | |||||||
| chr8:53913577 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.511-25999G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53913577 | |||||||
| chr8:53913773 | C | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-25803C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53913773 | |||||||
| chr8:53914037 | C | CT | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-25528dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53914037 | ||||||
| chr8:53914037 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-25536_511-2552 others(13): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53914037 | ||||||
| chr8:53914037 | C | CTTTTTTT others(3): Show |
7 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0002g0170 others(4): Show |
7 | HG02451.hp2 HG02602.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-25537_511-2552 others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53914037 | ||||||
| chr8:53914037 | C | CTTTTTTT others(4): Show |
99 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0060 others(96): Show |
99 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.511-25538_511-2552 others(15): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53914037 | ||||||
| chr8:53914037 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0063 a0001c0001t0001g0068 a0001c0001t0001g0160 |
3 | HG02165.hp1 NA18612.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.511-25528_511-2552 others(16): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53914037 | ||||||
| chr8:53914199 | T | C | 1 | a0001c0001t0003g0234 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.511-25377T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914199 | |||||||
| chr8:53914255 | T | C | 40 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0063 others(37): Show |
40 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(37): Show |
intron_variant | MODIFIER | c.511-25321T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914255 | |||||||
| chr8:53914285 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-25291C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914285 | |||||||
| chr8:53914344 | G | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-25232G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914344 | |||||||
| chr8:53914422 | C | A | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-25154C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914422 | |||||||
| chr8:53914480 | T | A | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-25096T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914480 | |||||||
| chr8:53914557 | A | G | 1 | a0001c0001t0002g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.511-25019A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914557 | |||||||
| chr8:53914599 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.511-24977G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914599 | |||||||
| chr8:53914783 | C | T | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-24793C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914783 | |||||||
| chr8:53914841 | A | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-24735A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914841 | |||||||
| chr8:53914842 | A | T | 135 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(132): Show |
135 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.511-24734A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914842 | |||||||
| chr8:53914872 | C | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-24704C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914872 | |||||||
| chr8:53914880 | C | T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-24696C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914880 | |||||||
| chr8:53914976 | A | C | 42 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(39): Show |
42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-24600A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53914976 | |||||||
| chr8:53915017 | C | G | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-24559C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915017 | |||||||
| chr8:53915032 | T | C | 42 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(39): Show |
42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-24544T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915032 | |||||||
| chr8:53915077 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.511-24499G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915077 | |||||||
| chr8:53915100 | C | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-24476C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915100 | |||||||
| chr8:53915116 | G | C | 1 | a0001c0001t0002g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.511-24460G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915116 | |||||||
| chr8:53915144 | C | CA | 131 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0052 others(128): Show |
131 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.511-24417dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53915144 | ||||||
| chr8:53915144 | CA | C | 51 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0058 others(48): Show |
51 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.511-24417delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53915144 | ||||||
| chr8:53915232 | G | A | 1 | a0001c0001t0003g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.511-24344G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915232 | |||||||
| chr8:53915289 | C | T | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-24287C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915289 | |||||||
| chr8:53915307 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.511-24269G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915307 | |||||||
| chr8:53915347 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.511-24229G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915347 | |||||||
| chr8:53915378 | T | C | 15 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(12): Show |
15 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.511-24198T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915378 | |||||||
| chr8:53915403 | G | T | 42 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(39): Show |
42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-24173G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915403 | |||||||
| chr8:53915642 | G | C | 59 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(56): Show |
59 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.511-23934G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915642 | |||||||
| chr8:53915795 | C | T | 42 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(39): Show |
42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-23781C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915795 | |||||||
| chr8:53915834 | A | G | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-23742A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915834 | |||||||
| chr8:53915854 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.511-23722G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53915854 | |||||||
| chr8:53916037 | A | T | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.511-23539A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53916037 | |||||||
| chr8:53916158 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.511-23418G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53916158 | |||||||
| chr8:53916427 | A | AT | 10 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0096 others(7): Show |
10 | HG00741.hp2 HG02155.hp2 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.511-23144dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53916427 | ||||||
| chr8:53916763 | C | T | 42 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(39): Show |
42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-22813C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53916763 | |||||||
| chr8:53916949 | C | G | 1 | a0001c0003t0003g0026 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.511-22627C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53916949 | |||||||
| chr8:53917092 | A | G | 73 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(70): Show |
73 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.511-22484A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917092 | |||||||
| chr8:53917122 | C | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-22454C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917122 | |||||||
| chr8:53917139 | T | TTTTTG | 33 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0063 others(30): Show |
33 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.511-22417_511-2241 others(9): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53917139 | ||||||
| chr8:53917182 | T | A | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.511-22394T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917182 | |||||||
| chr8:53917230 | G | C | 133 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(130): Show |
133 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.511-22346G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917230 | |||||||
| chr8:53917338 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.511-22238A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917338 | |||||||
| chr8:53917374 | C | A | 2 | a0001c0001t0002g0150 a0001c0001t0002g0172 |
2 | HG00140.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.511-22202C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917374 | |||||||
| chr8:53917440 | T | C | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-22136T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917440 | |||||||
| chr8:53917491 | A | T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-22085A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917491 | |||||||
| chr8:53917512 | T | C | 73 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(70): Show |
73 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.511-22064T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917512 | |||||||
| chr8:53917587 | T | C | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.511-21989T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917587 | |||||||
| chr8:53917719 | C | T | 133 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(130): Show |
133 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.511-21857C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917719 | |||||||
| chr8:53917720 | T | G | 59 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(56): Show |
59 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.511-21856T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917720 | |||||||
| chr8:53917756 | C | T | 73 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(70): Show |
73 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.511-21820C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917756 | |||||||
| chr8:53917805 | A | G | 133 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(130): Show |
133 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.511-21771A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917805 | |||||||
| chr8:53917851 | A | C | 42 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(39): Show |
42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-21725A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917851 | |||||||
| chr8:53917984 | A | G | 42 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(39): Show |
42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-21592A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917984 | |||||||
| chr8:53917996 | C | T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-21580C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53917996 | |||||||
| chr8:53918023 | A | G | 1 | a0001c0001t0003g0236 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.511-21553A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918023 | |||||||
| chr8:53918061 | G | C | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511-21515G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918061 | |||||||
| chr8:53918118 | T | C | 4 | a0001c0001t0002g0243 a0001c0003t0001g0028 a0001c0003t0003g0026 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-21458T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918118 | |||||||
| chr8:53918143 | T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-21433T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918143 | |||||||
| chr8:53918151 | G | A | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-21425G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918151 | |||||||
| chr8:53918248 | C | T | 2 | a0001c0002t0002g0004 a0001c0002t0002g0007 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.511-21328C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918248 | |||||||
| chr8:53918249 | C | G | 1 | a0001c0001t0002g0174 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.511-21327C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918249 | |||||||
| chr8:53918297 | T | C | 42 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(39): Show |
42 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.511-21279T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918297 | |||||||
| chr8:53918357 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.511-21219G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918357 | |||||||
| chr8:53918358 | T | A | 3 | a0001c0001t0001g0096 a0001c0001t0002g0174 a0001c0001t0002g0209 |
3 | NA18943.hp2 NA18961.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.511-21218T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918358 | |||||||
| chr8:53918375 | A | G | 27 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0049 others(24): Show |
27 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.511-21201A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918375 | |||||||
| chr8:53918380 | C | CT | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-21187dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53918380 | ||||||
| chr8:53918386 | T | TC | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-21190_511-2118 others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918386 | |||||||
| chr8:53918390 | C | CTTCCTT | 15 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(12): Show |
15 | HG01167.hp1 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.511-21184_511-2118 others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53918390 | ||||||
| chr8:53918394 | C | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-21182C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918394 | |||||||
| chr8:53918397 | C | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-21179C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918397 | |||||||
| chr8:53918398 | C | CTTTTTTT | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-21177_511-2117 others(11): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53918398 | ||||||
| chr8:53918398 | C | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-21178C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918398 | |||||||
| chr8:53918432 | G | A | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-21144G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918432 | |||||||
| chr8:53918481 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-21095C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918481 | |||||||
| chr8:53918482 | GGGTTCAA | G | 5 | a0001c0001t0001g0010 a0001c0001t0002g0246 a0001c0001t0004g0011 others(2): Show |
5 | HG02486.hp1 HG02970.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-21092_511-2108 others(11): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53918482 | ||||||
| chr8:53918615 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.511-20961T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918615 | |||||||
| chr8:53918678 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0003g0024 |
2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.511-20898G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918678 | |||||||
| chr8:53918774 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.511-20802G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918774 | |||||||
| chr8:53918789 | A | G | 52 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(49): Show |
52 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.511-20787A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53918789 | |||||||
| chr8:53919170 | T | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-20406T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919170 | |||||||
| chr8:53919288 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.511-20288C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919288 | |||||||
| chr8:53919315 | A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-20261A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919315 | |||||||
| chr8:53919346 | C | CT | 34 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0052 others(31): Show |
34 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.511-20215dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53919346 | ||||||
| chr8:53919346 | C | CTT | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-20216_511-2021 others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53919346 | ||||||
| chr8:53919496 | T | C | 132 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(129): Show |
132 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.511-20080T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919496 | |||||||
| chr8:53919557 | G | C | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-20019G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919557 | |||||||
| chr8:53919586 | T | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-19990T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919586 | |||||||
| chr8:53919596 | T | C | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-19980T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919596 | |||||||
| chr8:53919639 | A | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-19937A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919639 | |||||||
| chr8:53919772 | T | C | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-19804T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919772 | |||||||
| chr8:53919818 | G | A | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-19758G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53919818 | |||||||
| chr8:53920030 | T | A | 1 | a0001c0001t0001g0080 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.511-19546T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920030 | |||||||
| chr8:53920075 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.511-19501C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920075 | |||||||
| chr8:53920131 | T | C | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-19445T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920131 | |||||||
| chr8:53920243 | T | C | 4 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0004g0037 others(1): Show |
4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-19333T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920243 | |||||||
| chr8:53920320 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.511-19256C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920320 | |||||||
| chr8:53920322 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.511-19254C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920322 | |||||||
| chr8:53920446 | T | A | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-19130T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920446 | |||||||
| chr8:53920488 | A | G | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-19088A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920488 | |||||||
| chr8:53920589 | T | C | 1 | a0001c0001t0002g0168 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.511-18987T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920589 | |||||||
| chr8:53920779 | C | T | 3 | a0001c0001t0003g0022 a0001c0001t0005g0118 a0001c0001t0005g0119 |
3 | HG02055.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-18797C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53920779 | |||||||
| chr8:53921009 | C | T | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-18567C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921009 | |||||||
| chr8:53921011 | C | T | 73 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(70): Show |
73 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.511-18565C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921011 | |||||||
| chr8:53921070 | G | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0107 |
2 | NA18982.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.511-18506G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921070 | |||||||
| chr8:53921333 | C | A | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.511-18243C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921333 | |||||||
| chr8:53921405 | G | A | 4 | a0001c0001t0002g0246 a0001c0001t0004g0011 a0001c0001t0004g0012 others(1): Show |
4 | HG02486.hp1 HG03540.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-18171G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921405 | |||||||
| chr8:53921442 | CT | C | 8 | a0001c0001t0001g0031 a0001c0001t0001g0112 a0001c0001t0001g0147 others(5): Show |
8 | HG00323.hp1 HG00323.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.511-18117delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53921442 | ||||||
| chr8:53921477 | C | A | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-18099C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921477 | |||||||
| chr8:53921487 | C | A | 1 | a0001c0001t0002g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.511-18089C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921487 | |||||||
| chr8:53921632 | G | A | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511-17944G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921632 | |||||||
| chr8:53921757 | G | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-17819G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921757 | |||||||
| chr8:53921817 | T | A | 130 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(127): Show |
130 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.511-17759T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921817 | |||||||
| chr8:53921877 | T | C | 4 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0004g0037 others(1): Show |
4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-17699T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921877 | |||||||
| chr8:53921885 | A | AT | 73 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(70): Show |
73 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.511-17687dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53921885 | ||||||
| chr8:53921912 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0190 |
2 | HG00621.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.511-17664G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53921912 | |||||||
| chr8:53922087 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.511-17489T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922087 | |||||||
| chr8:53922132 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-17444C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922132 | |||||||
| chr8:53922302 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.511-17274T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922302 | |||||||
| chr8:53922325 | G | T | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-17251G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922325 | |||||||
| chr8:53922349 | A | G | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-17227A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922349 | |||||||
| chr8:53922372 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.511-17204C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922372 | |||||||
| chr8:53922416 | A | T | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-17160A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922416 | |||||||
| chr8:53922427 | A | G | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-17149A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922427 | |||||||
| chr8:53922926 | G | T | 10 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
10 | HG01496.hp2 HG02165.hp2 NA18948.hp2 others(7): Show |
intron_variant | MODIFIER | c.511-16650G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922926 | |||||||
| chr8:53922980 | G | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-16596G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53922980 | |||||||
| chr8:53923076 | G | A | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-16500G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923076 | |||||||
| chr8:53923137 | T | C | 5 | a0001c0001t0002g0131 a0001c0001t0002g0139 a0001c0001t0002g0184 others(2): Show |
5 | HG01243.hp1 HG01975.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-16439T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923137 | |||||||
| chr8:53923200 | G | T | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.511-16376G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923200 | |||||||
| chr8:53923212 | G | A | 37 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(34): Show |
37 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.511-16364G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923212 | |||||||
| chr8:53923381 | A | T | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(14): Show |
17 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.511-16195A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923381 | |||||||
| chr8:53923594 | C | CA | 7 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0082 others(4): Show |
7 | HG02027.hp1 NA18963.hp2 NA19055.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-15969dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53923594 | ||||||
| chr8:53923687 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.511-15889C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923687 | |||||||
| chr8:53923700 | A | G | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.511-15876A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923700 | |||||||
| chr8:53923708 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.511-15868A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923708 | |||||||
| chr8:53923726 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.511-15850C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53923726 | |||||||
| chr8:53924020 | C | A | 1 | a0001c0001t0002g0168 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.511-15556C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53924020 | |||||||
| chr8:53924345 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.511-15231G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53924345 | |||||||
| chr8:53924363 | T | C | 73 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(70): Show |
73 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.511-15213T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53924363 | |||||||
| chr8:53924486 | A | C | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-15090A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53924486 | |||||||
| chr8:53924642 | A | G | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-14934A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53924642 | |||||||
| chr8:53925436 | A | G | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-14140A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53925436 | |||||||
| chr8:53925756 | C | T | 2 | a0001c0001t0007g0033 a0001c0001t0007g0045 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.511-13820C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53925756 | |||||||
| chr8:53925779 | T | C | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-13797T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53925779 | |||||||
| chr8:53926034 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.511-13542C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926034 | |||||||
| chr8:53926135 | A | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0004g0037 others(1): Show |
4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-13441A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926135 | |||||||
| chr8:53926389 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0098 |
2 | NA18975.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.511-13187G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926389 | |||||||
| chr8:53926424 | A | G | 76 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(73): Show |
76 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.511-13152A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926424 | |||||||
| chr8:53926471 | AT | A | 15 | a0001c0001t0002g0020 a0001c0001t0002g0108 a0001c0001t0002g0117 others(12): Show |
15 | HG01192.hp2 HG02280.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.511-13097delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53926471 | ||||||
| chr8:53926530 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.511-13046C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926530 | |||||||
| chr8:53926686 | C | A | 1 | a0001c0001t0002g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.511-12890C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926686 | |||||||
| chr8:53926823 | G | C | 82 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(79): Show |
82 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.511-12753G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926823 | |||||||
| chr8:53926828 | G | A | 4 | a0001c0001t0002g0032 a0001c0001t0002g0038 a0001c0001t0004g0037 others(1): Show |
4 | HG01167.hp1 HG02809.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-12748G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926828 | |||||||
| chr8:53926868 | A | G | 134 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(131): Show |
134 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.511-12708A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926868 | |||||||
| chr8:53926908 | A | G | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0002g0106 others(1): Show |
4 | HG01243.hp2 HG02109.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-12668A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53926908 | |||||||
| chr8:53926916 | A | AAAAG | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-12645_511-1264 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53926916 | ||||||
| chr8:53927201 | G | GT | 31 | a0001c0001t0001g0010 a0001c0001t0001g0035 a0001c0001t0001g0040 others(28): Show |
31 | HG00597.hp1 HG00597.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.511-12358dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53927201 | ||||||
| chr8:53927201 | GT | G | 40 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0046 others(37): Show |
40 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.511-12358delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53927201 | ||||||
| chr8:53927201 | GTTTT | G | 33 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(30): Show |
33 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.511-12361_511-1235 others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53927201 | ||||||
| chr8:53927530 | C | T | 2 | a0001c0001t0007g0033 a0001c0001t0007g0045 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.511-12046C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53927530 | |||||||
| chr8:53928021 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.511-11555T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53928021 | |||||||
| chr8:53928246 | T | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(13): Show |
16 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.511-11330T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53928246 | |||||||
| chr8:53928613 | C | T | 4 | a0001c0001t0001g0112 a0001c0001t0001g0116 a0001c0001t0001g0197 others(1): Show |
4 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-10963C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53928613 | |||||||
| chr8:53928723 | T | C | 118 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(115): Show |
118 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.511-10853T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53928723 | |||||||
| chr8:53928916 | C | T | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-10660C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53928916 | |||||||
| chr8:53928979 | G | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-10597G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53928979 | |||||||
| chr8:53929065 | T | A | 76 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(73): Show |
76 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.511-10511T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929065 | |||||||
| chr8:53929382 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.511-10194A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929382 | |||||||
| chr8:53929407 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0130 others(3): Show |
6 | HG02132.hp1 HG02886.hp1 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-10169G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929407 | |||||||
| chr8:53929471 | A | G | 82 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(79): Show |
82 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.511-10105A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929471 | |||||||
| chr8:53929537 | G | A | 82 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(79): Show |
82 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.511-10039G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929537 | |||||||
| chr8:53929539 | A | G | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-10037A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929539 | |||||||
| chr8:53929607 | G | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(8): Show |
11 | HG01167.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.511-9969G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929607 | |||||||
| chr8:53929623 | G | A | 5 | a0001c0001t0002g0019 a0001c0001t0002g0083 a0001c0001t0002g0192 others(2): Show |
5 | NA18946.hp1 NA18952.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.511-9953G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929623 | |||||||
| chr8:53929726 | T | C | 6 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0001g0098 others(3): Show |
6 | HG00642.hp2 HG01358.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-9850T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53929726 | |||||||
| chr8:53930019 | A | G | 35 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(32): Show |
35 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.511-9557A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930019 | |||||||
| chr8:53930069 | T | A | 1 | a0001c0001t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.511-9507T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930069 | |||||||
| chr8:53930070 | T | A | 1 | a0001c0001t0002g0175 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.511-9506T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930070 | |||||||
| chr8:53930587 | C | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(13): Show |
16 | HG01069.hp2 HG01167.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.511-8989C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930587 | |||||||
| chr8:53930602 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.511-8974G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930602 | |||||||
| chr8:53930773 | T | C | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-8803T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930773 | |||||||
| chr8:53930795 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.511-8781T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53930795 | |||||||
| chr8:53931053 | C | G | 118 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(115): Show |
118 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.511-8523C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931053 | |||||||
| chr8:53931260 | T | C | 2 | a0001c0001t0002g0244 a0001c0001t0002g0245 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.511-8316T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931260 | |||||||
| chr8:53931321 | C | T | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-8255C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931321 | |||||||
| chr8:53931355 | G | A | 118 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(115): Show |
118 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.511-8221G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931355 | |||||||
| chr8:53931423 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.511-8153T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931423 | |||||||
| chr8:53931552 | A | AAAC | 24 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0047 others(21): Show |
24 | HG00323.hp2 HG00597.hp1 HG01993.hp1 others(21): Show |
intron_variant | MODIFIER | c.511-7985_511-7983d others(5): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | ||||||
| chr8:53931552 | A | AAACAAC | 13 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
13 | HG00438.hp2 HG00609.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.511-7988_511-7983d others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | ||||||
| chr8:53931552 | A | AAACAACA others(2): Show |
3 | a0001c0001t0001g0116 a0001c0001t0001g0197 a0001c0001t0001g0202 |
3 | HG01167.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.511-7991_511-7983d others(11): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | ||||||
| chr8:53931552 | AAACAAC | A | 24 | a0001c0001t0001g0042 a0001c0001t0001g0046 a0001c0001t0001g0049 others(21): Show |
24 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.511-7988_511-7983d others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | ||||||
| chr8:53931552 | AAACAACA others(2): Show |
A | 3 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0003t0002g0025 |
3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.511-7991_511-7983d others(11): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | ||||||
| chr8:53931552 | AAACAACA others(5): Show |
A | 55 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(52): Show |
55 | HG00741.hp1 HG01069.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.511-7994_511-7983d others(14): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | ||||||
| chr8:53931552 | AAACAACA others(8): Show |
A | 76 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(73): Show |
76 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.511-7997_511-7983d others(17): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53931552 | ||||||
| chr8:53931571 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.511-8005A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931571 | |||||||
| chr8:53931731 | T | C | 14 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0074 others(11): Show |
14 | HG01496.hp2 HG02027.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.511-7845T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931731 | |||||||
| chr8:53931733 | G | A | 4 | a0001c0001t0002g0243 a0001c0003t0001g0028 a0001c0003t0003g0026 others(1): Show |
4 | HG02280.hp2 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-7843G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931733 | |||||||
| chr8:53931973 | C | T | 75 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(72): Show |
75 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.511-7603C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53931973 | |||||||
| chr8:53932139 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(9): Show |
12 | HG01167.hp1 HG02055.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.511-7437G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932139 | |||||||
| chr8:53932227 | T | C | 1 | a0001c0001t0001g0231 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.511-7349T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932227 | |||||||
| chr8:53932271 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.511-7305G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932271 | |||||||
| chr8:53932365 | A | G | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-7211A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932365 | |||||||
| chr8:53932585 | T | C | 118 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(115): Show |
118 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.511-6991T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932585 | |||||||
| chr8:53932839 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.511-6737C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932839 | |||||||
| chr8:53932974 | G | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-6602G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53932974 | |||||||
| chr8:53933008 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0163 |
3 | NA18957.hp1 NA18961.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.511-6568C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933008 | |||||||
| chr8:53933052 | G | A | 1 | a0001c0001t0003g0169 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.511-6524G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933052 | |||||||
| chr8:53933057 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.511-6519A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933057 | |||||||
| chr8:53933070 | A | G | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.511-6506A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933070 | |||||||
| chr8:53933168 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.511-6408A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933168 | |||||||
| chr8:53933338 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.511-6238A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933338 | |||||||
| chr8:53933471 | A | G | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-6105A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933471 | |||||||
| chr8:53933481 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.511-6095G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933481 | |||||||
| chr8:53933653 | G | A | 74 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(71): Show |
74 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.511-5923G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933653 | |||||||
| chr8:53933708 | T | G | 1 | a0001c0001t0003g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.511-5868T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933708 | |||||||
| chr8:53933733 | C | T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-5843C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933733 | |||||||
| chr8:53933765 | G | A | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-5811G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933765 | |||||||
| chr8:53933805 | A | G | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-5771A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53933805 | |||||||
| chr8:53934048 | A | G | 82 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(79): Show |
82 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.511-5528A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934048 | |||||||
| chr8:53934162 | T | C | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.511-5414T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934162 | |||||||
| chr8:53934476 | A | G | 1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.511-5100A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934476 | |||||||
| chr8:53934477 | C | A | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-5099C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934477 | |||||||
| chr8:53934547 | C | G | 1 | a0001c0001t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.511-5029C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934547 | |||||||
| chr8:53934574 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.511-5002T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934574 | |||||||
| chr8:53934636 | C | T | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-4940C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934636 | |||||||
| chr8:53934661 | G | A | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-4915G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934661 | |||||||
| chr8:53934873 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.511-4703C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53934873 | |||||||
| chr8:53935000 | T | C | 134 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(131): Show |
134 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.511-4576T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935000 | |||||||
| chr8:53935075 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.511-4501A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935075 | |||||||
| chr8:53935099 | A | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-4477A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935099 | |||||||
| chr8:53935254 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.511-4322A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935254 | |||||||
| chr8:53935359 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.511-4217C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935359 | |||||||
| chr8:53935427 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511-4149C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935427 | |||||||
| chr8:53935521 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0002g0246 a0001c0001t0004g0011 others(2): Show |
5 | HG02486.hp1 HG02970.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-4055C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935521 | |||||||
| chr8:53935547 | T | C | 1 | a0001c0001t0002g0226 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.511-4029T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935547 | |||||||
| chr8:53935780 | C | G | 133 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(130): Show |
133 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.511-3796C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935780 | |||||||
| chr8:53935800 | G | C | 1 | a0001c0001t0002g0173 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.511-3776G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935800 | |||||||
| chr8:53935864 | A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-3712A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935864 | |||||||
| chr8:53935904 | T | C | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-3672T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935904 | |||||||
| chr8:53935932 | G | C | 1 | a0001c0001t0001g0125 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.511-3644G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53935932 | |||||||
| chr8:53936049 | C | A | 1 | a0001c0001t0002g0244 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.511-3527C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936049 | |||||||
| chr8:53936466 | G | C | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | HG02818.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.511-3110G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936466 | |||||||
| chr8:53936491 | G | C | 131 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(128): Show |
131 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.511-3085G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936491 | |||||||
| chr8:53936623 | T | A | 81 | a0001c0001t0001g0055 a0001c0001t0001g0060 a0001c0001t0001g0068 others(78): Show |
81 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.511-2953T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936623 | |||||||
| chr8:53936675 | C | A | 20 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0063 others(17): Show |
20 | HG01496.hp2 HG02027.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.511-2901C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936675 | |||||||
| chr8:53936699 | C | T | 2 | a0001c0001t0007g0033 a0001c0001t0007g0045 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.511-2877C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936699 | |||||||
| chr8:53936700 | G | A | 1 | a0001c0001t0009g0128 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.511-2876G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936700 | |||||||
| chr8:53936875 | T | C | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-2701T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53936875 | |||||||
| chr8:53937082 | A | C | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.511-2494A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937082 | |||||||
| chr8:53937119 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.511-2457C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937119 | |||||||
| chr8:53937128 | C | A | 6 | a0001c0001t0002g0021 a0001c0001t0002g0243 a0001c0001t0003g0030 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.511-2448C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937128 | |||||||
| chr8:53937406 | A | G | 36 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(33): Show |
36 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(33): Show |
intron_variant | MODIFIER | c.511-2170A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937406 | |||||||
| chr8:53937611 | A | T | 1 | a0001c0001t0003g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.511-1965A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937611 | |||||||
| chr8:53937617 | T | A | 1 | a0001c0003t0004g0027 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.511-1959T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937617 | |||||||
| chr8:53937677 | A | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02165.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.511-1899A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937677 | |||||||
| chr8:53937729 | A | G | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-1847A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937729 | |||||||
| chr8:53937773 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG01074.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.511-1803A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937773 | |||||||
| chr8:53937791 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-1785C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937791 | |||||||
| chr8:53937831 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.511-1745G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937831 | |||||||
| chr8:53937839 | G | A | 2 | a0001c0001t0007g0033 a0001c0001t0007g0045 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.511-1737G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53937839 | |||||||
| chr8:53938053 | G | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0098 |
2 | NA18975.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.511-1523G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53938053 | |||||||
| chr8:53938249 | C | T | 133 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(130): Show |
133 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.511-1327C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53938249 | |||||||
| chr8:53938312 | T | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.511-1264T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53938312 | |||||||
| chr8:53938712 | A | G | 34 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(31): Show |
34 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.511-864A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53938712 | |||||||
| chr8:53938906 | G | A | 1 | a0001c0001t0002g0150 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.511-670G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53938906 | |||||||
| chr8:53939242 | G | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(11): Show |
14 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.511-334G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53939242 | |||||||
| chr8:53939256 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.511-320T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53939256 | |||||||
| chr8:53939259 | GTAGCACT others(3): Show |
G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0197 a0001c0001t0001g0202 |
3 | HG01167.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.511-315_511-306del others(10): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr8 | 53939259 | ||||||
| chr8:53939270 | T | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0197 a0001c0001t0001g0202 |
3 | HG01167.hp2 HG01169.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.511-306T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53939270 | |||||||
| chr8:53939282 | A | G | 2 | a0001c0001t0002g0053 a0001c0001t0002g0070 |
2 | NA18943.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.511-294A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53939282 | |||||||
| chr8:53939332 | G | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0143 others(11): Show |
14 | HG01069.hp2 HG01167.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.511-244G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 2/5 | chr8 | 53939332 | |||||||
| chr8:53939891 | A | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0143 a0001c0001t0002g0246 others(3): Show |
6 | HG02486.hp1 HG02622.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.659+167A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53939891 | |||||||
| chr8:53940039 | C | T | 48 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(45): Show |
48 | HG00741.hp1 HG01109.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.659+315C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940039 | |||||||
| chr8:53940083 | C | G | 110 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(107): Show |
110 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.659+359C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940083 | |||||||
| chr8:53940098 | G | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.659+374G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940098 | |||||||
| chr8:53940227 | T | C | 163 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(160): Show |
163 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.659+503T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940227 | |||||||
| chr8:53940542 | G | C | 35 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(32): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.659+818G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940542 | |||||||
| chr8:53940546 | A | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.659+822A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940546 | |||||||
| chr8:53940577 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG01074.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.659+853G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940577 | |||||||
| chr8:53940876 | C | T | 2 | a0001c0001t0002g0218 a0001c0001t0002g0223 |
2 | HG01070.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.659+1152C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53940876 | |||||||
| chr8:53941145 | T | G | 164 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(161): Show |
164 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.659+1421T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53941145 | |||||||
| chr8:53941994 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.659+2270C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53941994 | |||||||
| chr8:53942214 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.659+2490G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53942214 | |||||||
| chr8:53942361 | G | A | 38 | a0001c0001t0001g0023 a0001c0001t0001g0052 a0001c0001t0001g0054 others(35): Show |
38 | HG00741.hp1 HG01167.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.659+2637G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53942361 | |||||||
| chr8:53942567 | T | A | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.659+2843T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53942567 | |||||||
| chr8:53942602 | T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.659+2878T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53942602 | |||||||
| chr8:53942617 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.659+2893G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53942617 | |||||||
| chr8:53942826 | TA | T | 193 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(190): Show |
193 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.659+3121delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53942826 | ||||||
| chr8:53942826 | TAA | T | 5 | a0001c0001t0001g0088 a0001c0001t0003g0051 a0001c0001t0005g0119 others(2): Show |
5 | HG01069.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.659+3120_659+3121d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53942826 | ||||||
| chr8:53943025 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.659+3301A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943025 | |||||||
| chr8:53943120 | T | C | 111 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(108): Show |
111 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.659+3396T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943120 | |||||||
| chr8:53943202 | C | A | 1 | a0001c0001t0002g0122 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.660-3463C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943202 | |||||||
| chr8:53943267 | A | G | 12 | a0001c0001t0001g0054 a0001c0001t0001g0075 a0001c0001t0001g0076 others(9): Show |
12 | HG02027.hp2 HG02165.hp2 HG04184.hp1 others(9): Show |
intron_variant | MODIFIER | c.660-3398A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943267 | |||||||
| chr8:53943312 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.660-3353C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943312 | |||||||
| chr8:53943615 | C | A | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.660-3050C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943615 | |||||||
| chr8:53943741 | A | AT | 150 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(147): Show |
150 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.660-2924_660-2923i others(3): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53943741 | |||||||
| chr8:53943996 | T | TAC | 9 | a0001c0001t0001g0100 a0001c0001t0001g0163 a0001c0001t0001g0231 others(6): Show |
9 | HG02040.hp1 HG02055.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.660-2642_660-2641d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53943996 | ||||||
| chr8:53943996 | TAC | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0069 a0001c0001t0001g0092 others(5): Show |
8 | HG02809.hp2 HG02886.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.660-2642_660-2641d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53943996 | ||||||
| chr8:53943996 | TACACAC | T | 26 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0075 others(23): Show |
26 | HG00741.hp1 HG01109.hp2 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.660-2646_660-2641d others(8): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53943996 | ||||||
| chr8:53944078 | T | TAAAG | 143 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0035 others(140): Show |
143 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.660-2586_660-2585i others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53944078 | ||||||
| chr8:53944136 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.660-2529A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944136 | |||||||
| chr8:53944322 | A | G | 98 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.660-2343A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944322 | |||||||
| chr8:53944345 | A | G | 1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.660-2320A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944345 | |||||||
| chr8:53944410 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.660-2255C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944410 | |||||||
| chr8:53944450 | A | C | 1 | a0001c0001t0002g0232 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.660-2215A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944450 | |||||||
| chr8:53944453 | A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.660-2212A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944453 | |||||||
| chr8:53944460 | C | T | 3 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0003t0002g0025 |
3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.660-2205C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944460 | |||||||
| chr8:53944535 | C | T | 176 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0031 others(173): Show |
176 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.660-2130C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944535 | |||||||
| chr8:53944537 | C | CA | 76 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0041 others(73): Show |
76 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.660-2113dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53944537 | ||||||
| chr8:53944537 | CA | C | 14 | a0001c0001t0001g0023 a0001c0001t0002g0111 a0001c0001t0002g0161 others(11): Show |
14 | HG00323.hp1 HG01257.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.660-2113delA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53944537 | ||||||
| chr8:53944561 | G | C | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.660-2104G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944561 | |||||||
| chr8:53944641 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.660-2024C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944641 | |||||||
| chr8:53944672 | T | C | 2 | a0001c0001t0002g0021 a0001c0001t0011g0208 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.660-1993T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944672 | |||||||
| chr8:53944748 | G | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.660-1917G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944748 | |||||||
| chr8:53944807 | C | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.660-1858C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53944807 | |||||||
| chr8:53945028 | C | T | 7 | a0001c0001t0002g0021 a0001c0001t0002g0144 a0001c0001t0005g0118 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.660-1637C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945028 | |||||||
| chr8:53945140 | G | A | 71 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(68): Show |
71 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.660-1525G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945140 | |||||||
| chr8:53945381 | C | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.660-1284C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945381 | |||||||
| chr8:53945482 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.660-1183T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945482 | |||||||
| chr8:53945809 | A | T | 1 | a0001c0001t0001g0255 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.660-856A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945809 | |||||||
| chr8:53945844 | G | A | 3 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0008g0039 |
3 | HG01069.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.660-821G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945844 | |||||||
| chr8:53945887 | C | CA | 42 | a0001c0001t0001g0081 a0001c0001t0001g0090 a0001c0001t0001g0093 others(39): Show |
42 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.660-765dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr8 | 53945887 | ||||||
| chr8:53945934 | G | A | 140 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(137): Show |
140 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.660-731G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53945934 | |||||||
| chr8:53946107 | A | G | 2 | a0001c0001t0002g0117 a0001c0001t0002g0210 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.660-558A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53946107 | |||||||
| chr8:53946162 | T | A | 2 | a0001c0001t0002g0021 a0001c0001t0011g0208 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.660-503T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53946162 | |||||||
| chr8:53946229 | T | A | 1 | a0001c0001t0001g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.660-436T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53946229 | |||||||
| chr8:53946421 | T | A | 47 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(44): Show |
47 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.660-244T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53946421 | |||||||
| chr8:53946469 | T | C | 143 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(140): Show |
143 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.660-196T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 3/5 | chr8 | 53946469 | |||||||
| chr8:53946947 | A | G | 1 | a0001c0002t0001g0005 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.743+199A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53946947 | |||||||
| chr8:53947034 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.743+286T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947034 | |||||||
| chr8:53947058 | A | G | 3 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0003t0002g0025 |
3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+310A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947058 | |||||||
| chr8:53947135 | T | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+387T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947135 | |||||||
| chr8:53947167 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.743+419C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947167 | |||||||
| chr8:53947168 | T | G | 216 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(213): Show |
216 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.743+420T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947168 | |||||||
| chr8:53947193 | A | T | 8 | a0001c0001t0001g0115 a0001c0001t0002g0053 a0001c0001t0002g0070 others(5): Show |
8 | HG01099.hp1 HG01496.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+445A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947193 | |||||||
| chr8:53947194 | C | T | 8 | a0001c0001t0001g0115 a0001c0001t0002g0053 a0001c0001t0002g0070 others(5): Show |
8 | HG01099.hp1 HG01496.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+446C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947194 | |||||||
| chr8:53947196 | C | CGCTATAT others(51): Show |
2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+473_743+474ins others(58): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947196 | ||||||
| chr8:53947196 | C | CGCTATAT others(88): Show |
1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+473_743+474ins others(95): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947196 | ||||||
| chr8:53947196 | C | T | 1 | a0001c0001t0003g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.743+448C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947196 | |||||||
| chr8:53947196 | CGCTATAT others(26): Show |
C | 1 | a0001c0001t0001g0254 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.743+503_743+535del others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947196 | ||||||
| chr8:53947207 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.743+459A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947207 | |||||||
| chr8:53947216 | A | G | 15 | a0001c0001t0002g0020 a0001c0001t0002g0038 a0001c0001t0002g0108 others(12): Show |
15 | HG01192.hp2 HG01891.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.743+468A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947216 | |||||||
| chr8:53947247 | ATATT | A | 3 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0001t0011g0208 |
3 | HG02055.hp1 HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+507_743+510del others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947247 | ||||||
| chr8:53947251 | T | A | 8 | a0001c0001t0001g0115 a0001c0001t0002g0053 a0001c0001t0002g0070 others(5): Show |
8 | HG01099.hp1 HG01496.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+503T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947251 | |||||||
| chr8:53947284 | A | T | 5 | a0001c0001t0002g0235 a0001c0001t0006g0043 a0001c0001t0006g0044 others(2): Show |
5 | HG01069.hp2 HG01109.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.743+536A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947284 | |||||||
| chr8:53947300 | T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+552T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947300 | |||||||
| chr8:53947307 | TATAGTAT others(25): Show |
T | 2 | a0001c0001t0001g0069 a0001c0001t0002g0207 |
2 | HG00438.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.743+595_743+626del others(32): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947307 | ||||||
| chr8:53947308 | A | G | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+560A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947308 | |||||||
| chr8:53947312 | T | C | 16 | a0001c0001t0001g0023 a0001c0001t0002g0235 a0001c0001t0003g0001 others(13): Show |
16 | HG01109.hp2 HG01891.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.743+564T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947312 | |||||||
| chr8:53947319 | A | AT | 3 | a0001c0001t0002g0235 a0001c0003t0002g0025 a0001c0003t0002g0029 |
3 | HG01109.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743+573dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947319 | ||||||
| chr8:53947325 | T | C | 5 | a0001c0001t0002g0235 a0001c0001t0005g0118 a0001c0001t0005g0119 others(2): Show |
5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+577T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947325 | |||||||
| chr8:53947336 | T | A | 5 | a0001c0001t0002g0235 a0001c0001t0005g0118 a0001c0001t0005g0119 others(2): Show |
5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+588T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947336 | |||||||
| chr8:53947337 | A | G | 5 | a0001c0001t0002g0235 a0001c0001t0005g0118 a0001c0001t0005g0119 others(2): Show |
5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+589A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947337 | |||||||
| chr8:53947339 | G | T | 5 | a0001c0001t0002g0235 a0001c0001t0005g0118 a0001c0001t0005g0119 others(2): Show |
5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+591G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947339 | |||||||
| chr8:53947343 | G | T | 1 | a0001c0001t0001g0049 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.743+595G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947343 | |||||||
| chr8:53947344 | T | A | 1 | a0001c0001t0001g0049 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.743+596T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947344 | |||||||
| chr8:53947344 | T | C | 1 | a0001c0003t0002g0029 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.743+596T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947344 | |||||||
| chr8:53947345 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.743+597A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947345 | |||||||
| chr8:53947351 | ATT | A | 4 | a0001c0001t0003g0030 a0001c0001t0003g0102 a0001c0001t0003g0103 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+604_743+605del others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947351 | |||||||
| chr8:53947361 | CTA | C | 4 | a0001c0001t0002g0235 a0001c0001t0005g0118 a0001c0001t0005g0119 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+620_743+621del others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947361 | ||||||
| chr8:53947375 | T | G | 5 | a0001c0001t0002g0235 a0001c0001t0005g0118 a0001c0001t0005g0119 others(2): Show |
5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+627T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947375 | |||||||
| chr8:53947376 | A | T | 5 | a0001c0001t0002g0235 a0001c0001t0005g0118 a0001c0001t0005g0119 others(2): Show |
5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+628A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947376 | |||||||
| chr8:53947377 | G | A | 5 | a0001c0001t0002g0235 a0001c0001t0005g0118 a0001c0001t0005g0119 others(2): Show |
5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+629G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947377 | |||||||
| chr8:53947380 | T | C | 36 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0120 others(33): Show |
36 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.743+632T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947380 | |||||||
| chr8:53947382 | T | TA | 5 | a0001c0001t0002g0235 a0001c0001t0005g0118 a0001c0001t0005g0119 others(2): Show |
5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+634_743+635ins others(1): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947382 | |||||||
| chr8:53947383 | TTA | T | 36 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0120 others(33): Show |
36 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.743+641_743+642del others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947383 | ||||||
| chr8:53947408 | G | GTATA | 141 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(138): Show |
141 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.743+662_743+663ins others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947408 | ||||||
| chr8:53947411 | C | T | 5 | a0001c0001t0002g0235 a0001c0001t0005g0118 a0001c0001t0005g0119 others(2): Show |
5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+663C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947411 | |||||||
| chr8:53947430 | T | TAA | 5 | a0001c0001t0002g0235 a0001c0001t0005g0118 a0001c0001t0005g0119 others(2): Show |
5 | HG01109.hp2 HG02055.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.743+682_743+683ins others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947430 | |||||||
| chr8:53947440 | T | C | 4 | a0001c0001t0002g0106 a0001c0001t0002g0232 a0001c0001t0007g0033 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+692T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947440 | |||||||
| chr8:53947463 | TAA | T | 3 | a0001c0001t0002g0235 a0001c0003t0002g0025 a0001c0003t0002g0029 |
3 | HG01109.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743+716_743+717del others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947463 | |||||||
| chr8:53947465 | AGATATAG others(26): Show |
A | 1 | a0001c0001t0001g0066 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.743+816_743+848del others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947465 | ||||||
| chr8:53947491 | C | CTA | 3 | a0001c0001t0002g0235 a0001c0003t0002g0025 a0001c0003t0002g0029 |
3 | HG01109.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743+748_743+749dup others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947491 | ||||||
| chr8:53947498 | G | A | 3 | a0001c0001t0002g0235 a0001c0003t0002g0025 a0001c0003t0002g0029 |
3 | HG01109.hp2 HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743+750G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947498 | |||||||
| chr8:53947498 | G | T | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+750G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947498 | |||||||
| chr8:53947519 | A | G | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+771A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947519 | |||||||
| chr8:53947531 | G | A | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+783G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947531 | |||||||
| chr8:53947541 | TATACATT others(61): Show |
T | 4 | a0001c0001t0003g0022 a0001c0001t0006g0043 a0001c0001t0006g0044 others(1): Show |
4 | HG01069.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+816_743+883del others(68): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947541 | ||||||
| chr8:53947557 | C | CTA | 53 | a0001c0001t0001g0018 a0001c0001t0001g0041 a0001c0001t0001g0042 others(50): Show |
53 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.743+814_743+815dup others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947557 | ||||||
| chr8:53947557 | CTATATAG others(28): Show |
C | 7 | a0001c0001t0001g0193 a0001c0001t0004g0011 a0001c0001t0004g0012 others(4): Show |
7 | HG00609.hp1 HG01167.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.743+826_743+860del others(35): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947557 | ||||||
| chr8:53947574 | T | C | 13 | a0001c0001t0001g0054 a0001c0001t0001g0072 a0001c0001t0001g0077 others(10): Show |
13 | HG00140.hp2 HG00741.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.743+826T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947574 | |||||||
| chr8:53947574 | T | TATACATT others(28): Show |
1 | a0001c0001t0002g0214 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.743+1001_743+1035d others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947574 | ||||||
| chr8:53947574 | TATACATT others(28): Show |
T | 17 | a0001c0001t0001g0023 a0001c0001t0002g0021 a0001c0001t0003g0001 others(14): Show |
17 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.743+1001_743+1035d others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947574 | ||||||
| chr8:53947579 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.743+831A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947579 | |||||||
| chr8:53947590 | CTA | C | 37 | a0001c0001t0001g0014 a0001c0001t0001g0120 a0001c0001t0001g0163 others(34): Show |
37 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.743+849_743+850del others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947590 | ||||||
| chr8:53947592 | A | ATATAGGA others(24): Show |
1 | a0001c0001t0002g0178 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.743+848_743+849ins others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947592 | ||||||
| chr8:53947609 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0005g0118 a0001c0001t0005g0119 others(2): Show |
5 | HG02055.hp1 HG02886.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.743+861C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947609 | |||||||
| chr8:53947679 | CATACATT others(133): Show |
C | 2 | a0001c0001t0003g0102 a0001c0001t0003g0103 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.743+966_743+1105de others(1): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947679 | ||||||
| chr8:53947695 | C | T | 21 | a0001c0001t0002g0016 a0001c0001t0002g0038 a0001c0001t0002g0108 others(18): Show |
21 | HG01192.hp2 HG01891.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.743+947C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947695 | |||||||
| chr8:53947714 | C | T | 130 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(127): Show |
130 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.743+966C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947714 | |||||||
| chr8:53947730 | C | T | 1 | a0001c0001t0002g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.743+982C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947730 | |||||||
| chr8:53947749 | C | T | 145 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(142): Show |
145 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.743+1001C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947749 | |||||||
| chr8:53947749 | CATACATT others(28): Show |
C | 2 | a0001c0001t0002g0122 a0001c0001t0002g0150 |
2 | HG00140.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.743+1096_743+1130d others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947749 | ||||||
| chr8:53947784 | T | C | 35 | a0001c0001t0001g0093 a0001c0001t0001g0105 a0001c0001t0001g0120 others(32): Show |
35 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.743+1036T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947784 | |||||||
| chr8:53947809 | G | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0085 others(4): Show |
7 | HG02027.hp2 HG02083.hp1 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.743+1061G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947809 | |||||||
| chr8:53947813 | A | ATAGTATA others(28): Show |
1 | a0001c0001t0001g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.743+1095_743+1096i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947813 | ||||||
| chr8:53947813 | A | G | 8 | a0001c0001t0001g0054 a0001c0001t0001g0077 a0001c0001t0001g0085 others(5): Show |
8 | HG02027.hp2 HG02083.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+1065A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947813 | |||||||
| chr8:53947823 | C | T | 3 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0003t0002g0025 |
3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1075C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947823 | |||||||
| chr8:53947844 | G | A | 134 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(131): Show |
134 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.743+1096G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947844 | |||||||
| chr8:53947848 | A | ATAGTATA others(28): Show |
6 | a0001c0001t0001g0063 a0001c0001t0001g0086 a0001c0001t0001g0096 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.743+1110_743+1144d others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53947848 | ||||||
| chr8:53947848 | A | G | 134 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(131): Show |
134 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.743+1100A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947848 | |||||||
| chr8:53947858 | C | T | 3 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0003t0002g0025 |
3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1110C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947858 | |||||||
| chr8:53947874 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.743+1126A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947874 | |||||||
| chr8:53947890 | A | C | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.743+1142A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947890 | |||||||
| chr8:53947911 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0073 |
2 | HG03669.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.743+1163T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947911 | |||||||
| chr8:53947913 | G | T | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1165G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53947913 | |||||||
| chr8:53948070 | T | TTATATAT others(20): Show |
3 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0008g0039 |
3 | HG01069.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.743+1367_743+1393d others(29): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948070 | ||||||
| chr8:53948124 | A | ATATATAT others(28): Show |
2 | a0001c0001t0003g0022 a0001c0001t0003g0051 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.743+1414_743+1448d others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948124 | ||||||
| chr8:53948124 | ATATATAT others(28): Show |
A | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.743+1414_743+1448d others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948124 | ||||||
| chr8:53948133 | CTA | C | 3 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 |
3 | HG03540.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.743+1393_743+1394d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948133 | ||||||
| chr8:53948135 | A | ATATATAT others(28): Show |
2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1421_743+1422i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948135 | ||||||
| chr8:53948210 | TAA | T | 47 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(44): Show |
47 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.743+1463_743+1464d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948210 | |||||||
| chr8:53948211 | A | G | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1463A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948211 | |||||||
| chr8:53948213 | G | T | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1465G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948213 | |||||||
| chr8:53948250 | GTATA | G | 3 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0008g0039 |
3 | HG01069.hp2 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.743+1507_743+1510d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948250 | ||||||
| chr8:53948295 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.743+1547G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948295 | |||||||
| chr8:53948318 | ATATG | A | 3 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0003t0002g0025 |
3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1571_743+1574d others(6): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948318 | |||||||
| chr8:53948330 | TAA | T | 12 | a0001c0001t0002g0106 a0001c0001t0002g0232 a0001c0001t0004g0011 others(9): Show |
12 | HG01070.hp2 HG01071.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+1583_743+1584d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948330 | |||||||
| chr8:53948341 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.743+1593A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948341 | |||||||
| chr8:53948364 | GAC | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0041 a0001c0001t0001g0068 |
3 | HG00438.hp2 HG03453.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.743+1620_743+1621d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948364 | ||||||
| chr8:53948366 | C | T | 3 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0003t0002g0025 |
3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1618C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948366 | |||||||
| chr8:53948381 | T | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0252 a0001c0001t0002g0108 others(3): Show |
6 | HG00438.hp1 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.743+1633T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948381 | |||||||
| chr8:53948399 | T | C | 142 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(139): Show |
142 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.743+1651T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948399 | |||||||
| chr8:53948404 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743+1656T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948404 | |||||||
| chr8:53948412 | T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1664T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948412 | |||||||
| chr8:53948414 | C | T | 58 | a0001c0001t0001g0014 a0001c0001t0001g0093 a0001c0001t0001g0105 others(55): Show |
58 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.743+1666C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948414 | |||||||
| chr8:53948429 | AGATACAG others(24): Show |
A | 1 | a0001c0001t0002g0201 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.743+1784_743+1814d others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948429 | ||||||
| chr8:53948437 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743+1689T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948437 | |||||||
| chr8:53948445 | T | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1697T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948445 | |||||||
| chr8:53948447 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1699C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948447 | |||||||
| chr8:53948460 | T | A | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1712T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948460 | |||||||
| chr8:53948460 | T | TAA | 5 | a0001c0001t0002g0106 a0001c0001t0002g0232 a0001c0001t0005g0119 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.743+1712_743+1713i others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948460 | |||||||
| chr8:53948532 | T | C | 1 | a0001c0001t0002g0192 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.743+1784T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948532 | |||||||
| chr8:53948532 | T | TATATTTA others(24): Show |
1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.743+1868_743+1898d others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948532 | ||||||
| chr8:53948532 | TATATTTA others(24): Show |
T | 7 | a0001c0001t0001g0163 a0001c0001t0002g0117 a0001c0001t0002g0157 others(4): Show |
7 | HG01358.hp2 HG02280.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.743+1868_743+1898d others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948532 | ||||||
| chr8:53948553 | T | TGATACAG others(57): Show |
1 | a0001c0001t0002g0247 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.743+1814_743+1815i others(66): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948553 | ||||||
| chr8:53948563 | C | T | 201 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(198): Show |
201 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.743+1815C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948563 | |||||||
| chr8:53948584 | T | A | 2 | a0001c0001t0002g0247 a0001c0001t0003g0030 |
2 | HG02273.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.743+1836T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948584 | |||||||
| chr8:53948584 | T | TAA | 3 | a0001c0001t0002g0156 a0001c0001t0002g0243 a0001c0003t0002g0025 |
3 | HG01346.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.743+1836_743+1837i others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948584 | |||||||
| chr8:53948594 | C | T | 189 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0023 others(186): Show |
189 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.743+1846C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948594 | |||||||
| chr8:53948602 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1854C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948602 | |||||||
| chr8:53948610 | ATATATGA others(55): Show |
A | 3 | a0001c0001t0001g0048 a0001c0001t0003g0030 a0001c0001t0004g0037 |
3 | HG01167.hp1 HG02630.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.743+1868_743+1929d others(64): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948610 | ||||||
| chr8:53948615 | T | A | 8 | a0001c0001t0002g0156 a0001c0001t0002g0243 a0001c0001t0002g0247 others(5): Show |
8 | HG01168.hp2 HG01169.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.743+1867T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948615 | |||||||
| chr8:53948615 | T | TAA | 23 | a0001c0001t0001g0093 a0001c0001t0001g0120 a0001c0001t0001g0229 others(20): Show |
23 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.743+1867_743+1868i others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948615 | |||||||
| chr8:53948615 | TGATACAG others(88): Show |
T | 1 | a0001c0001t0005g0119 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.743+1898_743+1992d others(97): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948615 | ||||||
| chr8:53948625 | C | T | 49 | a0001c0001t0001g0069 a0001c0001t0001g0093 a0001c0001t0001g0105 others(46): Show |
49 | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.743+1877C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948625 | |||||||
| chr8:53948633 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1885C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948633 | |||||||
| chr8:53948639 | CTA | C | 24 | a0001c0001t0001g0093 a0001c0001t0001g0120 a0001c0001t0001g0229 others(21): Show |
24 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.743+1898_743+1899d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948639 | ||||||
| chr8:53948641 | A | ATATAAGA others(22): Show |
1 | a0001c0001t0002g0247 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.743+1897_743+1898i others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | ||||||
| chr8:53948641 | A | ATATATGA others(86): Show |
1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.743+1898_743+1899i others(95): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | ||||||
| chr8:53948641 | A | ATATATGA others(84): Show |
1 | a0001c0001t0011g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.743+1898_743+1899i others(93): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | ||||||
| chr8:53948641 | ATATATAA others(24): Show |
A | 20 | a0001c0001t0001g0061 a0001c0001t0001g0086 a0001c0001t0001g0115 others(17): Show |
20 | HG01070.hp1 HG01099.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.743+2220_743+2250d others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | ||||||
| chr8:53948641 | ATATATAA others(55): Show |
A | 26 | a0001c0001t0001g0015 a0001c0001t0001g0068 a0001c0001t0001g0077 others(23): Show |
26 | HG00323.hp1 HG00609.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.743+2189_743+2250d others(64): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | ||||||
| chr8:53948641 | ATATATAA others(86): Show |
A | 54 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0041 others(51): Show |
54 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.743+2158_743+2250d others(95): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | ||||||
| chr8:53948641 | ATATATAA others(117): Show |
A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0090 a0001c0001t0002g0132 others(1): Show |
4 | HG02818.hp1 HG02896.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+2127_743+2250d others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | ||||||
| chr8:53948641 | ATATATAA others(148): Show |
A | 4 | a0001c0001t0001g0049 a0001c0001t0002g0244 a0001c0001t0002g0245 others(1): Show |
4 | HG00609.hp2 HG02486.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+2096_743+2250d others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948641 | ||||||
| chr8:53948646 | TAA | T | 26 | a0001c0001t0001g0069 a0001c0001t0001g0123 a0001c0001t0002g0016 others(23): Show |
26 | HG00408.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.743+1899_743+1900d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948646 | |||||||
| chr8:53948648 | A | T | 1 | a0001c0001t0011g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.743+1900A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948648 | |||||||
| chr8:53948658 | C | T | 6 | a0001c0001t0001g0105 a0001c0001t0001g0163 a0001c0001t0002g0133 others(3): Show |
6 | HG00408.hp1 HG02055.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.743+1910C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948658 | |||||||
| chr8:53948666 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1918C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948666 | |||||||
| chr8:53948672 | C | CTA | 3 | a0001c0001t0002g0164 a0001c0001t0002g0201 a0001c0001t0011g0208 |
3 | HG00408.hp1 HG02109.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.743+1929_743+1930d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948672 | ||||||
| chr8:53948674 | ATATAAGA others(22): Show |
A | 6 | a0001c0001t0001g0069 a0001c0001t0001g0123 a0001c0001t0002g0106 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.743+1931_743+1959d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948674 | ||||||
| chr8:53948674 | ATATAAGA others(53): Show |
A | 3 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 |
3 | HG03540.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.743+1931_743+1990d others(62): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948674 | ||||||
| chr8:53948674 | ATATAAGA others(115): Show |
A | 12 | a0001c0001t0002g0020 a0001c0001t0002g0038 a0001c0001t0002g0168 others(9): Show |
12 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+1931_743+2052d others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948674 | ||||||
| chr8:53948674 | ATATAAGA others(146): Show |
A | 1 | a0001c0001t0002g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.743+1931_743+2083d others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948674 | ||||||
| chr8:53948679 | A | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0179 a0001c0002t0002g0009 |
3 | HG02895.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.743+1931A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948679 | |||||||
| chr8:53948689 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+1941C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948689 | |||||||
| chr8:53948705 | ATATAAGA others(84): Show |
A | 1 | a0001c0002t0002g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.743+1962_743+2052d others(93): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948705 | ||||||
| chr8:53948705 | ATATAAGA others(115): Show |
A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0179 |
2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.743+1962_743+2083d others(2): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948705 | ||||||
| chr8:53948720 | C | T | 2 | a0001c0001t0005g0119 a0001c0003t0002g0025 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+1972C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948720 | |||||||
| chr8:53948751 | C | T | 2 | a0001c0001t0005g0119 a0001c0003t0002g0025 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.743+2003C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948751 | |||||||
| chr8:53948782 | C | T | 1 | a0001c0001t0005g0119 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.743+2034C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948782 | |||||||
| chr8:53948790 | C | T | 45 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0035 others(42): Show |
45 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.743+2042C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948790 | |||||||
| chr8:53948813 | C | T | 34 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(31): Show |
34 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.743+2065C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948813 | |||||||
| chr8:53948821 | C | T | 64 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0031 others(61): Show |
64 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.743+2073C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948821 | |||||||
| chr8:53948844 | C | T | 78 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0031 others(75): Show |
78 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.743+2096C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948844 | |||||||
| chr8:53948852 | C | T | 86 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0031 others(83): Show |
86 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.743+2104C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948852 | |||||||
| chr8:53948875 | C | T | 149 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(146): Show |
149 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.743+2127C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948875 | |||||||
| chr8:53948883 | C | CATATGCT others(24): Show |
1 | a0001c0001t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.743+2157_743+2158i others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948883 | ||||||
| chr8:53948883 | C | CTATATAA others(18): Show |
1 | a0001c0001t0002g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.743+2135_743+2136i others(27): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948883 | |||||||
| chr8:53948883 | C | T | 156 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(153): Show |
156 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.743+2135C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948883 | |||||||
| chr8:53948906 | C | T | 179 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(176): Show |
179 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.743+2158C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948906 | |||||||
| chr8:53948914 | C | CATATGCT others(55): Show |
1 | a0001c0001t0002g0178 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.743+2188_743+2189i others(64): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948914 | ||||||
| chr8:53948914 | C | T | 200 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(197): Show |
200 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.743+2166C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948914 | |||||||
| chr8:53948937 | C | T | 209 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(206): Show |
209 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.743+2189C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948937 | |||||||
| chr8:53948945 | C | T | 209 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(206): Show |
209 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.743+2197C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948945 | |||||||
| chr8:53948968 | C | CATATTTA others(24): Show |
1 | a0001c0001t0011g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.743+2228_743+2258d others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948968 | ||||||
| chr8:53948968 | C | T | 244 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(241): Show |
244 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.743+2220C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948968 | |||||||
| chr8:53948976 | C | CATATGCT others(24): Show |
1 | a0001c0001t0002g0073 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.743+2450_743+2480d others(33): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948976 | ||||||
| chr8:53948976 | C | T | 234 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
234 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.743+2228C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948976 | |||||||
| chr8:53948976 | CATATGCT others(55): Show |
C | 1 | a0001c0001t0002g0104 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.743+2419_743+2480d others(64): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948976 | ||||||
| chr8:53948984 | ATATAAGA others(22): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.743+2241_743+2269d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53948984 | ||||||
| chr8:53948999 | T | C | 2 | a0001c0001t0002g0217 a0001c0001t0002g0251 |
2 | HG01099.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.743+2251T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53948999 | |||||||
| chr8:53949007 | T | C | 4 | a0001c0001t0002g0217 a0001c0001t0002g0251 a0001c0001t0005g0118 others(1): Show |
4 | HG01099.hp2 HG01243.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.743+2259T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949007 | |||||||
| chr8:53949012 | G | A | 4 | a0001c0001t0002g0094 a0001c0001t0002g0134 a0001c0001t0002g0178 others(1): Show |
4 | HG00597.hp2 HG02280.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+2264G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949012 | |||||||
| chr8:53949013 | C | CTATATAT others(28): Show |
2 | a0001c0001t0002g0134 a0001c0001t0002g0178 |
2 | HG03942.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.743+2271_743+2272i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949013 | ||||||
| chr8:53949015 | ATATAAGA others(22): Show |
A | 1 | a0001c0001t0002g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.743+2272_743+2300d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949015 | ||||||
| chr8:53949030 | T | C | 1 | a0001c0001t0002g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.743+2282T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949030 | |||||||
| chr8:53949038 | T | C | 1 | a0001c0001t0002g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.743+2290T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949038 | |||||||
| chr8:53949043 | G | A | 12 | a0001c0001t0002g0032 a0001c0001t0002g0094 a0001c0001t0002g0117 others(9): Show |
12 | HG00597.hp2 HG00741.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+2295G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949043 | |||||||
| chr8:53949044 | C | CTA | 14 | a0001c0001t0001g0089 a0001c0001t0002g0032 a0001c0001t0002g0094 others(11): Show |
14 | HG00423.hp2 HG00597.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.743+2301_743+2302d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949044 | ||||||
| chr8:53949044 | C | CTATATAT others(28): Show |
1 | a0001c0001t0002g0203 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.743+2302_743+2303i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949044 | ||||||
| chr8:53949046 | ATATAAGA others(22): Show |
A | 3 | a0001c0001t0001g0198 a0001c0001t0002g0154 a0001c0001t0002g0258 |
3 | HG00642.hp1 HG01261.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.743+2303_743+2331d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949046 | ||||||
| chr8:53949069 | T | C | 2 | a0001c0001t0002g0104 a0001c0001t0002g0217 |
2 | HG01243.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.743+2321T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949069 | |||||||
| chr8:53949074 | G | A | 31 | a0001c0001t0001g0093 a0001c0001t0001g0163 a0001c0001t0002g0032 others(28): Show |
31 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.743+2326G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949074 | |||||||
| chr8:53949075 | C | CTA | 29 | a0001c0001t0001g0065 a0001c0001t0001g0072 a0001c0001t0001g0081 others(26): Show |
29 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.743+2332_743+2333d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949075 | ||||||
| chr8:53949075 | C | CTATATAT others(28): Show |
11 | a0001c0001t0001g0093 a0001c0001t0002g0129 a0001c0001t0002g0133 others(8): Show |
11 | HG00639.hp1 HG01109.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.743+2333_743+2334i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949075 | ||||||
| chr8:53949077 | ATATAAGA others(22): Show |
A | 23 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
23 | HG00597.hp1 HG01074.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.743+2334_743+2362d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949077 | ||||||
| chr8:53949105 | G | A | 55 | a0001c0001t0001g0023 a0001c0001t0001g0055 a0001c0001t0001g0089 others(52): Show |
55 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.743+2357G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949105 | |||||||
| chr8:53949106 | C | CTA | 53 | a0001c0001t0001g0048 a0001c0001t0001g0055 a0001c0001t0001g0061 others(50): Show |
53 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.743+2363_743+2364d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949106 | ||||||
| chr8:53949106 | C | CTATATAT others(28): Show |
3 | a0001c0001t0001g0105 a0001c0001t0001g0120 a0001c0001t0001g0229 |
3 | NA18988.hp2 NA19077.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.743+2364_743+2365i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949106 | ||||||
| chr8:53949106 | C | CTATATAT others(61): Show |
1 | a0001c0001t0002g0164 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.743+2364_743+2365i others(70): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949106 | ||||||
| chr8:53949108 | ATATAAGA others(22): Show |
A | 13 | a0001c0001t0001g0023 a0001c0001t0002g0196 a0001c0001t0003g0001 others(10): Show |
13 | HG01257.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.743+2365_743+2393d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949108 | ||||||
| chr8:53949136 | G | A | 81 | a0001c0001t0001g0031 a0001c0001t0001g0036 a0001c0001t0001g0040 others(78): Show |
81 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.743+2388G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949136 | |||||||
| chr8:53949137 | C | CTA | 94 | a0001c0001t0001g0018 a0001c0001t0001g0031 a0001c0001t0001g0035 others(91): Show |
94 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.743+2394_743+2395d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949137 | ||||||
| chr8:53949137 | C | CTATATAT others(28): Show |
1 | a0001c0001t0001g0081 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.743+2395_743+2396i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949137 | ||||||
| chr8:53949139 | ATATAAGA others(22): Show |
A | 12 | a0001c0001t0001g0068 a0001c0001t0001g0077 a0001c0001t0001g0121 others(9): Show |
12 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.743+2396_743+2424d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949139 | ||||||
| chr8:53949167 | G | A | 123 | a0001c0001t0001g0023 a0001c0001t0001g0031 a0001c0001t0001g0036 others(120): Show |
123 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.743+2419G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949167 | |||||||
| chr8:53949168 | C | CTA | 188 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(185): Show |
188 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.743+2425_743+2426d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949168 | ||||||
| chr8:53949168 | C | CTATATAT others(61): Show |
1 | a0001c0001t0001g0222 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.743+2426_743+2427i others(70): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949168 | ||||||
| chr8:53949170 | ATATAAGA others(22): Show |
A | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.743+2427_743+2455d others(31): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949170 | ||||||
| chr8:53949198 | G | A | 151 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0023 others(148): Show |
151 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.743+2450G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949198 | |||||||
| chr8:53949199 | C | CTA | 204 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.743+2456_743+2457d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | ||||||
| chr8:53949199 | C | CTATATAA others(191): Show |
1 | a0001c0001t0002g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.743+2571_743+2572i others(200): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | ||||||
| chr8:53949199 | C | CTATATAA others(191): Show |
1 | a0001c0001t0011g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.743+2483_743+2484i others(200): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | ||||||
| chr8:53949199 | C | CTATATAA others(26): Show |
1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743+2480_743+2481i others(35): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | ||||||
| chr8:53949199 | C | CTATATAT others(28): Show |
2 | a0001c0001t0001g0256 a0001c0001t0003g0022 |
2 | HG03471.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.743+2457_743+2458i others(37): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | ||||||
| chr8:53949199 | C | CTATATAT others(61): Show |
3 | a0001c0001t0002g0156 a0001c0001t0002g0199 a0001c0001t0002g0247 |
3 | HG01346.hp1 HG02273.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.743+2457_743+2458i others(70): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | ||||||
| chr8:53949199 | CTATATAA others(26): Show |
C | 1 | a0001c0001t0002g0135 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.743+2539_743+2571d others(35): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949199 | ||||||
| chr8:53949229 | A | G | 25 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0042 others(22): Show |
25 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.743+2481A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949229 | |||||||
| chr8:53949236 | A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+2488A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949236 | |||||||
| chr8:53949250 | A | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+2502A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949250 | |||||||
| chr8:53949262 | A | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0074 others(1): Show |
4 | HG00609.hp2 HG01496.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+2514A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949262 | |||||||
| chr8:53949269 | A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+2521A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949269 | |||||||
| chr8:53949283 | A | C | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+2535A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949283 | |||||||
| chr8:53949295 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.743+2547A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949295 | |||||||
| chr8:53949404 | A | T | 2 | a0001c0001t0002g0227 a0001c0001t0002g0228 |
2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.743+2656A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949404 | |||||||
| chr8:53949418 | A | G | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.743+2670A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949418 | |||||||
| chr8:53949425 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.743+2677A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949425 | |||||||
| chr8:53949542 | C | T | 2 | a0001c0001t0006g0043 a0001c0001t0006g0044 |
2 | HG01069.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.743+2794C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949542 | |||||||
| chr8:53949572 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.743+2824G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949572 | |||||||
| chr8:53949718 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.743+2970A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949718 | |||||||
| chr8:53949845 | C | CT | 141 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(138): Show |
141 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.743+3109dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53949845 | ||||||
| chr8:53949874 | C | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+3126C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53949874 | |||||||
| chr8:53950130 | A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.743+3382A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950130 | |||||||
| chr8:53950172 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.743+3424A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950172 | |||||||
| chr8:53950376 | C | T | 4 | a0001c0001t0002g0235 a0001c0001t0005g0118 a0001c0001t0005g0119 others(1): Show |
4 | HG01109.hp2 HG02055.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.743+3628C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950376 | |||||||
| chr8:53950441 | G | A | 181 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(178): Show |
181 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.744-3635G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950441 | |||||||
| chr8:53950620 | GT | G | 8 | a0001c0001t0001g0112 a0001c0001t0001g0116 a0001c0001t0001g0197 others(5): Show |
8 | HG00323.hp2 HG01109.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.744-3443delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53950620 | ||||||
| chr8:53950836 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.744-3240A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950836 | |||||||
| chr8:53950853 | G | A | 2 | a0001c0001t0005g0118 a0001c0001t0005g0119 |
2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.744-3223G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950853 | |||||||
| chr8:53950933 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.744-3143C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53950933 | |||||||
| chr8:53951348 | C | T | 6 | a0001c0001t0002g0106 a0001c0001t0002g0232 a0001c0001t0004g0037 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-2728C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53951348 | |||||||
| chr8:53951405 | A | G | 2 | a0001c0001t0003g0030 a0001c0001t0003g0169 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.744-2671A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53951405 | |||||||
| chr8:53951888 | C | G | 3 | a0001c0001t0005g0118 a0001c0001t0005g0119 a0001c0003t0002g0025 |
3 | HG02055.hp1 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.744-2188C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53951888 | |||||||
| chr8:53951909 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.744-2167C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53951909 | |||||||
| chr8:53951973 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.744-2103C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53951973 | |||||||
| chr8:53952171 | G | A | 12 | a0001c0001t0001g0041 a0001c0001t0001g0064 a0001c0001t0001g0068 others(9): Show |
12 | HG00438.hp2 HG02165.hp2 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.744-1905G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952171 | |||||||
| chr8:53952244 | A | AT | 43 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0001g0076 others(40): Show |
43 | HG00639.hp2 HG01109.hp2 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.744-1811dupT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53952244 | ||||||
| chr8:53952244 | A | ATT | 6 | a0001c0001t0002g0020 a0001c0001t0002g0168 a0001c0001t0002g0195 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.744-1812_744-1811d others(4): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53952244 | ||||||
| chr8:53952244 | AT | A | 13 | a0001c0001t0002g0106 a0001c0001t0002g0232 a0001c0001t0002g0237 others(10): Show |
13 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.744-1811delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53952244 | ||||||
| chr8:53952297 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.744-1779C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952297 | |||||||
| chr8:53952483 | C | T | 6 | a0001c0001t0002g0131 a0001c0001t0002g0139 a0001c0001t0002g0184 others(3): Show |
6 | HG01070.hp1 HG01975.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.744-1593C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952483 | |||||||
| chr8:53952590 | G | A | 180 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.744-1486G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952590 | |||||||
| chr8:53952657 | C | T | 2 | a0001c0001t0003g0030 a0001c0001t0003g0169 |
2 | HG02630.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.744-1419C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952657 | |||||||
| chr8:53952681 | G | A | 119 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0018 others(116): Show |
119 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.744-1395G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952681 | |||||||
| chr8:53952864 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.744-1212T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952864 | |||||||
| chr8:53952876 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.744-1200G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952876 | |||||||
| chr8:53952969 | T | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0123 |
2 | NA18945.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.744-1107T>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952969 | |||||||
| chr8:53952972 | A | G | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.744-1104A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53952972 | |||||||
| chr8:53953300 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.744-776C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53953300 | |||||||
| chr8:53953484 | G | T | 1 | a0001c0001t0009g0136 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.744-592G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53953484 | |||||||
| chr8:53953520 | C | CA | 214 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(211): Show |
214 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.744-544dupA | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr8 | 53953520 | ||||||
| chr8:53953588 | C | T | 166 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(163): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.744-488C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53953588 | |||||||
| chr8:53953622 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.744-454T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53953622 | |||||||
| chr8:53953931 | C | A | 166 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(163): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.744-145C>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 4/5 | chr8 | 53953931 | |||||||
| chr8:53954430 | G | T | 1 | a0001c0001t0002g0194 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.978+120G>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53954430 | |||||||
| chr8:53954489 | C | T | 1 | a0001c0001t0002g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.978+179C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53954489 | |||||||
| chr8:53954689 | CT | C | 45 | a0001c0001t0001g0059 a0001c0001t0002g0094 a0001c0001t0002g0117 others(42): Show |
45 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.978+395delT | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 53954689 | ||||||
| chr8:53954716 | C | T | 1 | a0001c0003t0002g0025 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.978+406C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53954716 | |||||||
| chr8:53954727 | G | A | 21 | a0001c0001t0002g0016 a0001c0001t0002g0020 a0001c0001t0002g0038 others(18): Show |
21 | HG01192.hp2 HG01891.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.978+417G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53954727 | |||||||
| chr8:53954845 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.978+535G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53954845 | |||||||
| chr8:53954982 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.978+672G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53954982 | |||||||
| chr8:53955057 | C | T | 4 | a0001c0001t0002g0133 a0001c0001t0006g0043 a0001c0001t0006g0044 others(1): Show |
4 | HG01069.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.978+747C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955057 | |||||||
| chr8:53955209 | T | C | 54 | a0001c0001t0002g0016 a0001c0001t0002g0020 a0001c0001t0002g0021 others(51): Show |
54 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.978+899T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955209 | |||||||
| chr8:53955499 | T | C | 2 | a0001c0001t0009g0128 a0001c0001t0009g0136 |
2 | HG04184.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.978+1189T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955499 | |||||||
| chr8:53955612 | C | G | 2 | a0001c0001t0002g0195 a0001c0001t0002g0240 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.978+1302C>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955612 | |||||||
| chr8:53955721 | C | T | 35 | a0001c0001t0001g0031 a0001c0001t0001g0035 a0001c0001t0001g0036 others(32): Show |
35 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.978+1411C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955721 | |||||||
| chr8:53955787 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.978+1477C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955787 | |||||||
| chr8:53955913 | T | C | 123 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(120): Show |
123 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.978+1603T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955913 | |||||||
| chr8:53955938 | G | A | 54 | a0001c0001t0002g0016 a0001c0001t0002g0020 a0001c0001t0002g0021 others(51): Show |
54 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.978+1628G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53955938 | |||||||
| chr8:53956239 | G | C | 7 | a0001c0001t0002g0020 a0001c0001t0002g0038 a0001c0001t0002g0108 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+1929G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956239 | |||||||
| chr8:53956246 | A | G | 177 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0015 others(174): Show |
177 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.978+1936A>G | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956246 | |||||||
| chr8:53956264 | A | T | 2 | a0001c0001t0002g0021 a0001c0001t0011g0208 |
2 | HG02109.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.978+1954A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956264 | |||||||
| chr8:53956471 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.979-1799G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956471 | |||||||
| chr8:53956490 | A | C | 15 | a0001c0001t0002g0106 a0001c0001t0002g0176 a0001c0001t0002g0232 others(12): Show |
15 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.979-1780A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956490 | |||||||
| chr8:53956592 | T | A | 1 | a0001c0001t0002g0178 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.979-1678T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956592 | |||||||
| chr8:53956643 | C | T | 1 | a0001c0001t0002g0243 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.979-1627C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956643 | |||||||
| chr8:53956730 | T | A | 1 | a0001c0001t0002g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.979-1540T>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956730 | |||||||
| chr8:53956905 | T | C | 1 | a0001c0002t0003g0003 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.979-1365T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956905 | |||||||
| chr8:53956913 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.979-1357C>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53956913 | |||||||
| chr8:53957124 | A | ATTTTG | 15 | a0001c0001t0003g0001 a0001c0001t0003g0024 a0001c0001t0003g0030 others(12): Show |
15 | HG01168.hp2 HG01169.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.979-1131_979-1127d others(7): Show |
RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr8 | 53957124 | ||||||
| chr8:53957320 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.979-950G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957320 | |||||||
| chr8:53957393 | G | C | 55 | a0001c0001t0002g0016 a0001c0001t0002g0020 a0001c0001t0002g0021 others(52): Show |
55 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.979-877G>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957393 | |||||||
| chr8:53957442 | T | C | 7 | a0001c0001t0002g0053 a0001c0001t0002g0070 a0001c0001t0002g0167 others(4): Show |
7 | HG01099.hp1 HG01496.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.979-828T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957442 | |||||||
| chr8:53957675 | T | C | 1 | a0001c0005t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.979-595T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957675 | |||||||
| chr8:53957783 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0095 a0001c0001t0001g0190 |
3 | HG00621.hp1 HG02040.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.979-487T>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957783 | |||||||
| chr8:53957945 | G | A | 2 | a0001c0001t0002g0129 a0001c0001t0002g0158 |
2 | NA18955.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.979-325G>A | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53957945 | |||||||
| chr8:53958168 | A | C | 1 | a0001c0001t0002g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.979-102A>C | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53958168 | |||||||
| chr8:53958206 | A | T | 1 | a0001c0001t0001g0090 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.979-64A>T | RGS20 | ENSG00000147509.14 | transcript | ENST00000297313.8 | protein_coding | 5/5 | chr8 | 53958206 |