Item | Value |
---|---|
geneid | 6256 |
ensemblid | ENSG00000186350.12 |
hgncid | 10477 |
symbol | RXRA |
name | retinoid X receptor alpha |
refseq_nuc | NM_002957.6 |
refseq_prot | NP_002948.1 |
ensembl_nuc | ENST00000481739.2 |
ensembl_prot | ENSP00000419692.1 |
mane_status | MANE Select |
chr | chr9 |
start | 134326455 |
end | 134440585 |
strand | + |
ver | v1.2 |
region | chr9:134326455-134440585 |
region5000 | chr9:134321455-134445585 |
regionname0 | RXRA_chr9_134326455_134440585 |
regionname5000 | RXRA_chr9_134321455_134445585 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1386 | 227 | 83 | 51 | 57 | 8 | 26 | RXRA_chr9_134321455_134445585 | RXRA | ATGGA others(1381): Show |
chr9 | 134321455 | 134445585 | ||
a0001c0002 | 0/0 | 1386 | 2 | 0 | 2 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | ATGGA others(1381): Show |
chr9 | 134321455 | 134445585 | ||
a0001c0003 | 0/0 | 1386 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | ATGGA others(1381): Show |
chr9 | 134321455 | 134445585 | ||
a0001c0004 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | ATGGA others(1381): Show |
chr9 | 134321455 | 134445585 | ||
a0001c0005 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | ATGGA others(1381): Show |
chr9 | 134321455 | 134445585 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5533 | 57 | 7 | 17 | 20 | 5 | 8 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0002 | 0/1 | 5533 | 33 | 1 | 8 | 12 | 0 | 11 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0003 | 0/0 | 5533 | 15 | 1 | 9 | 4 | 1 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0004 | 0/0 | 5533 | 14 | 13 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0005 | 0/0 | 5534 | 11 | 2 | 0 | 6 | 0 | 3 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5529): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0006 | 0/0 | 5533 | 6 | 0 | 6 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0007 | 0/0 | 5532 | 5 | 4 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5527): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0008 | 0/0 | 5533 | 5 | 5 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0009 | 0/0 | 5539 | 5 | 5 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5534): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0010 | 0/0 | 5533 | 4 | 3 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0011 | 0/0 | 5533 | 4 | 4 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0012 | 0/0 | 5533 | 4 | 3 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0013 | 0/0 | 5533 | 2 | 0 | 0 | 2 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0014 | 0/0 | 5532 | 3 | 3 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5527): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0015 | 0/0 | 5533 | 3 | 3 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0016 | 0/0 | 5540 | 3 | 3 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5535): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0017 | 0/0 | 5533 | 3 | 0 | 0 | 3 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0018 | 0/0 | 5533 | 2 | 0 | 0 | 2 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0019 | 0/0 | 5533 | 2 | 0 | 0 | 2 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0020 | 0/0 | 5533 | 2 | 2 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0021 | 0/0 | 5545 | 2 | 0 | 2 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5540): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0022 | 0/0 | 5540 | 2 | 2 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5535): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0023 | 0/0 | 5532 | 2 | 2 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5527): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0024 | 0/0 | 5560 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5555): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0025 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0026 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0027 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0028 | 0/0 | 5533 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0029 | 0/0 | 5534 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5529): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0030 | 0/0 | 5533 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0031 | 0/0 | 5533 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0032 | 0/0 | 5533 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0033 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5527): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0034 | 0/0 | 5533 | 1 | 0 | 0 | 0 | 1 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0035 | 0/0 | 5533 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0036 | 0/0 | 5533 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0037 | 0/0 | 5533 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0038 | 0/0 | 5533 | 1 | 0 | 0 | 0 | 1 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0039 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0041 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0042 | 1/0 | 5537 | 1 | 0 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5532): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0043 | 0/0 | 5538 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5533): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0044 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5527): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0045 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5527): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0046 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5529): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0047 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5529): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0048 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0049 | 0/0 | 5533 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0050 | 0/0 | 5533 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0051 | 0/0 | 5532 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5527): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0052 | 0/0 | 5533 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0053 | 0/0 | 5533 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0054 | 0/0 | 5536 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5531): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0055 | 0/0 | 5537 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5532): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0056 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0057 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0058 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0059 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0060 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5529): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0061 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0001t0062 | 0/0 | 5533 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0002t0002 | 0/0 | 5533 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0002t0040 | 0/0 | 5602 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5597): Show |
chr9 | 134321455 | 134445585 |
a0001c0003t0013 | 0/0 | 5533 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
a0001c0004t0005 | 0/0 | 5534 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5529): Show |
chr9 | 134321455 | 134445585 |
a0001c0005t0001 | 0/0 | 5533 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | AGTTT others(5528): Show |
chr9 | 134321455 | 134445585 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0006g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0006g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0006g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0009g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0010g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0010g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0010g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0011g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0011g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0011g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0012g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0012g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0013g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0013g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0014g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0014g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0014g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0015g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0015g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0016g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0016g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0016g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0017g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0017g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0017g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0018g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0018g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0019g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0019g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0020g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0020g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0021g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0021g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0022g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0022g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0023g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0023g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0024g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0025g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0026g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0027g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0028g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0029g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0030g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0031g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0032g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0033g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0034g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0035g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0036g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0037g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0038g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0039g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0041g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0042g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0043g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0044g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0045g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0046g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0047g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0048g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0049g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0050g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0051g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0052g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0053g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0054g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0055g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0056g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0057g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0058g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0059g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0060g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0061g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0001t0062g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0002t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0002t0040g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0003t0013g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0004t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
a0001c0005t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0038 | g0074 | EUR | GBR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | GBR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0049 | EUR | GBR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | GBR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0183 | EAS | CHS | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00621 | hp1 | a0001 | c0001 | t0017 | g0057 | EAS | CHS | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00642 | hp2 | a0001 | c0001 | t0036 | g0201 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0202 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0177 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01070 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01074 | hp1 | a0001 | c0001 | t0054 | g0018 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01109 | hp1 | a0001 | c0001 | t0012 | g0162 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01169 | hp1 | a0001 | c0001 | t0037 | g0061 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01255 | hp1 | a0001 | c0001 | t0032 | g0017 | AMR | CLM | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01255 | hp2 | a0001 | c0002 | t0040 | g0040 | AMR | CLM | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0181 | AMR | CLM | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01257 | hp1 | a0001 | c0001 | t0055 | g0167 | AMR | CLM | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01346 | hp1 | a0001 | c0001 | t0021 | g0106 | AMR | CLM | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01433 | hp2 | a0001 | c0001 | t0028 | g0109 | AMR | CLM | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01884 | hp1 | a0001 | c0001 | t0012 | g0038 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01884 | hp2 | a0001 | c0001 | t0011 | g0132 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0147 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01891 | hp2 | a0001 | c0001 | t0011 | g0121 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01943 | hp2 | a0001 | c0001 | t0010 | g0163 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01978 | hp1 | a0001 | c0001 | t0021 | g0047 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02027 | hp1 | a0001 | c0001 | t0019 | g0059 | EAS | KHV | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02040 | hp2 | a0001 | c0001 | t0005 | g0144 | EAS | KHV | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02055 | hp2 | a0001 | c0001 | t0012 | g0151 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02083 | hp2 | a0001 | c0001 | t0005 | g0184 | EAS | KHV | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02145 | hp2 | a0001 | c0001 | t0014 | g0180 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CDX | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02257 | hp2 | a0001 | c0001 | t0016 | g0207 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02258 | hp1 | a0001 | c0001 | t0010 | g0101 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02258 | hp2 | a0001 | c0001 | t0007 | g0203 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02280 | hp2 | a0001 | c0001 | t0024 | g0172 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02293 | hp1 | a0001 | c0003 | t0013 | g0034 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0039 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0037 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02451 | hp2 | a0001 | c0001 | t0015 | g0168 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02615 | hp1 | a0001 | c0001 | t0059 | g0210 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02615 | hp2 | a0001 | c0001 | t0016 | g0155 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0209 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02647 | hp1 | a0001 | c0001 | t0045 | g0161 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0138 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0176 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02717 | hp1 | a0001 | c0001 | t0062 | g0120 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0087 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0131 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02723 | hp2 | a0001 | c0001 | t0015 | g0102 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0090 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02809 | hp2 | a0001 | c0001 | t0051 | g0023 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0130 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02886 | hp1 | a0001 | c0001 | t0012 | g0159 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02886 | hp2 | a0001 | c0001 | t0016 | g0115 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02895 | hp1 | a0001 | c0001 | t0009 | g0098 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02896 | hp2 | a0001 | c0001 | t0023 | g0150 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02897 | hp2 | a0001 | c0001 | t0023 | g0149 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02965 | hp1 | a0001 | c0001 | t0048 | g0024 | AFR | ESN | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02965 | hp2 | a0001 | c0001 | t0025 | g0158 | AFR | ESN | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0133 | AFR | ESN | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02970 | hp2 | a0001 | c0001 | t0046 | g0152 | AFR | ESN | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02976 | hp1 | a0001 | c0001 | t0020 | g0154 | AFR | ESN | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02976 | hp2 | a0001 | c0004 | t0005 | g0126 | AFR | ESN | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03041 | hp2 | a0001 | c0001 | t0041 | g0139 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03139 | hp2 | a0001 | c0001 | t0022 | g0134 | AFR | ESN | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03195 | hp1 | a0001 | c0001 | t0014 | g0173 | AFR | ESN | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03195 | hp2 | a0001 | c0001 | t0008 | g0125 | AFR | ESN | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0119 | AFR | MSL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03225 | hp2 | a0001 | c0001 | t0061 | g0156 | AFR | MSL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03453 | hp1 | a0001 | c0001 | t0009 | g0137 | AFR | MSL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | MSL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03486 | hp1 | a0001 | c0001 | t0056 | g0143 | AFR | MSL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03490 | hp1 | a0001 | c0001 | t0035 | g0007 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03516 | hp1 | a0001 | c0001 | t0008 | g0141 | AFR | ESN | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03516 | hp2 | a0001 | c0001 | t0044 | g0136 | AFR | ESN | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03540 | hp1 | a0001 | c0001 | t0009 | g0157 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | GWD | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03669 | hp2 | a0001 | c0001 | t0052 | g0012 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | BEB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | BEB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03927 | hp2 | a0001 | c0001 | t0053 | g0006 | SAS | BEB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | STU | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | STU | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | STU | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0020 | SAS | STU | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0189 | SAS | STU | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG04228 | hp2 | a0001 | c0001 | t0049 | g0041 | SAS | STU | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18522 | hp1 | a0001 | c0001 | t0039 | g0206 | AFR | YRI | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18522 | hp2 | a0001 | c0001 | t0020 | g0182 | AFR | YRI | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18906 | hp1 | a0001 | c0001 | t0058 | g0117 | AFR | YRI | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18906 | hp2 | a0001 | c0001 | t0022 | g0208 | AFR | YRI | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18939 | hp2 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18944 | hp2 | a0001 | c0001 | t0018 | g0105 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18947 | hp1 | a0001 | c0001 | t0013 | g0188 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18947 | hp2 | a0001 | c0001 | t0029 | g0026 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18964 | hp2 | a0001 | c0001 | t0019 | g0190 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18995 | hp2 | a0001 | c0001 | t0013 | g0197 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19004 | hp2 | a0001 | c0001 | t0017 | g0186 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19009 | hp2 | a0001 | c0001 | t0031 | g0065 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19010 | hp2 | a0001 | c0001 | t0030 | g0033 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19030 | hp1 | a0001 | c0001 | t0027 | g0086 | AFR | LWK | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19043 | hp1 | a0001 | c0001 | t0011 | g0099 | AFR | LWK | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19043 | hp2 | a0001 | c0001 | t0060 | g0100 | AFR | LWK | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19068 | hp1 | a0001 | c0001 | t0007 | g0035 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19079 | hp2 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19080 | hp2 | a0001 | c0001 | t0018 | g0104 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19090 | hp1 | a0001 | c0005 | t0001 | g0193 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19090 | hp2 | a0001 | c0001 | t0017 | g0058 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19240 | hp1 | a0001 | c0001 | t0047 | g0116 | AFR | YRI | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA19240 | hp2 | a0001 | c0001 | t0015 | g0114 | AFR | YRI | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA20752 | hp1 | a0001 | c0001 | t0034 | g0011 | EUR | TSI | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | TSI | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0221 | EUR | TSI | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02109 | hp2 | a0001 | c0001 | t0011 | g0140 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02486 | hp1 | a0001 | c0001 | t0010 | g0213 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02559 | hp1 | a0001 | c0001 | t0010 | g0122 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG02559 | hp2 | a0001 | c0001 | t0057 | g0053 | AFR | ACB | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03471 | hp1 | a0001 | c0001 | t0014 | g0085 | AFR | MSL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | USA | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0204 | AFR | USA | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18955 | hp1 | a0001 | c0001 | t0050 | g0042 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA18955 | hp2 | a0001 | c0001 | t0043 | g0004 | EAS | JPT | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | USA | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0160 | AFR | USA | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA21309 | hp1 | a0001 | c0001 | t0026 | g0127 | AFR | LWK | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
NA21309 | hp2 | a0001 | c0001 | t0033 | g0171 | AFR | LWK | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0072 | REF | REF | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
homoSapiens | grch38p0 | a0001 | c0001 | t0042 | g0063 | REF | REF | RXRA_chr9_134321455_134445585 | RXRA | chr9 | 134321455 | 134445585 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:134408157 | A | G | 1 | a0001c0005 | 1 | NA19090.hp1 | synonymous_variant | LOW | c.288A>G | p.Ser96Ser | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 3/10 | 465/5537 | 288/1389 | 96/462 | chr9 | 134408157 | |||
chr9:134417213 | G | A | 1 | a0001c0003 | 1 | HG02293.hp1 | synonymous_variant | LOW | c.666G>A | p.Ser222Ser | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/10 | 843/5537 | 666/1389 | 222/462 | chr9 | 134417213 | |||
chr9:134431974 | C | T | 1 | a0001c0004 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1113C>T | p.Arg371Arg | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/10 | 1290/5537 | 1113/1389 | 371/462 | chr9 | 134431974 | |||
chr9:134436596 | G | A | 1 | a0001c0002 | 2 | HG01169.hp2 HG01255.hp2 |
synonymous_variant | LOW | c.1371G>A | p.Ala457Ala | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1548/5537 | 1371/1389 | 457/462 | chr9 | 134436596 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:134326505 | C | T | 1 | a0001c0001t0062 | 1 | HG02717.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-127C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/10 | chr9 | 134326505 | |||||||
chr9:134326580 | C | CGCCCGCC others(20): Show |
1 | a0001c0001t0024 | 1 | HG02280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48_-22dupCGCCGCCC others(19): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/10 | 21 | INFO_REALIGN_3_PRIME | chr9 | 134326580 | |||||
chr9:134326610 | C | T | 1 | a0001c0001t0061 | 1 | HG03225.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-22C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/10 | chr9 | 134326610 | |||||||
chr9:134436854 | C | T | 1 | a0001c0001t0023 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*240C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 240 | chr9 | 134436854 | ||||||
chr9:134436908 | C | G | 1 | a0001c0001t0017 | 3 | HG00621.hp1 NA19004.hp2 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*294C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 294 | chr9 | 134436908 | ||||||
chr9:134436987 | G | A | 3 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0062 |
3 | HG02717.hp1 HG02965.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*373G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 373 | chr9 | 134436987 | ||||||
chr9:134437099 | CT | C | 1 | a0001c0001t0023 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*486delT | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 486 | chr9 | 134437099 | ||||||
chr9:134437198 | G | A | 1 | a0001c0001t0027 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*584G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 584 | chr9 | 134437198 | ||||||
chr9:134437383 | C | T | 1 | a0001c0001t0060 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*769C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 769 | chr9 | 134437383 | ||||||
chr9:134437391 | C | T | 1 | a0001c0001t0059 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*777C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 777 | chr9 | 134437391 | ||||||
chr9:134437460 | G | A | 17 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(14): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*846G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 846 | chr9 | 134437460 | ||||||
chr9:134437567 | G | C | 2 | a0001c0001t0039 a0001c0001t0061 |
2 | HG03225.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*953G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 953 | chr9 | 134437567 | ||||||
chr9:134437575 | C | T | 2 | a0001c0001t0009 a0001c0001t0022 |
7 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*961C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 961 | chr9 | 134437575 | ||||||
chr9:134437644 | A | G | 1 | a0001c0001t0026 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1030A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1030 | chr9 | 134437644 | ||||||
chr9:134437687 | C | T | 4 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0022 others(1): Show |
11 | HG02257.hp2 HG02615.hp2 HG02647.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1073C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1073 | chr9 | 134437687 | ||||||
chr9:134437702 | C | T | 1 | a0001c0001t0023 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1088C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1088 | chr9 | 134437702 | ||||||
chr9:134437713 | C | T | 4 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0022 others(1): Show |
11 | HG02257.hp2 HG02615.hp2 HG02647.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1099C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1099 | chr9 | 134437713 | ||||||
chr9:134437905 | C | T | 2 | a0001c0001t0015 a0001c0001t0059 |
4 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1291C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1291 | chr9 | 134437905 | ||||||
chr9:134437975 | G | GCGCTCCT | 3 | a0001c0001t0009 a0001c0001t0016 a0001c0001t0022 |
10 | HG02257.hp2 HG02615.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1363_*1369dupGCTC others(3): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1370 | INFO_REALIGN_3_PRIME | chr9 | 134437975 | |||||
chr9:134438007 | C | T | 1 | a0001c0001t0038 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1393C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1393 | chr9 | 134438007 | ||||||
chr9:134438092 | G | GACATCAG others(62): Show |
1 | a0001c0002t0040 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1478_*1479insACAT others(65): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1479 | chr9 | 134438092 | ||||||
chr9:134438093 | C | G | 1 | a0001c0001t0057 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1479C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1479 | chr9 | 134438093 | ||||||
chr9:134438150 | G | T | 1 | a0001c0001t0037 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1536G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1536 | chr9 | 134438150 | ||||||
chr9:134438223 | C | G | 1 | a0001c0001t0027 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1609C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1609 | chr9 | 134438223 | ||||||
chr9:134438291 | G | A | 6 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0011 others(3): Show |
28 | HG00735.hp2 HG01884.hp2 HG01891.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1677G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1677 | chr9 | 134438291 | ||||||
chr9:134438396 | A | G | 1 | a0001c0001t0060 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1782A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1782 | chr9 | 134438396 | ||||||
chr9:134438429 | A | G | 1 | a0001c0001t0036 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1815A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1815 | chr9 | 134438429 | ||||||
chr9:134438533 | G | A | 2 | a0001c0001t0010 a0001c0001t0020 |
6 | HG01943.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1919G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 1919 | chr9 | 134438533 | ||||||
chr9:134438666 | C | T | 1 | a0001c0001t0056 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2052C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2052 | chr9 | 134438666 | ||||||
chr9:134438699 | A | G | 2 | a0001c0001t0054 a0001c0001t0055 |
2 | HG01074.hp1 HG01257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2085A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2085 | chr9 | 134438699 | ||||||
chr9:134438714 | C | T | 18 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(15): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*2100C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2100 | chr9 | 134438714 | ||||||
chr9:134438761 | G | A | 1 | a0001c0001t0056 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2147G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2147 | chr9 | 134438761 | ||||||
chr9:134438818 | T | G | 2 | a0001c0001t0039 a0001c0001t0061 |
2 | HG03225.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2204T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2204 | chr9 | 134438818 | ||||||
chr9:134438834 | G | A | 1 | a0001c0001t0041 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2220G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2220 | chr9 | 134438834 | ||||||
chr9:134438842 | C | CGCTGGCT others(1): Show |
1 | a0001c0001t0021 | 2 | HG01346.hp1 HG01978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2245_*2252dupGCTG others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2253 | INFO_REALIGN_3_PRIME | chr9 | 134438842 | |||||
chr9:134438842 | CGCTG | C | 61 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(58): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*2249_*2252delGCTG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2249 | INFO_REALIGN_3_PRIME | chr9 | 134438842 | |||||
chr9:134438868 | A | T | 1 | a0001c0001t0043 | 1 | NA18955.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2254A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2254 | chr9 | 134438868 | ||||||
chr9:134438910 | C | T | 3 | a0001c0001t0006 a0001c0001t0035 a0001c0001t0052 |
8 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2296C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2296 | chr9 | 134438910 | ||||||
chr9:134438933 | C | A | 1 | a0001c0001t0022 | 2 | HG03139.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2319C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2319 | chr9 | 134438933 | ||||||
chr9:134438958 | G | A | 1 | a0001c0001t0012 | 4 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2344G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2344 | chr9 | 134438958 | ||||||
chr9:134439062 | T | A | 2 | a0001c0001t0044 a0001c0001t0045 |
2 | HG02647.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2448T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2448 | chr9 | 134439062 | ||||||
chr9:134439220 | C | G | 1 | a0001c0001t0034 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2606C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2606 | chr9 | 134439220 | ||||||
chr9:134439260 | C | A | 26 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(23): Show |
68 | HG00597.hp2 HG00735.hp2 HG01109.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2646C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2646 | chr9 | 134439260 | ||||||
chr9:134439263 | CA | C | 6 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0033 others(3): Show |
12 | HG02145.hp2 HG02647.hp1 HG02647.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2650delA | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2650 | chr9 | 134439263 | ||||||
chr9:134439264 | A | C | 26 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0008 others(23): Show |
68 | HG00597.hp2 HG00735.hp2 HG01109.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2650A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2650 | chr9 | 134439264 | ||||||
chr9:134439340 | G | A | 1 | a0001c0001t0014 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2726G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2726 | chr9 | 134439340 | ||||||
chr9:134439364 | C | T | 1 | a0001c0001t0051 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2750C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2750 | chr9 | 134439364 | ||||||
chr9:134439474 | C | T | 1 | a0001c0001t0052 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2860C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2860 | chr9 | 134439474 | ||||||
chr9:134439483 | G | A | 1 | a0001c0001t0060 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2869G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2869 | chr9 | 134439483 | ||||||
chr9:134439537 | G | A | 1 | a0001c0001t0049 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2923G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 2923 | chr9 | 134439537 | ||||||
chr9:134439639 | A | T | 7 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0015 others(4): Show |
25 | HG00735.hp2 HG01255.hp1 HG01943.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3025A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3025 | chr9 | 134439639 | ||||||
chr9:134439679 | G | C | 1 | a0001c0001t0028 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3065G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3065 | chr9 | 134439679 | ||||||
chr9:134439719 | G | T | 1 | a0001c0001t0055 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3105G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3105 | chr9 | 134439719 | ||||||
chr9:134439720 | T | G | 1 | a0001c0001t0055 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3106T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3106 | chr9 | 134439720 | ||||||
chr9:134439721 | G | T | 1 | a0001c0001t0055 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3107G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3107 | chr9 | 134439721 | ||||||
chr9:134439755 | G | A | 2 | a0001c0001t0029 a0001c0001t0030 |
2 | NA18947.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3141G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3141 | chr9 | 134439755 | ||||||
chr9:134439770 | C | T | 1 | a0001c0001t0047 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3156C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3156 | chr9 | 134439770 | ||||||
chr9:134439776 | A | G | 5 | a0001c0001t0004 a0001c0001t0010 a0001c0001t0015 others(2): Show |
23 | HG00735.hp2 HG01943.hp2 HG02055.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3162A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3162 | chr9 | 134439776 | ||||||
chr9:134439808 | G | A | 2 | a0001c0001t0013 a0001c0003t0013 |
3 | HG02293.hp1 NA18947.hp1 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3194G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3194 | chr9 | 134439808 | ||||||
chr9:134439981 | C | G | 1 | a0001c0001t0050 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3367C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3367 | chr9 | 134439981 | ||||||
chr9:134440049 | G | C | 1 | a0001c0001t0018 | 2 | NA18944.hp2 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3435G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3435 | chr9 | 134440049 | ||||||
chr9:134440091 | T | TA | 7 | a0001c0001t0005 a0001c0001t0029 a0001c0001t0043 others(4): Show |
17 | HG00597.hp2 HG01891.hp1 HG02040.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3489dupA | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3490 | INFO_REALIGN_3_PRIME | chr9 | 134440091 | |||||
chr9:134440091 | TA | T | 2 | a0001c0001t0007 a0001c0001t0054 |
6 | HG01074.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3489delA | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3489 | INFO_REALIGN_3_PRIME | chr9 | 134440091 | |||||
chr9:134440155 | G | A | 1 | a0001c0001t0044 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3541G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3541 | chr9 | 134440155 | ||||||
chr9:134440210 | C | T | 1 | a0001c0001t0048 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3596C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3596 | chr9 | 134440210 | ||||||
chr9:134440263 | C | T | 3 | a0001c0001t0005 a0001c0001t0043 a0001c0004t0005 |
13 | HG00597.hp2 HG01891.hp1 HG02040.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3649C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3649 | chr9 | 134440263 | ||||||
chr9:134440267 | G | A | 1 | a0001c0001t0009 | 5 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3653G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3653 | chr9 | 134440267 | ||||||
chr9:134440356 | G | A | 1 | a0001c0001t0044 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3742G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3742 | chr9 | 134440356 | ||||||
chr9:134440401 | T | C | 1 | a0001c0001t0035 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3787T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3787 | chr9 | 134440401 | ||||||
chr9:134440465 | T | G | 55 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(52): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*3851T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3851 | chr9 | 134440465 | ||||||
chr9:134440555 | G | A | 1 | a0001c0001t0019 | 2 | HG02027.hp1 NA18964.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3941G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 10/10 | 3941 | chr9 | 134440555 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:134326830 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.28+171C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134326830 | |||||||
chr9:134326956 | C | G | 1 | a0001c0001t0004g0225 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.28+297C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134326956 | |||||||
chr9:134326995 | C | T | 7 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0002g0219 others(4): Show |
7 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+336C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134326995 | |||||||
chr9:134327031 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.28+372C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134327031 | |||||||
chr9:134327085 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.28+426C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134327085 | |||||||
chr9:134327173 | C | A | 1 | a0001c0001t0053g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.28+514C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134327173 | |||||||
chr9:134327280 | C | G | 46 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0194 others(43): Show |
47 | HG00099.hp2 HG00597.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.28+621C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134327280 | |||||||
chr9:134327368 | T | C | 1 | a0001c0001t0014g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.28+709T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134327368 | |||||||
chr9:134327375 | C | T | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28+716C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134327375 | |||||||
chr9:134327763 | C | T | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.28+1104C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134327763 | |||||||
chr9:134327870 | CG | C | 3 | a0001c0001t0006g0002 a0001c0001t0035g0007 a0001c0002t0002g0008 |
4 | HG01070.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+1212delG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134327870 | |||||||
chr9:134328060 | T | C | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+1401T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328060 | |||||||
chr9:134328181 | G | C | 7 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0002g0219 others(4): Show |
7 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+1522G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328181 | |||||||
chr9:134328229 | A | G | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0015g0168 others(1): Show |
4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+1570A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328229 | |||||||
chr9:134328290 | A | G | 1 | a0001c0001t0055g0167 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.28+1631A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328290 | |||||||
chr9:134328299 | G | A | 1 | a0001c0001t0052g0012 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.28+1640G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328299 | |||||||
chr9:134328309 | C | A | 2 | a0001c0001t0001g0175 a0001c0001t0003g0174 |
2 | NA18969.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.28+1650C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328309 | |||||||
chr9:134328318 | C | T | 1 | a0001c0001t0010g0213 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.28+1659C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328318 | |||||||
chr9:134328444 | C | G | 1 | a0001c0001t0004g0225 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.28+1785C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328444 | |||||||
chr9:134328449 | G | T | 3 | a0001c0001t0003g0166 a0001c0001t0004g0225 a0001c0001t0005g0165 |
3 | HG01243.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+1790G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328449 | |||||||
chr9:134328473 | A | G | 1 | a0001c0001t0004g0225 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.28+1814A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328473 | |||||||
chr9:134328684 | C | T | 1 | a0001c0001t0002g0212 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.28+2025C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328684 | |||||||
chr9:134328697 | G | T | 19 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(16): Show |
21 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.28+2038G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328697 | |||||||
chr9:134328718 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0211 a0001c0001t0003g0174 |
3 | NA18967.hp2 NA18969.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.28+2059C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328718 | |||||||
chr9:134328770 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.28+2111G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328770 | |||||||
chr9:134328965 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.28+2306C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134328965 | |||||||
chr9:134329029 | G | A | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28+2370G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134329029 | |||||||
chr9:134329039 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.28+2380C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134329039 | |||||||
chr9:134329053 | A | G | 12 | a0001c0001t0004g0005 a0001c0001t0004g0202 a0001c0001t0004g0204 others(9): Show |
13 | HG00735.hp2 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.28+2394A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134329053 | |||||||
chr9:134329190 | G | A | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0015g0168 others(1): Show |
4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+2531G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134329190 | |||||||
chr9:134329233 | T | A | 1 | a0001c0001t0001g0014 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.28+2574T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134329233 | |||||||
chr9:134329317 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.28+2658G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134329317 | |||||||
chr9:134329324 | C | T | 18 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(15): Show |
20 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.28+2665C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134329324 | |||||||
chr9:134329405 | C | T | 1 | a0001c0001t0005g0144 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.28+2746C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134329405 | |||||||
chr9:134329591 | G | A | 46 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0194 others(43): Show |
47 | HG00099.hp2 HG00597.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.28+2932G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134329591 | |||||||
chr9:134329735 | C | T | 7 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0002g0219 others(4): Show |
7 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+3076C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134329735 | |||||||
chr9:134329736 | A | G | 126 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(123): Show |
130 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.28+3077A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134329736 | |||||||
chr9:134329802 | T | C | 107 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(104): Show |
111 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.28+3143T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134329802 | |||||||
chr9:134329823 | CTT | C | 15 | a0001c0001t0001g0135 a0001c0001t0003g0142 a0001c0001t0004g0128 others(12): Show |
15 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.28+3166_28+3167del others(2): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134329823 | ||||||
chr9:134330014 | T | C | 90 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(87): Show |
92 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.28+3355T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134330014 | |||||||
chr9:134330132 | C | G | 1 | a0001c0001t0002g0097 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.28+3473C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134330132 | |||||||
chr9:134330142 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.28+3483G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134330142 | |||||||
chr9:134330291 | G | A | 87 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(84): Show |
89 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.28+3632G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134330291 | |||||||
chr9:134330465 | A | G | 26 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0003g0142 others(23): Show |
28 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.28+3806A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134330465 | |||||||
chr9:134330607 | C | T | 2 | a0001c0001t0003g0166 a0001c0001t0005g0165 |
2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+3948C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134330607 | |||||||
chr9:134330838 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.28+4179T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134330838 | |||||||
chr9:134331097 | T | G | 3 | a0001c0001t0003g0166 a0001c0001t0004g0225 a0001c0001t0005g0165 |
3 | HG01243.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+4438T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331097 | |||||||
chr9:134331116 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.28+4457C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331116 | |||||||
chr9:134331127 | G | C | 3 | a0001c0001t0003g0166 a0001c0001t0004g0225 a0001c0001t0005g0165 |
3 | HG01243.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+4468G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331127 | |||||||
chr9:134331156 | A | G | 128 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(125): Show |
132 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(129): Show |
intron_variant | MODIFIER | c.28+4497A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331156 | |||||||
chr9:134331230 | C | T | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28+4571C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331230 | |||||||
chr9:134331394 | C | T | 85 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(82): Show |
87 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.28+4735C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331394 | |||||||
chr9:134331413 | G | C | 1 | a0001c0001t0032g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.28+4754G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331413 | |||||||
chr9:134331464 | T | A | 2 | a0001c0001t0004g0128 a0001c0001t0004g0129 |
2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.28+4805T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331464 | |||||||
chr9:134331478 | G | A | 3 | a0001c0001t0009g0098 a0001c0001t0011g0099 a0001c0001t0060g0100 |
3 | HG02895.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.28+4819G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331478 | |||||||
chr9:134331486 | G | A | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+4827G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331486 | |||||||
chr9:134331540 | T | C | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+4881T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331540 | |||||||
chr9:134331766 | T | C | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.28+5107T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331766 | |||||||
chr9:134331771 | G | GACACAAG others(1): Show |
115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+5112_28+5113ins others(8): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331771 | |||||||
chr9:134331826 | G | A | 19 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(16): Show |
21 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.28+5167G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331826 | |||||||
chr9:134331852 | C | T | 6 | a0001c0001t0001g0220 a0001c0001t0002g0219 a0001c0001t0002g0223 others(3): Show |
6 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.28+5193C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134331852 | |||||||
chr9:134332359 | G | A | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+5700G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134332359 | |||||||
chr9:134332484 | G | A | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+5825G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134332484 | |||||||
chr9:134332584 | A | G | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+5925A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134332584 | |||||||
chr9:134332648 | G | A | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+5989G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134332648 | |||||||
chr9:134332815 | C | T | 27 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(24): Show |
28 | HG00621.hp2 HG00733.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.28+6156C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134332815 | |||||||
chr9:134332826 | G | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG01928.hp1 HG01978.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+6167G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134332826 | |||||||
chr9:134332845 | G | A | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+6186G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134332845 | |||||||
chr9:134332924 | C | T | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.28+6265C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134332924 | |||||||
chr9:134332935 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.28+6276A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134332935 | |||||||
chr9:134333025 | C | A | 19 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(16): Show |
21 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.28+6366C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333025 | |||||||
chr9:134333064 | C | T | 114 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(111): Show |
118 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.28+6405C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333064 | |||||||
chr9:134333077 | T | C | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+6418T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333077 | |||||||
chr9:134333101 | C | T | 3 | a0001c0001t0003g0166 a0001c0001t0004g0225 a0001c0001t0005g0165 |
3 | HG01243.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+6442C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333101 | |||||||
chr9:134333122 | A | G | 6 | a0001c0001t0001g0220 a0001c0001t0002g0219 a0001c0001t0002g0223 others(3): Show |
6 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.28+6463A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333122 | |||||||
chr9:134333136 | A | G | 1 | a0001c0001t0036g0201 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.28+6477A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333136 | |||||||
chr9:134333257 | A | T | 128 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(125): Show |
132 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(129): Show |
intron_variant | MODIFIER | c.28+6598A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333257 | |||||||
chr9:134333311 | G | A | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+6652G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333311 | |||||||
chr9:134333357 | G | C | 31 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(28): Show |
32 | HG00621.hp2 HG00733.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.28+6698G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333357 | |||||||
chr9:134333371 | C | T | 114 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(111): Show |
118 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.28+6712C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333371 | |||||||
chr9:134333378 | C | T | 1 | a0001c0001t0010g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28+6719C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333378 | |||||||
chr9:134333396 | A | G | 1 | a0001c0001t0004g0129 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.28+6737A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333396 | |||||||
chr9:134333486 | G | A | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+6827G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333486 | |||||||
chr9:134333508 | C | T | 45 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0194 others(42): Show |
46 | HG00099.hp2 HG00597.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.28+6849C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333508 | |||||||
chr9:134333527 | T | A | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+6868T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333527 | |||||||
chr9:134333548 | C | T | 2 | a0001c0001t0026g0127 a0001c0004t0005g0126 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28+6889C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333548 | |||||||
chr9:134333584 | C | T | 1 | a0001c0001t0007g0090 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.28+6925C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333584 | |||||||
chr9:134333679 | C | T | 4 | a0001c0001t0005g0004 a0001c0001t0005g0199 a0001c0001t0005g0200 others(1): Show |
4 | NA18939.hp2 NA18955.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+7020C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333679 | |||||||
chr9:134333701 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.28+7042C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333701 | |||||||
chr9:134333883 | C | T | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+7224C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333883 | |||||||
chr9:134333884 | G | A | 1 | a0001c0001t0054g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.28+7225G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134333884 | |||||||
chr9:134334126 | T | C | 116 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(113): Show |
120 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(117): Show |
intron_variant | MODIFIER | c.28+7467T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134334126 | |||||||
chr9:134334174 | C | A | 19 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(16): Show |
21 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.28+7515C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134334174 | |||||||
chr9:134334248 | T | C | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+7589T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134334248 | |||||||
chr9:134334447 | A | T | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+7788A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134334447 | |||||||
chr9:134334590 | C | G | 1 | a0001c0001t0003g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.28+7931C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134334590 | |||||||
chr9:134334845 | G | A | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+8186G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134334845 | |||||||
chr9:134334966 | C | T | 1 | a0001c0001t0008g0125 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.28+8307C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134334966 | |||||||
chr9:134335370 | G | A | 18 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(15): Show |
20 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.28+8711G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134335370 | |||||||
chr9:134335433 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.28+8774C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134335433 | |||||||
chr9:134335441 | A | G | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+8782A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134335441 | |||||||
chr9:134335457 | G | A | 1 | a0001c0001t0010g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28+8798G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134335457 | |||||||
chr9:134335471 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.28+8812G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134335471 | |||||||
chr9:134335478 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.28+8819G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134335478 | |||||||
chr9:134335743 | C | T | 115 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(112): Show |
119 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(116): Show |
intron_variant | MODIFIER | c.28+9084C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134335743 | |||||||
chr9:134335753 | G | T | 1 | a0001c0001t0002g0198 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.28+9094G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134335753 | |||||||
chr9:134335844 | C | A | 2 | a0001c0001t0026g0127 a0001c0004t0005g0126 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28+9185C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134335844 | |||||||
chr9:134335968 | C | T | 4 | a0001c0001t0007g0090 a0001c0001t0008g0087 a0001c0001t0014g0085 others(1): Show |
4 | HG02717.hp2 HG02809.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+9309C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134335968 | |||||||
chr9:134336058 | A | G | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.28+9399A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134336058 | |||||||
chr9:134336097 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.28+9438A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134336097 | |||||||
chr9:134336178 | C | T | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+9519C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134336178 | |||||||
chr9:134336340 | T | C | 28 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(25): Show |
29 | HG00621.hp2 HG00642.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.28+9681T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134336340 | |||||||
chr9:134336399 | T | C | 18 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(15): Show |
20 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.28+9740T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134336399 | |||||||
chr9:134336484 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.28+9825T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134336484 | |||||||
chr9:134336524 | T | C | 113 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(110): Show |
117 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.28+9865T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134336524 | |||||||
chr9:134336553 | G | T | 3 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 |
3 | HG01891.hp2 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.28+9894G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134336553 | |||||||
chr9:134336571 | T | C | 114 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(111): Show |
118 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.28+9912T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134336571 | |||||||
chr9:134336720 | T | C | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0018g0104 others(1): Show |
4 | HG01934.hp2 HG02300.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+10061T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134336720 | |||||||
chr9:134337077 | C | T | 35 | a0001c0001t0001g0194 a0001c0001t0002g0179 a0001c0001t0002g0185 others(32): Show |
36 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.28+10418C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337077 | |||||||
chr9:134337226 | T | G | 13 | a0001c0001t0001g0135 a0001c0001t0004g0128 a0001c0001t0004g0129 others(10): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.28+10567T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337226 | |||||||
chr9:134337312 | T | TCATCTGT others(13): Show |
1 | a0001c0001t0010g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28+10658_28+10677d others(22): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134337312 | ||||||
chr9:134337481 | A | G | 42 | a0001c0001t0001g0194 a0001c0001t0001g0220 a0001c0001t0002g0179 others(39): Show |
43 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.28+10822A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337481 | |||||||
chr9:134337490 | C | T | 1 | a0001c0001t0015g0102 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.28+10831C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337490 | |||||||
chr9:134337526 | T | A | 113 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(110): Show |
117 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.28+10867T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337526 | |||||||
chr9:134337597 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.28+10938G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337597 | |||||||
chr9:134337699 | G | A | 2 | a0001c0001t0009g0098 a0001c0001t0011g0099 |
2 | HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.28+11040G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337699 | |||||||
chr9:134337731 | G | A | 6 | a0001c0001t0001g0220 a0001c0001t0002g0219 a0001c0001t0002g0223 others(3): Show |
6 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.28+11072G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337731 | |||||||
chr9:134337845 | C | T | 1 | a0001c0001t0005g0200 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.28+11186C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337845 | |||||||
chr9:134337903 | G | A | 1 | a0001c0001t0005g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.28+11244G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337903 | |||||||
chr9:134337914 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.28+11255C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337914 | |||||||
chr9:134337916 | C | T | 1 | a0001c0001t0007g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.28+11257C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337916 | |||||||
chr9:134337936 | G | A | 2 | a0001c0001t0003g0142 a0001c0001t0008g0141 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.28+11277G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134337936 | |||||||
chr9:134338009 | C | T | 114 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(111): Show |
118 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.28+11350C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338009 | |||||||
chr9:134338019 | G | T | 1 | a0001c0001t0001g0083 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.28+11360G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338019 | |||||||
chr9:134338141 | A | G | 1 | a0001c0001t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.28+11482A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338141 | |||||||
chr9:134338151 | G | A | 1 | a0001c0001t0006g0021 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.28+11492G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338151 | |||||||
chr9:134338170 | A | G | 113 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(110): Show |
117 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.28+11511A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338170 | |||||||
chr9:134338172 | C | T | 2 | a0001c0001t0026g0127 a0001c0004t0005g0126 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28+11513C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338172 | |||||||
chr9:134338173 | A | G | 113 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(110): Show |
117 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.28+11514A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338173 | |||||||
chr9:134338330 | A | G | 6 | a0001c0001t0001g0220 a0001c0001t0002g0219 a0001c0001t0002g0223 others(3): Show |
6 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.28+11671A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338330 | |||||||
chr9:134338523 | G | A | 36 | a0001c0001t0001g0194 a0001c0001t0002g0179 a0001c0001t0002g0185 others(33): Show |
37 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.28+11864G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338523 | |||||||
chr9:134338532 | C | T | 3 | a0001c0001t0003g0166 a0001c0001t0004g0225 a0001c0001t0005g0165 |
3 | HG01243.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+11873C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338532 | |||||||
chr9:134338627 | G | A | 36 | a0001c0001t0001g0194 a0001c0001t0002g0179 a0001c0001t0002g0185 others(33): Show |
37 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.28+11968G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338627 | |||||||
chr9:134338676 | T | C | 1 | a0001c0001t0005g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.28+12017T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338676 | |||||||
chr9:134338725 | C | T | 113 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(110): Show |
117 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.28+12066C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338725 | |||||||
chr9:134338784 | C | T | 113 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(110): Show |
117 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.28+12125C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338784 | |||||||
chr9:134338802 | C | T | 1 | a0001c0001t0013g0197 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.28+12143C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338802 | |||||||
chr9:134338870 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.28+12211A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338870 | |||||||
chr9:134338944 | C | G | 83 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(80): Show |
85 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.28+12285C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338944 | |||||||
chr9:134338974 | C | G | 1 | a0001c0001t0005g0144 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.28+12315C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134338974 | |||||||
chr9:134339033 | G | A | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+12374G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339033 | |||||||
chr9:134339052 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.28+12393C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339052 | |||||||
chr9:134339110 | C | G | 2 | a0001c0001t0026g0127 a0001c0004t0005g0126 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28+12451C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339110 | |||||||
chr9:134339111 | CT | C | 92 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(89): Show |
94 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.28+12453delT | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339111 | |||||||
chr9:134339112 | T | C | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.28+12453T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339112 | |||||||
chr9:134339124 | C | T | 4 | a0001c0001t0003g0166 a0001c0001t0004g0225 a0001c0001t0005g0165 others(1): Show |
4 | HG01243.hp1 HG02280.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+12465C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339124 | |||||||
chr9:134339125 | G | C | 1 | a0001c0001t0001g0022 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.28+12466G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339125 | |||||||
chr9:134339410 | C | T | 6 | a0001c0001t0001g0220 a0001c0001t0002g0219 a0001c0001t0002g0223 others(3): Show |
6 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.28+12751C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339410 | |||||||
chr9:134339472 | T | C | 3 | a0001c0001t0009g0098 a0001c0001t0011g0099 a0001c0001t0060g0100 |
3 | HG02895.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.28+12813T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339472 | |||||||
chr9:134339498 | T | C | 1 | a0001c0001t0060g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28+12839T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339498 | |||||||
chr9:134339539 | G | A | 113 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(110): Show |
117 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.28+12880G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339539 | |||||||
chr9:134339539 | G | T | 1 | a0001c0001t0003g0080 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.28+12880G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339539 | |||||||
chr9:134339658 | CCTGTGTG others(5): Show |
C | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+13000_28+13011d others(14): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339658 | |||||||
chr9:134339659 | CTGTG | C | 3 | a0001c0001t0004g0195 a0001c0001t0005g0200 a0001c0001t0020g0182 |
3 | HG03453.hp2 NA18522.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.28+13009_28+13012d others(6): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134339659 | ||||||
chr9:134339675 | C | CTG | 7 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(4): Show |
7 | HG00642.hp1 HG01109.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+13030_28+13031d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134339675 | ||||||
chr9:134339675 | CTG | C | 3 | a0001c0001t0009g0130 a0001c0001t0015g0102 a0001c0001t0051g0023 |
3 | HG02723.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.28+13030_28+13031d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134339675 | ||||||
chr9:134339721 | C | CTG | 21 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(18): Show |
23 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.28+13074_28+13075d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134339721 | ||||||
chr9:134339733 | G | C | 1 | a0001c0001t0010g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28+13074G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339733 | |||||||
chr9:134339750 | CGT | C | 18 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(15): Show |
20 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.28+13098_28+13099d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134339750 | ||||||
chr9:134339751 | G | A | 3 | a0001c0001t0005g0147 a0001c0001t0026g0127 a0001c0004t0005g0126 |
3 | HG01891.hp1 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28+13092G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339751 | |||||||
chr9:134339753 | G | A | 18 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(15): Show |
20 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.28+13094G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339753 | |||||||
chr9:134339805 | G | T | 36 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(33): Show |
37 | HG00099.hp2 HG00621.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.28+13146G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339805 | |||||||
chr9:134339810 | A | G | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.28+13151A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339810 | |||||||
chr9:134339815 | C | CTG | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.28+13173_28+13174d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134339815 | ||||||
chr9:134339815 | CTG | C | 51 | a0001c0001t0001g0088 a0001c0001t0001g0194 a0001c0001t0001g0220 others(48): Show |
52 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.28+13173_28+13174d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134339815 | ||||||
chr9:134339837 | CTG | C | 91 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(88): Show |
93 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.28+13189_28+13190d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134339837 | ||||||
chr9:134339864 | T | C | 2 | a0001c0001t0003g0025 a0001c0001t0029g0026 |
2 | NA18947.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.28+13205T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339864 | |||||||
chr9:134339867 | CTG | C | 36 | a0001c0001t0001g0194 a0001c0001t0002g0179 a0001c0001t0002g0185 others(33): Show |
37 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.28+13211_28+13212d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134339867 | ||||||
chr9:134339970 | C | T | 36 | a0001c0001t0001g0194 a0001c0001t0002g0179 a0001c0001t0002g0185 others(33): Show |
37 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.28+13311C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134339970 | |||||||
chr9:134340062 | C | T | 19 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(16): Show |
21 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.28+13403C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340062 | |||||||
chr9:134340099 | G | A | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(1): Show |
4 | HG01928.hp1 HG01978.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+13440G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340099 | |||||||
chr9:134340114 | C | T | 6 | a0001c0001t0001g0220 a0001c0001t0002g0219 a0001c0001t0002g0223 others(3): Show |
6 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.28+13455C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340114 | |||||||
chr9:134340115 | G | A | 23 | a0001c0001t0001g0164 a0001c0001t0001g0217 a0001c0001t0002g0001 others(20): Show |
25 | HG00642.hp1 HG01069.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.28+13456G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340115 | |||||||
chr9:134340184 | T | C | 108 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(105): Show |
112 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.28+13525T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340184 | |||||||
chr9:134340190 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.28+13531C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340190 | |||||||
chr9:134340261 | C | G | 5 | a0001c0001t0003g0142 a0001c0001t0008g0141 a0001c0001t0009g0098 others(2): Show |
5 | HG02145.hp1 HG02895.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+13602C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340261 | |||||||
chr9:134340262 | G | A | 13 | a0001c0001t0001g0135 a0001c0001t0004g0128 a0001c0001t0004g0129 others(10): Show |
13 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.28+13603G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340262 | |||||||
chr9:134340366 | G | A | 1 | a0001c0001t0015g0102 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.28+13707G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340366 | |||||||
chr9:134340512 | G | A | 6 | a0001c0001t0001g0220 a0001c0001t0002g0219 a0001c0001t0002g0223 others(3): Show |
6 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.28+13853G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340512 | |||||||
chr9:134340518 | C | T | 1 | a0001c0001t0003g0224 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.28+13859C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340518 | |||||||
chr9:134340689 | A | G | 88 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(85): Show |
90 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.28+14030A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340689 | |||||||
chr9:134340878 | G | T | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28+14219G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340878 | |||||||
chr9:134340958 | G | A | 1 | a0001c0001t0012g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.28+14299G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134340958 | |||||||
chr9:134341162 | T | G | 6 | a0001c0001t0001g0220 a0001c0001t0002g0219 a0001c0001t0002g0223 others(3): Show |
6 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.28+14503T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134341162 | |||||||
chr9:134341353 | G | T | 3 | a0001c0001t0003g0166 a0001c0001t0004g0225 a0001c0001t0005g0165 |
3 | HG01243.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+14694G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134341353 | |||||||
chr9:134341384 | G | T | 3 | a0001c0001t0009g0098 a0001c0001t0011g0099 a0001c0001t0060g0100 |
3 | HG02895.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.28+14725G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134341384 | |||||||
chr9:134341418 | C | T | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.28+14759C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134341418 | |||||||
chr9:134341433 | T | C | 3 | a0001c0001t0003g0166 a0001c0001t0004g0225 a0001c0001t0005g0165 |
3 | HG01243.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+14774T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134341433 | |||||||
chr9:134341644 | C | A | 1 | a0001c0001t0015g0102 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.28+14985C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134341644 | |||||||
chr9:134341670 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.28+15011C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134341670 | |||||||
chr9:134341875 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.28+15216G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134341875 | |||||||
chr9:134342026 | C | T | 41 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(38): Show |
42 | HG00099.hp2 HG00621.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.28+15367C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342026 | |||||||
chr9:134342079 | C | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.28+15420C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342079 | |||||||
chr9:134342218 | C | T | 19 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(16): Show |
21 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.28+15559C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342218 | |||||||
chr9:134342380 | C | T | 1 | a0001c0001t0010g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28+15721C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342380 | |||||||
chr9:134342419 | C | T | 5 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(2): Show |
5 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+15760C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342419 | |||||||
chr9:134342498 | C | T | 1 | a0001c0001t0011g0140 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.28+15839C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342498 | |||||||
chr9:134342521 | C | G | 98 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(95): Show |
100 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.28+15862C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342521 | |||||||
chr9:134342652 | A | G | 43 | a0001c0001t0001g0194 a0001c0001t0001g0218 a0001c0001t0001g0220 others(40): Show |
44 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.28+15993A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342652 | |||||||
chr9:134342754 | G | A | 1 | a0001c0001t0010g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28+16095G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342754 | |||||||
chr9:134342825 | A | G | 98 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(95): Show |
100 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.28+16166A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342825 | |||||||
chr9:134342933 | T | C | 117 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(114): Show |
121 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(118): Show |
intron_variant | MODIFIER | c.28+16274T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342933 | |||||||
chr9:134342979 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.28+16320C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342979 | |||||||
chr9:134342993 | A | G | 98 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(95): Show |
100 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.28+16334A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134342993 | |||||||
chr9:134343013 | G | T | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+16354G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343013 | |||||||
chr9:134343108 | C | T | 2 | a0001c0001t0026g0127 a0001c0004t0005g0126 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28+16449C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343108 | |||||||
chr9:134343148 | CA | C | 37 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(34): Show |
38 | HG00099.hp2 HG00621.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.28+16490delA | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343148 | |||||||
chr9:134343200 | C | T | 43 | a0001c0001t0001g0194 a0001c0001t0001g0218 a0001c0001t0001g0220 others(40): Show |
44 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.28+16541C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343200 | |||||||
chr9:134343412 | G | A | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.28+16753G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343412 | |||||||
chr9:134343415 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.28+16756C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343415 | |||||||
chr9:134343636 | G | A | 1 | a0001c0001t0010g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28+16977G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343636 | |||||||
chr9:134343665 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.28+17006T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343665 | |||||||
chr9:134343720 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.28+17061G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343720 | |||||||
chr9:134343741 | C | G | 5 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(2): Show |
5 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+17082C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343741 | |||||||
chr9:134343752 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0002g0029 a0001c0001t0006g0021 |
3 | HG01099.hp1 HG01346.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.28+17093G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343752 | |||||||
chr9:134343842 | C | T | 1 | a0001c0001t0011g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28+17183C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343842 | |||||||
chr9:134343881 | C | T | 97 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(94): Show |
99 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.28+17222C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343881 | |||||||
chr9:134343884 | C | G | 97 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(94): Show |
99 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.28+17225C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134343884 | |||||||
chr9:134344007 | C | CG | 37 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(34): Show |
38 | HG00099.hp2 HG00621.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.28+17353dupG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134344007 | ||||||
chr9:134344122 | C | T | 1 | a0001c0001t0015g0102 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.28+17463C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134344122 | |||||||
chr9:134344175 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.28+17516A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134344175 | |||||||
chr9:134344244 | C | G | 19 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0004g0148 others(16): Show |
21 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.28+17585C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134344244 | |||||||
chr9:134344330 | C | A | 1 | a0001c0001t0010g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28+17671C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134344330 | |||||||
chr9:134344372 | G | C | 38 | a0001c0001t0001g0016 a0001c0001t0001g0194 a0001c0001t0002g0031 others(35): Show |
39 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.28+17713G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134344372 | |||||||
chr9:134344378 | G | A | 1 | a0001c0001t0014g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.28+17719G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134344378 | |||||||
chr9:134344481 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.28+17822C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134344481 | |||||||
chr9:134344617 | G | A | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.28+17958G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134344617 | |||||||
chr9:134344675 | G | T | 1 | a0001c0001t0004g0195 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.28+18016G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134344675 | |||||||
chr9:134344698 | C | T | 37 | a0001c0001t0001g0194 a0001c0001t0002g0179 a0001c0001t0002g0185 others(34): Show |
38 | HG00099.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.28+18039C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134344698 | |||||||
chr9:134344859 | C | T | 1 | a0001c0001t0005g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.28+18200C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134344859 | |||||||
chr9:134345090 | C | T | 104 | a0001c0001t0001g0016 a0001c0001t0001g0077 a0001c0001t0001g0103 others(101): Show |
106 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(103): Show |
intron_variant | MODIFIER | c.28+18431C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134345090 | |||||||
chr9:134345093 | G | A | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+18434G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134345093 | |||||||
chr9:134345101 | C | G | 16 | a0001c0001t0001g0077 a0001c0001t0001g0164 a0001c0001t0001g0175 others(13): Show |
16 | HG00099.hp2 HG01943.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.28+18442C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134345101 | |||||||
chr9:134345144 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.28+18485C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134345144 | |||||||
chr9:134345449 | T | A | 131 | a0001c0001t0001g0016 a0001c0001t0001g0077 a0001c0001t0001g0103 others(128): Show |
135 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(132): Show |
intron_variant | MODIFIER | c.28+18790T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134345449 | |||||||
chr9:134345529 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0036g0201 |
2 | HG00642.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.28+18870C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134345529 | |||||||
chr9:134345548 | C | T | 4 | a0001c0001t0015g0114 a0001c0001t0016g0115 a0001c0001t0047g0116 others(1): Show |
4 | HG02886.hp2 NA18906.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+18889C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134345548 | |||||||
chr9:134345653 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0002g0081 |
2 | HG01099.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.28+18994A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134345653 | |||||||
chr9:134345815 | C | T | 102 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(99): Show |
104 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.28+19156C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134345815 | |||||||
chr9:134345836 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.28+19177C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134345836 | |||||||
chr9:134345946 | A | G | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+19287A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134345946 | |||||||
chr9:134346099 | T | C | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.28+19440T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346099 | |||||||
chr9:134346112 | C | T | 16 | a0001c0001t0001g0077 a0001c0001t0001g0164 a0001c0001t0001g0175 others(13): Show |
16 | HG00099.hp2 HG01943.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.28+19453C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346112 | |||||||
chr9:134346120 | C | T | 1 | a0001c0001t0009g0130 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.28+19461C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346120 | |||||||
chr9:134346124 | C | T | 1 | a0001c0001t0010g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28+19465C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346124 | |||||||
chr9:134346199 | C | T | 2 | a0001c0001t0003g0073 a0001c0001t0005g0020 |
2 | HG01192.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.28+19540C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346199 | |||||||
chr9:134346256 | C | T | 45 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(42): Show |
46 | HG00099.hp2 HG00621.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.28+19597C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346256 | |||||||
chr9:134346367 | G | A | 5 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(2): Show |
5 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+19708G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346367 | |||||||
chr9:134346450 | G | T | 5 | a0001c0001t0001g0164 a0001c0001t0004g0148 a0001c0001t0010g0163 others(2): Show |
5 | HG01943.hp2 HG02109.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+19791G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346450 | |||||||
chr9:134346468 | G | C | 1 | a0001c0001t0004g0225 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.28+19809G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346468 | |||||||
chr9:134346518 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.28+19859C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346518 | |||||||
chr9:134346649 | C | T | 27 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(24): Show |
28 | HG00621.hp2 HG00733.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.28+19990C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346649 | |||||||
chr9:134346724 | C | T | 2 | a0001c0001t0003g0142 a0001c0001t0008g0141 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.28+20065C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346724 | |||||||
chr9:134346745 | T | A | 105 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0077 others(102): Show |
107 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.28+20086T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346745 | |||||||
chr9:134346780 | A | C | 46 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0194 others(43): Show |
47 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.28+20121A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134346780 | |||||||
chr9:134347117 | C | G | 47 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(44): Show |
48 | HG00099.hp2 HG00621.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.28+20458C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134347117 | |||||||
chr9:134347317 | A | G | 105 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0077 others(102): Show |
107 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.28+20658A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134347317 | |||||||
chr9:134347329 | C | G | 15 | a0001c0001t0002g0001 a0001c0001t0004g0153 a0001c0001t0004g0160 others(12): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.28+20670C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134347329 | |||||||
chr9:134347352 | A | G | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+20693A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134347352 | |||||||
chr9:134347443 | G | A | 1 | a0001c0001t0030g0033 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.28+20784G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134347443 | |||||||
chr9:134347543 | G | A | 1 | a0001c0001t0003g0080 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.28+20884G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134347543 | |||||||
chr9:134347664 | G | A | 2 | a0001c0001t0003g0142 a0001c0001t0008g0141 |
2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.28+21005G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134347664 | |||||||
chr9:134347760 | T | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.28+21101T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134347760 | |||||||
chr9:134347930 | G | A | 1 | a0001c0003t0013g0034 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.28+21271G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134347930 | |||||||
chr9:134347964 | C | T | 105 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0077 others(102): Show |
107 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.28+21305C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134347964 | |||||||
chr9:134348065 | C | T | 105 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0077 others(102): Show |
107 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.28+21406C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134348065 | |||||||
chr9:134348068 | G | C | 1 | a0001c0001t0002g0226 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.28+21409G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134348068 | |||||||
chr9:134348072 | G | C | 1 | a0001c0001t0002g0226 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.28+21413G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134348072 | |||||||
chr9:134348282 | T | C | 49 | a0001c0001t0001g0077 a0001c0001t0001g0103 a0001c0001t0001g0107 others(46): Show |
50 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.28+21623T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134348282 | |||||||
chr9:134348513 | TGG | T | 105 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0077 others(102): Show |
107 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.28+21857_28+21858d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134348513 | ||||||
chr9:134348568 | C | T | 1 | a0001c0001t0014g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.28+21909C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134348568 | |||||||
chr9:134348687 | CG | C | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+22032delG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134348687 | ||||||
chr9:134348795 | T | TCATGTAC others(4): Show |
10 | a0001c0001t0001g0077 a0001c0001t0001g0175 a0001c0001t0001g0178 others(7): Show |
10 | HG00099.hp2 HG03492.hp1 HG03927.hp1 others(7): Show |
intron_variant | MODIFIER | c.28+22137_28+22138i others(13): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134348795 | ||||||
chr9:134348795 | T | TCATGTGC others(4): Show |
122 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0103 others(119): Show |
126 | HG00597.hp2 HG00621.hp2 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.28+22137_28+22138i others(13): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134348795 | ||||||
chr9:134349006 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.28+22347G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134349006 | |||||||
chr9:134349087 | G | A | 105 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0077 others(102): Show |
107 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.28+22428G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134349087 | |||||||
chr9:134349174 | G | T | 58 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0194 others(55): Show |
59 | HG00597.hp2 HG00642.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.28+22515G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134349174 | |||||||
chr9:134349284 | C | G | 3 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 |
3 | HG01891.hp2 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.28+22625C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134349284 | |||||||
chr9:134349304 | C | T | 48 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0194 others(45): Show |
49 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.28+22645C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134349304 | |||||||
chr9:134349433 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.28+22774C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134349433 | |||||||
chr9:134349638 | A | G | 11 | a0001c0001t0001g0077 a0001c0001t0001g0175 a0001c0001t0001g0178 others(8): Show |
11 | HG00099.hp2 HG02717.hp1 HG03492.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+22979A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134349638 | |||||||
chr9:134349687 | G | A | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28+23028G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134349687 | |||||||
chr9:134349710 | C | T | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+23051C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134349710 | |||||||
chr9:134349838 | C | A | 2 | a0001c0001t0003g0166 a0001c0001t0005g0165 |
2 | HG01243.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+23179C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134349838 | |||||||
chr9:134349966 | G | GCTGGGAC others(13): Show |
1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28+23309_28+23328d others(22): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134349966 | ||||||
chr9:134350075 | TA | T | 2 | a0001c0001t0009g0098 a0001c0001t0011g0099 |
2 | HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.28+23417delA | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134350075 | |||||||
chr9:134350083 | G | C | 1 | a0001c0001t0003g0025 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.28+23424G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134350083 | |||||||
chr9:134350136 | C | T | 1 | a0001c0001t0002g0001 | 3 | HG01069.hp1 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.28+23477C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134350136 | |||||||
chr9:134350392 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.28+23733C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134350392 | |||||||
chr9:134350443 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.28+23784C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134350443 | |||||||
chr9:134350677 | C | T | 2 | a0001c0001t0026g0127 a0001c0004t0005g0126 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28+24018C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134350677 | |||||||
chr9:134350816 | C | T | 1 | a0001c0001t0004g0225 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.28+24157C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134350816 | |||||||
chr9:134350828 | C | T | 1 | a0001c0001t0004g0225 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.28+24169C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134350828 | |||||||
chr9:134350844 | C | T | 39 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0194 others(36): Show |
40 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.28+24185C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134350844 | |||||||
chr9:134350852 | C | A | 16 | a0001c0001t0001g0077 a0001c0001t0001g0164 a0001c0001t0001g0175 others(13): Show |
16 | HG00099.hp2 HG01943.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.28+24193C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134350852 | |||||||
chr9:134350918 | T | C | 98 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0077 others(95): Show |
101 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.28+24259T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134350918 | |||||||
chr9:134351238 | A | C | 1 | a0001c0001t0012g0162 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.28+24579A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134351238 | |||||||
chr9:134351302 | G | A | 23 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0112 others(20): Show |
24 | HG00621.hp2 HG00733.hp2 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.28+24643G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134351302 | |||||||
chr9:134351305 | G | C | 1 | a0001c0001t0007g0035 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.28+24646G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134351305 | |||||||
chr9:134351372 | C | T | 13 | a0001c0001t0002g0001 a0001c0001t0004g0153 a0001c0001t0004g0160 others(10): Show |
15 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.28+24713C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134351372 | |||||||
chr9:134351489 | G | C | 1 | a0001c0001t0001g0178 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.28+24830G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134351489 | |||||||
chr9:134351537 | C | T | 51 | a0001c0001t0001g0016 a0001c0001t0001g0194 a0001c0001t0001g0218 others(48): Show |
52 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.28+24878C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134351537 | |||||||
chr9:134351544 | G | A | 12 | a0001c0001t0004g0005 a0001c0001t0004g0202 a0001c0001t0004g0204 others(9): Show |
13 | HG00735.hp2 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.28+24885G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134351544 | |||||||
chr9:134351636 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.28+24977T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134351636 | |||||||
chr9:134351832 | G | A | 2 | a0001c0001t0008g0037 a0001c0001t0012g0038 |
2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.28+25173G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134351832 | |||||||
chr9:134351849 | C | A | 2 | a0001c0001t0006g0039 a0001c0002t0040g0040 |
2 | HG01255.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.28+25190C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134351849 | |||||||
chr9:134352040 | G | A | 1 | a0001c0001t0011g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28+25381G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352040 | |||||||
chr9:134352046 | G | T | 1 | a0001c0001t0002g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.28+25387G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352046 | |||||||
chr9:134352082 | C | T | 22 | a0001c0001t0001g0077 a0001c0001t0001g0164 a0001c0001t0001g0175 others(19): Show |
22 | HG00099.hp2 HG01943.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.28+25423C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352082 | |||||||
chr9:134352272 | A | G | 14 | a0001c0001t0002g0001 a0001c0001t0004g0153 a0001c0001t0004g0160 others(11): Show |
16 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.28+25613A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352272 | |||||||
chr9:134352322 | G | A | 13 | a0001c0001t0002g0001 a0001c0001t0004g0153 a0001c0001t0004g0160 others(10): Show |
15 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.28+25663G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352322 | |||||||
chr9:134352356 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.28+25697G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352356 | |||||||
chr9:134352431 | G | A | 3 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 |
3 | HG01891.hp2 HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.28+25772G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352431 | |||||||
chr9:134352436 | A | C | 7 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0002g0219 others(4): Show |
7 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+25777A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352436 | |||||||
chr9:134352475 | C | T | 1 | a0001c0001t0002g0226 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.28+25816C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352475 | |||||||
chr9:134352540 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0021g0106 |
3 | HG01074.hp2 HG01346.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.28+25881G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352540 | |||||||
chr9:134352600 | T | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0015g0168 |
3 | HG02451.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.28+25941T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352600 | |||||||
chr9:134352739 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.28+26080G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352739 | |||||||
chr9:134352846 | T | C | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+26187T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352846 | |||||||
chr9:134352848 | G | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0083 |
3 | NA18944.hp1 NA18954.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.28+26189G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134352848 | |||||||
chr9:134353036 | G | A | 1 | a0001c0001t0007g0035 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.28+26377G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134353036 | |||||||
chr9:134353071 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.28+26412C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134353071 | |||||||
chr9:134353188 | C | G | 14 | a0001c0001t0002g0001 a0001c0001t0004g0153 a0001c0001t0004g0160 others(11): Show |
16 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.28+26529C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134353188 | |||||||
chr9:134353282 | G | A | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28+26623G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134353282 | |||||||
chr9:134353350 | A | G | 1 | a0001c0001t0003g0166 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.28+26691A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134353350 | |||||||
chr9:134353433 | C | T | 1 | a0001c0001t0041g0139 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.28+26774C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134353433 | |||||||
chr9:134353586 | T | C | 1 | a0001c0001t0002g0219 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.28+26927T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134353586 | |||||||
chr9:134353685 | C | G | 14 | a0001c0001t0002g0001 a0001c0001t0004g0153 a0001c0001t0004g0160 others(11): Show |
16 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.28+27026C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134353685 | |||||||
chr9:134353687 | T | C | 99 | a0001c0001t0001g0016 a0001c0001t0001g0077 a0001c0001t0001g0164 others(96): Show |
102 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.28+27028T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134353687 | |||||||
chr9:134354031 | C | T | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+27372C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134354031 | |||||||
chr9:134354067 | C | G | 4 | a0001c0001t0009g0098 a0001c0001t0010g0101 a0001c0001t0011g0099 others(1): Show |
4 | HG02258.hp1 HG02895.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+27408C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134354067 | |||||||
chr9:134354072 | A | G | 14 | a0001c0001t0002g0001 a0001c0001t0004g0153 a0001c0001t0004g0160 others(11): Show |
16 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.28+27413A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134354072 | |||||||
chr9:134354127 | C | T | 3 | a0001c0001t0003g0166 a0001c0001t0004g0225 a0001c0001t0005g0165 |
3 | HG01243.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+27468C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134354127 | |||||||
chr9:134354221 | C | T | 1 | a0001c0001t0062g0120 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.28+27562C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134354221 | |||||||
chr9:134354224 | C | T | 4 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(1): Show |
4 | HG00642.hp1 HG01109.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+27565C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134354224 | |||||||
chr9:134354287 | C | T | 1 | a0001c0001t0007g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.28+27628C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134354287 | |||||||
chr9:134354416 | T | C | 13 | a0001c0001t0002g0001 a0001c0001t0004g0153 a0001c0001t0004g0160 others(10): Show |
15 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.28+27757T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134354416 | |||||||
chr9:134354418 | G | A | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28+27759G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134354418 | |||||||
chr9:134354754 | C | T | 11 | a0001c0001t0001g0135 a0001c0001t0004g0128 a0001c0001t0004g0129 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.28+28095C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134354754 | |||||||
chr9:134354899 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.28+28240T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134354899 | |||||||
chr9:134355051 | A | G | 27 | a0001c0001t0001g0077 a0001c0001t0001g0164 a0001c0001t0001g0175 others(24): Show |
27 | HG00099.hp2 HG01891.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.28+28392A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134355051 | |||||||
chr9:134355172 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.28+28513C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134355172 | |||||||
chr9:134355368 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.28+28709C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134355368 | |||||||
chr9:134355497 | T | C | 1 | a0001c0001t0049g0041 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.28+28838T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134355497 | |||||||
chr9:134355500 | C | A | 69 | a0001c0001t0001g0016 a0001c0001t0001g0194 a0001c0001t0001g0217 others(66): Show |
72 | HG00597.hp2 HG00642.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.28+28841C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134355500 | |||||||
chr9:134355557 | T | C | 107 | a0001c0001t0001g0016 a0001c0001t0001g0077 a0001c0001t0001g0135 others(104): Show |
110 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.28+28898T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134355557 | |||||||
chr9:134355656 | G | C | 1 | a0001c0001t0033g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28+28997G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134355656 | |||||||
chr9:134355800 | G | C | 2 | a0001c0001t0026g0127 a0001c0004t0005g0126 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28+29141G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134355800 | |||||||
chr9:134355804 | A | G | 7 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0002g0219 others(4): Show |
7 | HG00738.hp2 HG01070.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.28+29145A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134355804 | |||||||
chr9:134355948 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.28+29289G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134355948 | |||||||
chr9:134355991 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.28+29332C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134355991 | |||||||
chr9:134356257 | C | A | 15 | a0001c0001t0002g0001 a0001c0001t0004g0153 a0001c0001t0004g0160 others(12): Show |
17 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.28+29598C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134356257 | |||||||
chr9:134356275 | G | A | 2 | a0001c0001t0026g0127 a0001c0004t0005g0126 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28+29616G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134356275 | |||||||
chr9:134356320 | T | C | 99 | a0001c0001t0001g0016 a0001c0001t0001g0077 a0001c0001t0001g0164 others(96): Show |
102 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(99): Show |
intron_variant | MODIFIER | c.28+29661T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134356320 | |||||||
chr9:134356434 | G | A | 1 | a0001c0001t0002g0029 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.28+29775G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134356434 | |||||||
chr9:134356436 | G | T | 47 | a0001c0001t0001g0016 a0001c0001t0001g0194 a0001c0001t0001g0220 others(44): Show |
48 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.28+29777G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134356436 | |||||||
chr9:134356574 | G | T | 1 | a0001c0001t0005g0200 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.28+29915G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134356574 | |||||||
chr9:134356828 | T | C | 110 | a0001c0001t0001g0016 a0001c0001t0001g0077 a0001c0001t0001g0135 others(107): Show |
113 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.28+30169T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134356828 | |||||||
chr9:134356912 | C | T | 6 | a0001c0001t0001g0164 a0001c0001t0004g0148 a0001c0001t0010g0163 others(3): Show |
6 | HG01943.hp2 HG02109.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.28+30253C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134356912 | |||||||
chr9:134356937 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.28+30278G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134356937 | |||||||
chr9:134357017 | G | A | 2 | a0001c0001t0018g0104 a0001c0001t0018g0105 |
2 | NA18944.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.28+30358G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134357017 | |||||||
chr9:134357079 | C | G | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.28+30420C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134357079 | |||||||
chr9:134357212 | T | C | 42 | a0001c0001t0001g0077 a0001c0001t0001g0164 a0001c0001t0001g0175 others(39): Show |
44 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.28+30553T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134357212 | |||||||
chr9:134357392 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.28+30733C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134357392 | |||||||
chr9:134357420 | G | C | 3 | a0001c0001t0003g0166 a0001c0001t0004g0225 a0001c0001t0005g0165 |
3 | HG01243.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+30761G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134357420 | |||||||
chr9:134357432 | G | A | 1 | a0001c0001t0004g0128 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.28+30773G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134357432 | |||||||
chr9:134357692 | A | G | 3 | a0001c0001t0003g0142 a0001c0001t0008g0131 a0001c0001t0041g0139 |
3 | HG02145.hp1 HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.28+31033A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134357692 | |||||||
chr9:134357770 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0066 others(4): Show |
8 | HG00423.hp2 HG02293.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.28+31111C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134357770 | |||||||
chr9:134357773 | G | A | 5 | a0001c0001t0003g0142 a0001c0001t0007g0108 a0001c0001t0008g0131 others(2): Show |
5 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+31114G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134357773 | |||||||
chr9:134357898 | C | T | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28+31239C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134357898 | |||||||
chr9:134357930 | A | AGAG | 3 | a0001c0001t0007g0119 a0001c0001t0026g0127 a0001c0004t0005g0126 |
3 | HG02976.hp2 HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.28+31291_28+31293d others(5): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134357930 | ||||||
chr9:134357930 | AGAG | A | 6 | a0001c0001t0004g0205 a0001c0001t0004g0209 a0001c0001t0010g0213 others(3): Show |
6 | HG02257.hp2 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.28+31291_28+31293d others(5): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134357930 | ||||||
chr9:134357974 | G | A | 1 | a0001c0001t0007g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.28+31315G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134357974 | |||||||
chr9:134358153 | G | A | 2 | a0001c0001t0004g0202 a0001c0001t0007g0203 |
2 | HG00735.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.28+31494G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134358153 | |||||||
chr9:134358292 | C | T | 1 | a0001c0001t0010g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28+31633C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134358292 | |||||||
chr9:134358306 | A | AGCAG | 2 | a0001c0001t0026g0127 a0001c0004t0005g0126 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.28+31669_28+31672d others(6): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134358306 | ||||||
chr9:134358306 | AGCAG | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0015g0168 |
3 | HG02451.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.28+31669_28+31672d others(6): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134358306 | ||||||
chr9:134358306 | AGCAGGCA others(1): Show |
A | 3 | a0001c0001t0003g0166 a0001c0001t0004g0225 a0001c0001t0005g0165 |
3 | HG01243.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+31665_28+31672d others(10): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134358306 | ||||||
chr9:134358444 | C | T | 1 | a0001c0001t0004g0195 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.28+31785C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134358444 | |||||||
chr9:134358639 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.28+31980A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134358639 | |||||||
chr9:134358693 | C | T | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.28+32034C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134358693 | |||||||
chr9:134358711 | C | G | 1 | a0001c0001t0032g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.28+32052C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134358711 | |||||||
chr9:134358805 | C | T | 5 | a0001c0001t0003g0142 a0001c0001t0007g0108 a0001c0001t0008g0131 others(2): Show |
5 | HG02145.hp1 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+32146C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134358805 | |||||||
chr9:134358879 | G | A | 6 | a0001c0001t0008g0125 a0001c0001t0009g0098 a0001c0001t0010g0122 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.28+32220G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134358879 | |||||||
chr9:134358965 | C | A | 1 | a0001c0001t0004g0195 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.28+32306C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134358965 | |||||||
chr9:134359026 | G | T | 3 | a0001c0001t0003g0166 a0001c0001t0004g0225 a0001c0001t0005g0165 |
3 | HG01243.hp1 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.28+32367G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134359026 | |||||||
chr9:134359089 | C | T | 1 | a0001c0001t0005g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.28+32430C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134359089 | |||||||
chr9:134359307 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.28+32648G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134359307 | |||||||
chr9:134359624 | G | T | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.28+32965G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134359624 | |||||||
chr9:134359704 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0068 others(1): Show |
5 | HG00423.hp2 NA18944.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+33045C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134359704 | |||||||
chr9:134359782 | CCT | C | 27 | a0001c0001t0001g0135 a0001c0001t0001g0170 a0001c0001t0002g0001 others(24): Show |
29 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.28+33124_28+33125d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134359782 | |||||||
chr9:134359827 | C | T | 1 | a0001c0001t0031g0065 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.28+33168C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134359827 | |||||||
chr9:134359856 | C | T | 27 | a0001c0001t0001g0077 a0001c0001t0001g0175 a0001c0001t0001g0178 others(24): Show |
29 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.28+33197C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134359856 | |||||||
chr9:134359879 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.28+33220C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134359879 | |||||||
chr9:134360016 | C | T | 1 | a0001c0001t0045g0161 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.28+33357C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360016 | |||||||
chr9:134360102 | G | A | 2 | a0001c0001t0003g0009 a0001c0001t0003g0010 |
2 | HG00642.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.28+33443G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360102 | |||||||
chr9:134360105 | G | A | 1 | a0001c0001t0003g0073 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.28+33446G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360105 | |||||||
chr9:134360106 | A | T | 2 | a0001c0001t0003g0073 a0001c0001t0005g0020 |
2 | HG01192.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.28+33447A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360106 | |||||||
chr9:134360209 | A | T | 1 | a0001c0001t0005g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.28+33550A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360209 | |||||||
chr9:134360498 | A | G | 2 | a0001c0001t0006g0181 a0001c0001t0014g0180 |
2 | HG01256.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.28+33839A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360498 | |||||||
chr9:134360527 | A | G | 1 | a0001c0001t0011g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28+33868A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360527 | |||||||
chr9:134360533 | C | T | 51 | a0001c0001t0001g0077 a0001c0001t0001g0135 a0001c0001t0001g0164 others(48): Show |
53 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.28+33874C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360533 | |||||||
chr9:134360549 | C | T | 51 | a0001c0001t0001g0077 a0001c0001t0001g0135 a0001c0001t0001g0164 others(48): Show |
53 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.28+33890C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360549 | |||||||
chr9:134360590 | C | T | 1 | a0001c0001t0005g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.28+33931C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360590 | |||||||
chr9:134360655 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.28+33996A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360655 | |||||||
chr9:134360914 | C | T | 57 | a0001c0001t0001g0016 a0001c0001t0001g0194 a0001c0001t0001g0218 others(54): Show |
58 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.28+34255C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360914 | |||||||
chr9:134360940 | G | C | 109 | a0001c0001t0001g0016 a0001c0001t0001g0077 a0001c0001t0001g0135 others(106): Show |
112 | HG00099.hp2 HG00597.hp2 HG00642.hp1 others(109): Show |
intron_variant | MODIFIER | c.28+34281G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134360940 | |||||||
chr9:134361274 | G | A | 1 | a0001c0001t0060g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28+34615G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134361274 | |||||||
chr9:134361450 | C | T | 2 | a0001c0001t0003g0025 a0001c0001t0029g0026 |
2 | NA18947.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.28+34791C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134361450 | |||||||
chr9:134361575 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.28+34916C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134361575 | |||||||
chr9:134361601 | G | A | 52 | a0001c0001t0001g0077 a0001c0001t0001g0135 a0001c0001t0001g0164 others(49): Show |
54 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.28+34942G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134361601 | |||||||
chr9:134361822 | C | T | 1 | a0001c0001t0009g0098 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.28+35163C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134361822 | |||||||
chr9:134361823 | G | T | 39 | a0001c0001t0001g0016 a0001c0001t0001g0194 a0001c0001t0002g0031 others(36): Show |
40 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.28+35164G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134361823 | |||||||
chr9:134362171 | C | T | 70 | a0001c0001t0001g0016 a0001c0001t0001g0194 a0001c0001t0001g0217 others(67): Show |
73 | HG00597.hp2 HG00642.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.28+35512C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134362171 | |||||||
chr9:134362172 | G | A | 19 | a0001c0001t0001g0077 a0001c0001t0001g0175 a0001c0001t0001g0178 others(16): Show |
19 | HG00099.hp2 HG01891.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.28+35513G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134362172 | |||||||
chr9:134362378 | G | A | 5 | a0001c0001t0002g0097 a0001c0001t0003g0043 a0001c0001t0003g0044 others(2): Show |
5 | NA18939.hp1 NA18954.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+35719G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134362378 | |||||||
chr9:134362398 | A | G | 2 | a0001c0001t0004g0225 a0001c0001t0056g0143 |
2 | HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.28+35739A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134362398 | |||||||
chr9:134362914 | C | A | 1 | a0001c0001t0005g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.28+36255C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134362914 | |||||||
chr9:134362943 | C | T | 1 | a0001c0001t0002g0031 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.28+36284C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134362943 | |||||||
chr9:134363118 | G | C | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.28+36459G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363118 | |||||||
chr9:134363298 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.28+36639C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363298 | |||||||
chr9:134363323 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.28+36664C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363323 | |||||||
chr9:134363357 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.28+36698C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363357 | |||||||
chr9:134363373 | C | T | 1 | a0001c0001t0005g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.28+36714C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363373 | |||||||
chr9:134363411 | T | C | 1 | a0001c0001t0007g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.28+36752T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363411 | |||||||
chr9:134363535 | C | T | 4 | a0001c0001t0005g0147 a0001c0001t0008g0087 a0001c0001t0026g0127 others(1): Show |
4 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+36876C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363535 | |||||||
chr9:134363573 | C | T | 3 | a0001c0001t0005g0165 a0001c0001t0008g0131 a0001c0001t0041g0139 |
3 | HG02723.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.28+36914C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363573 | |||||||
chr9:134363593 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.28+36934C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363593 | |||||||
chr9:134363653 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.28+36994C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363653 | |||||||
chr9:134363780 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.28+37121C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363780 | |||||||
chr9:134363787 | G | A | 1 | a0001c0001t0052g0012 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.28+37128G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363787 | |||||||
chr9:134363968 | T | C | 4 | a0001c0001t0005g0147 a0001c0001t0008g0087 a0001c0001t0026g0127 others(1): Show |
4 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+37309T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134363968 | |||||||
chr9:134364005 | C | T | 4 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+37346C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134364005 | |||||||
chr9:134364232 | G | A | 121 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(118): Show |
125 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(122): Show |
intron_variant | MODIFIER | c.29-37400G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134364232 | |||||||
chr9:134364547 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.29-37085C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134364547 | |||||||
chr9:134364554 | G | A | 4 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-37078G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134364554 | |||||||
chr9:134364558 | A | G | 59 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(56): Show |
61 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.29-37074A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134364558 | |||||||
chr9:134364802 | C | T | 1 | a0001c0001t0032g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.29-36830C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134364802 | |||||||
chr9:134364841 | G | C | 1 | a0001c0002t0040g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.29-36791G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134364841 | |||||||
chr9:134364853 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.29-36779C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134364853 | |||||||
chr9:134365054 | A | T | 1 | a0001c0001t0011g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.29-36578A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365054 | |||||||
chr9:134365089 | C | T | 1 | a0001c0001t0004g0160 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.29-36543C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365089 | |||||||
chr9:134365091 | G | C | 1 | a0001c0001t0016g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.29-36541G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365091 | |||||||
chr9:134365140 | A | G | 2 | a0001c0001t0008g0141 a0001c0001t0056g0143 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.29-36492A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365140 | |||||||
chr9:134365319 | C | T | 26 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0118 others(23): Show |
28 | HG00621.hp2 HG00733.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.29-36313C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365319 | |||||||
chr9:134365396 | G | C | 1 | a0001c0001t0004g0160 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.29-36236G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365396 | |||||||
chr9:134365433 | G | C | 14 | a0001c0001t0002g0001 a0001c0001t0004g0205 a0001c0001t0005g0165 others(11): Show |
16 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.29-36199G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365433 | |||||||
chr9:134365444 | G | A | 2 | a0001c0001t0006g0181 a0001c0001t0014g0180 |
2 | HG01256.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.29-36188G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365444 | |||||||
chr9:134365457 | G | A | 1 | a0001c0001t0020g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-36175G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365457 | |||||||
chr9:134365499 | T | C | 1 | a0001c0001t0005g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.29-36133T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365499 | |||||||
chr9:134365597 | T | C | 36 | a0001c0001t0001g0046 a0001c0001t0001g0194 a0001c0001t0001g0218 others(33): Show |
36 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.29-36035T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365597 | |||||||
chr9:134365744 | C | A | 9 | a0001c0001t0002g0001 a0001c0001t0004g0205 a0001c0001t0009g0157 others(6): Show |
11 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.29-35888C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365744 | |||||||
chr9:134365810 | C | T | 24 | a0001c0001t0001g0135 a0001c0001t0001g0164 a0001c0001t0003g0166 others(21): Show |
24 | HG01243.hp1 HG01943.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.29-35822C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365810 | |||||||
chr9:134365813 | A | G | 2 | a0001c0001t0008g0141 a0001c0001t0056g0143 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.29-35819A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134365813 | |||||||
chr9:134366011 | G | C | 1 | a0001c0001t0008g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.29-35621G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134366011 | |||||||
chr9:134366085 | G | A | 1 | a0001c0001t0003g0174 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.29-35547G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134366085 | |||||||
chr9:134366171 | G | A | 1 | a0001c0001t0008g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.29-35461G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134366171 | |||||||
chr9:134366194 | G | A | 2 | a0001c0001t0008g0141 a0001c0001t0056g0143 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.29-35438G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134366194 | |||||||
chr9:134366215 | G | T | 4 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-35417G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134366215 | |||||||
chr9:134366507 | C | T | 1 | a0001c0005t0001g0193 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.29-35125C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134366507 | |||||||
chr9:134366526 | C | T | 2 | a0001c0001t0008g0141 a0001c0001t0056g0143 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.29-35106C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134366526 | |||||||
chr9:134366656 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.29-34976G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134366656 | |||||||
chr9:134366780 | C | T | 1 | a0001c0001t0016g0115 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.29-34852C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134366780 | |||||||
chr9:134366849 | G | A | 7 | a0001c0001t0004g0005 a0001c0001t0004g0153 a0001c0001t0004g0204 others(4): Show |
8 | HG02257.hp2 HG02486.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.29-34783G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134366849 | |||||||
chr9:134366938 | G | A | 1 | a0001c0001t0004g0209 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.29-34694G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134366938 | |||||||
chr9:134366966 | C | G | 11 | a0001c0001t0001g0164 a0001c0001t0004g0148 a0001c0001t0009g0098 others(8): Show |
11 | HG01943.hp2 HG02109.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.29-34666C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134366966 | |||||||
chr9:134367112 | G | A | 23 | a0001c0001t0001g0135 a0001c0001t0001g0164 a0001c0001t0003g0166 others(20): Show |
23 | HG01243.hp1 HG01943.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.29-34520G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134367112 | |||||||
chr9:134367118 | A | G | 2 | a0001c0001t0004g0204 a0001c0001t0022g0208 |
2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.29-34514A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134367118 | |||||||
chr9:134367302 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.29-34330C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134367302 | |||||||
chr9:134367328 | G | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.29-34304G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134367328 | |||||||
chr9:134367328 | G | T | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.29-34304G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134367328 | |||||||
chr9:134367437 | T | C | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.29-34195T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134367437 | |||||||
chr9:134367533 | C | T | 2 | a0001c0001t0008g0141 a0001c0001t0056g0143 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.29-34099C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134367533 | |||||||
chr9:134367547 | T | G | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.29-34085T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134367547 | |||||||
chr9:134367684 | G | T | 1 | a0001c0001t0020g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-33948G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134367684 | |||||||
chr9:134367777 | C | A | 1 | a0001c0001t0001g0036 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.29-33855C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134367777 | |||||||
chr9:134368146 | T | C | 89 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(86): Show |
93 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.29-33486T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368146 | |||||||
chr9:134368235 | C | T | 1 | a0001c0001t0004g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.29-33397C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368235 | |||||||
chr9:134368402 | C | A | 1 | a0001c0001t0004g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.29-33230C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368402 | |||||||
chr9:134368404 | G | A | 3 | a0001c0001t0004g0133 a0001c0001t0007g0119 a0001c0001t0007g0203 |
3 | HG02258.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.29-33228G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368404 | |||||||
chr9:134368457 | C | G | 5 | a0001c0001t0004g0160 a0001c0001t0005g0147 a0001c0001t0008g0087 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-33175C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368457 | |||||||
chr9:134368507 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.29-33125G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368507 | |||||||
chr9:134368576 | G | A | 2 | a0001c0001t0005g0004 a0001c0001t0043g0004 |
2 | NA18955.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.29-33056G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368576 | |||||||
chr9:134368756 | G | T | 1 | a0001c0001t0059g0210 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.29-32876G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368756 | |||||||
chr9:134368766 | C | CTA | 121 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(118): Show |
125 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(122): Show |
intron_variant | MODIFIER | c.29-32865_29-32864i others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368766 | ||||||
chr9:134368840 | A | G | 2 | a0001c0001t0008g0131 a0001c0001t0041g0139 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.29-32792A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368840 | |||||||
chr9:134368875 | A | ATGTGTGT others(14): Show |
4 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-32749_29-32748i others(23): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368875 | ||||||
chr9:134368889 | A | G | 4 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-32743A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368889 | |||||||
chr9:134368896 | A | ATGTATGT others(130): Show |
4 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-32733_29-32732i others(139): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368896 | ||||||
chr9:134368896 | A | G | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.29-32736A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368896 | |||||||
chr9:134368900 | GTGTGTGG others(35): Show |
G | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.29-32725_29-32684d others(44): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368900 | ||||||
chr9:134368913 | G | A | 4 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-32719G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368913 | |||||||
chr9:134368917 | GTGTGTGT others(18): Show |
G | 1 | a0001c0001t0010g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.29-32694_29-32670d others(27): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368917 | ||||||
chr9:134368931 | G | A | 62 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(59): Show |
64 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.29-32701G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368931 | |||||||
chr9:134368931 | G | C | 4 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-32701G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368931 | |||||||
chr9:134368938 | A | G | 10 | a0001c0001t0002g0001 a0001c0001t0004g0205 a0001c0001t0009g0157 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.29-32694A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368938 | |||||||
chr9:134368940 | G | GTGTGTGG others(3): Show |
1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-32691_29-32690i others(12): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368940 | ||||||
chr9:134368940 | G | GTGTGTGG others(142): Show |
5 | a0001c0001t0004g0205 a0001c0001t0012g0151 a0001c0001t0012g0159 others(2): Show |
5 | HG01109.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-32691_29-32690i others(151): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368940 | ||||||
chr9:134368940 | G | GTGTGTGG others(141): Show |
4 | a0001c0001t0002g0001 a0001c0001t0009g0157 a0001c0001t0025g0158 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.29-32691_29-32690i others(150): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368940 | ||||||
chr9:134368940 | GTA | G | 4 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-32690_29-32689d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368940 | ||||||
chr9:134368942 | A | ATGTGTGT others(169): Show |
6 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
6 | HG01928.hp1 HG01978.hp2 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-32620_29-32619i others(178): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368942 | ||||||
chr9:134368942 | A | ATGTGTGT others(169): Show |
2 | a0001c0001t0001g0030 a0001c0001t0027g0086 |
2 | HG01346.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.29-32618_29-32617i others(178): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368942 | ||||||
chr9:134368942 | A | ATGTGTGT others(168): Show |
2 | a0001c0001t0004g0204 a0001c0001t0047g0116 |
2 | HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.29-32656_29-32655i others(177): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368942 | ||||||
chr9:134368942 | A | ATGTGTGT others(168): Show |
1 | a0001c0005t0001g0193 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.29-32656_29-32655i others(177): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368942 | ||||||
chr9:134368942 | A | ATGTGTGT others(167): Show |
19 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0004g0005 others(16): Show |
21 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.29-32656_29-32655i others(176): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368942 | ||||||
chr9:134368942 | A | ATGTGTGT others(166): Show |
2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.29-32656_29-32655i others(175): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368942 | ||||||
chr9:134368942 | A | ATGTGTGT others(167): Show |
37 | a0001c0001t0001g0046 a0001c0001t0001g0194 a0001c0001t0001g0218 others(34): Show |
37 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.29-32656_29-32655i others(176): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368942 | ||||||
chr9:134368942 | A | ATGTGTGT others(167): Show |
2 | a0001c0001t0001g0118 a0001c0001t0002g0212 |
2 | HG00621.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.29-32656_29-32655i others(176): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368942 | ||||||
chr9:134368942 | A | G | 10 | a0001c0001t0002g0001 a0001c0001t0004g0205 a0001c0001t0009g0157 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.29-32690A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368942 | |||||||
chr9:134368960 | G | C | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-32672G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134368960 | |||||||
chr9:134368970 | T | TGTGTGTG others(94): Show |
1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-32661_29-32660i others(103): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368970 | ||||||
chr9:134368975 | TTA | T | 8 | a0001c0001t0004g0160 a0001c0001t0005g0147 a0001c0001t0008g0141 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.29-32655_29-32654d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134368975 | ||||||
chr9:134369006 | G | GTGTGTGG others(186): Show |
1 | a0001c0004t0005g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.29-32620_29-32619i others(195): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369006 | ||||||
chr9:134369006 | G | GTGTGTGT others(11): Show |
1 | a0001c0001t0008g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.29-32618_29-32617i others(20): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369006 | ||||||
chr9:134369011 | TGTG | T | 10 | a0001c0001t0002g0001 a0001c0001t0004g0205 a0001c0001t0009g0157 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.29-32619_29-32617d others(5): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369011 | ||||||
chr9:134369012 | G | GGGGGGGG others(169): Show |
1 | a0001c0001t0004g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.29-32620_29-32619i others(178): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369012 | |||||||
chr9:134369012 | G | GGGGGGGG others(168): Show |
2 | a0001c0001t0008g0131 a0001c0001t0041g0139 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.29-32620_29-32619i others(177): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369012 | |||||||
chr9:134369013 | T | G | 6 | a0001c0001t0004g0202 a0001c0001t0008g0131 a0001c0001t0009g0130 others(3): Show |
6 | HG00735.hp2 HG02280.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-32619T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369013 | |||||||
chr9:134369013 | T | TG | 21 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0001t0001g0218 others(18): Show |
22 | HG00621.hp2 HG00738.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.29-32611dupG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369013 | ||||||
chr9:134369013 | T | TGTGGGGG others(167): Show |
3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.29-32618_29-32617i others(176): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369013 | ||||||
chr9:134369013 | T | TGTGGGGG others(169): Show |
1 | a0001c0001t0022g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.29-32618_29-32617i others(178): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369013 | ||||||
chr9:134369013 | T | TGTTGGGG others(157): Show |
1 | a0001c0001t0020g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-32618_29-32617i others(166): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369013 | ||||||
chr9:134369014 | G | GT | 45 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0123 others(42): Show |
46 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.29-32618_29-32617i others(3): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369014 | |||||||
chr9:134369015 | G | GGGGGGGT others(188): Show |
1 | a0001c0001t0004g0160 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.29-32600_29-32599i others(197): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369015 | ||||||
chr9:134369015 | G | GGGGGGGT others(187): Show |
1 | a0001c0001t0005g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.29-32600_29-32599i others(196): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369015 | ||||||
chr9:134369015 | G | GGGGGGTT others(186): Show |
1 | a0001c0001t0026g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.29-32612_29-32611i others(195): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369015 | ||||||
chr9:134369015 | G | T | 2 | a0001c0001t0008g0087 a0001c0004t0005g0126 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.29-32617G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369015 | |||||||
chr9:134369024 | A | G | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.29-32608A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369024 | |||||||
chr9:134369033 | T | G | 21 | a0001c0001t0001g0030 a0001c0001t0001g0092 a0001c0001t0001g0093 others(18): Show |
21 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.29-32599T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369033 | |||||||
chr9:134369033 | T | TGGGGGGT others(170): Show |
2 | a0001c0001t0001g0135 a0001c0001t0004g0129 |
2 | HG02055.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.29-32585_29-32584i others(179): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(169): Show |
8 | a0001c0001t0003g0166 a0001c0001t0004g0128 a0001c0001t0008g0037 others(5): Show |
8 | HG01243.hp1 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-32585_29-32584i others(178): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(169): Show |
1 | a0001c0001t0009g0138 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.29-32585_29-32584i others(178): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(171): Show |
1 | a0001c0001t0059g0210 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.29-32545_29-32544i others(180): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(170): Show |
10 | a0001c0001t0001g0164 a0001c0001t0004g0148 a0001c0001t0009g0098 others(7): Show |
10 | HG01943.hp2 HG02109.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.29-32545_29-32544i others(179): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(170): Show |
1 | a0001c0001t0001g0089 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.29-32545_29-32544i others(179): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(169): Show |
1 | a0001c0001t0002g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.29-32545_29-32544i others(178): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(169): Show |
3 | a0001c0001t0001g0049 a0001c0001t0006g0021 a0001c0001t0038g0074 |
3 | HG00099.hp1 HG00140.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.29-32545_29-32544i others(178): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(170): Show |
2 | a0001c0001t0005g0165 a0001c0001t0050g0042 |
2 | HG03540.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.29-32545_29-32544i others(179): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(169): Show |
87 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(84): Show |
88 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.29-32545_29-32544i others(178): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(170): Show |
1 | a0001c0001t0001g0050 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.29-32545_29-32544i others(179): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(169): Show |
1 | a0001c0001t0004g0209 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.29-32545_29-32544i others(178): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(169): Show |
5 | a0001c0001t0003g0080 a0001c0001t0003g0142 a0001c0001t0004g0133 others(2): Show |
5 | HG00735.hp1 HG02145.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-32545_29-32544i others(178): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369033 | T | TGGGGGGT others(169): Show |
1 | a0001c0001t0007g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.29-32545_29-32544i others(178): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369033 | ||||||
chr9:134369078 | G | C | 9 | a0001c0001t0002g0001 a0001c0001t0004g0205 a0001c0001t0009g0157 others(6): Show |
11 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.29-32554G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369078 | |||||||
chr9:134369105 | G | GAGTGC | 2 | a0001c0001t0010g0101 a0001c0001t0024g0172 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.29-32527_29-32526i others(7): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369105 | |||||||
chr9:134369106 | T | C | 2 | a0001c0001t0010g0101 a0001c0001t0024g0172 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.29-32526T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369106 | |||||||
chr9:134369111 | T | TTATG | 2 | a0001c0001t0010g0101 a0001c0001t0024g0172 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.29-32520_29-32519i others(6): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369111 | ||||||
chr9:134369125 | A | G | 2 | a0001c0001t0010g0101 a0001c0001t0024g0172 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.29-32507A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369125 | |||||||
chr9:134369130 | T | TTG | 79 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(76): Show |
83 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.29-32495_29-32494d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369130 | ||||||
chr9:134369131 | TG | T | 5 | a0001c0001t0004g0160 a0001c0001t0005g0147 a0001c0001t0008g0087 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-32500delG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369131 | |||||||
chr9:134369153 | T | A | 1 | a0001c0001t0004g0160 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.29-32479T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369153 | |||||||
chr9:134369284 | GT | G | 3 | a0001c0001t0004g0133 a0001c0001t0007g0119 a0001c0001t0007g0203 |
3 | HG02258.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.29-32347delT | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369284 | |||||||
chr9:134369287 | T | G | 3 | a0001c0001t0004g0133 a0001c0001t0007g0119 a0001c0001t0007g0203 |
3 | HG02258.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.29-32345T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369287 | |||||||
chr9:134369287 | TG | T | 36 | a0001c0001t0001g0046 a0001c0001t0001g0194 a0001c0001t0001g0218 others(33): Show |
36 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.29-32340delG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369287 | ||||||
chr9:134369295 | A | ATGTGTGT others(458): Show |
2 | a0001c0001t0008g0141 a0001c0001t0056g0143 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.29-32306_29-32305i others(467): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369295 | ||||||
chr9:134369316 | TTG | T | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.29-32307_29-32306d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369316 | ||||||
chr9:134369325 | T | G | 1 | a0001c0001t0006g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.29-32307T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369325 | |||||||
chr9:134369325 | TG | T | 24 | a0001c0001t0001g0135 a0001c0001t0001g0164 a0001c0001t0003g0166 others(21): Show |
24 | HG01243.hp1 HG01943.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.29-32299delG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134369325 | ||||||
chr9:134369327 | G | T | 18 | a0001c0001t0002g0001 a0001c0001t0004g0160 a0001c0001t0004g0205 others(15): Show |
20 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.29-32305G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369327 | |||||||
chr9:134369392 | A | G | 85 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(82): Show |
89 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.29-32240A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369392 | |||||||
chr9:134369416 | A | T | 17 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0118 others(14): Show |
18 | HG00621.hp2 HG00733.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.29-32216A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369416 | |||||||
chr9:134369524 | G | T | 1 | a0001c0001t0007g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.29-32108G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369524 | |||||||
chr9:134369564 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.29-32068C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369564 | |||||||
chr9:134369597 | G | A | 1 | a0001c0001t0020g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-32035G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369597 | |||||||
chr9:134369640 | C | T | 32 | a0001c0001t0001g0135 a0001c0001t0001g0164 a0001c0001t0003g0166 others(29): Show |
32 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.29-31992C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369640 | |||||||
chr9:134369648 | C | T | 9 | a0001c0001t0002g0001 a0001c0001t0004g0205 a0001c0001t0009g0157 others(6): Show |
11 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.29-31984C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369648 | |||||||
chr9:134369664 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.29-31968T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369664 | |||||||
chr9:134369757 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.29-31875G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369757 | |||||||
chr9:134369786 | C | T | 75 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(72): Show |
79 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.29-31846C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369786 | |||||||
chr9:134369911 | G | A | 2 | a0001c0001t0008g0141 a0001c0001t0056g0143 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.29-31721G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369911 | |||||||
chr9:134369930 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.29-31702G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369930 | |||||||
chr9:134369945 | G | A | 4 | a0001c0001t0004g0133 a0001c0001t0007g0119 a0001c0001t0007g0203 others(1): Show |
4 | HG01255.hp1 HG02258.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-31687G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369945 | |||||||
chr9:134369993 | C | T | 3 | a0001c0001t0005g0165 a0001c0001t0008g0131 a0001c0001t0041g0139 |
3 | HG02723.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.29-31639C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369993 | |||||||
chr9:134369994 | G | A | 69 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(66): Show |
73 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.29-31638G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134369994 | |||||||
chr9:134370148 | C | T | 1 | a0001c0001t0060g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.29-31484C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370148 | |||||||
chr9:134370169 | C | A | 1 | a0001c0001t0008g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.29-31463C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370169 | |||||||
chr9:134370261 | T | C | 78 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(75): Show |
82 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.29-31371T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370261 | |||||||
chr9:134370266 | C | T | 5 | a0001c0001t0004g0160 a0001c0001t0005g0147 a0001c0001t0008g0087 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-31366C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370266 | |||||||
chr9:134370270 | C | T | 75 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(72): Show |
79 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.29-31362C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370270 | |||||||
chr9:134370273 | T | C | 78 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(75): Show |
82 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.29-31359T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370273 | |||||||
chr9:134370292 | G | A | 5 | a0001c0001t0004g0160 a0001c0001t0005g0147 a0001c0001t0008g0087 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-31340G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370292 | |||||||
chr9:134370519 | G | T | 2 | a0001c0001t0002g0001 a0001c0001t0020g0154 |
4 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-31113G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370519 | |||||||
chr9:134370633 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.29-30999C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370633 | |||||||
chr9:134370743 | C | T | 2 | a0001c0001t0008g0141 a0001c0001t0056g0143 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.29-30889C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370743 | |||||||
chr9:134370754 | G | T | 2 | a0001c0001t0008g0141 a0001c0001t0056g0143 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.29-30878G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370754 | |||||||
chr9:134370817 | T | C | 78 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(75): Show |
82 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.29-30815T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370817 | |||||||
chr9:134370818 | G | A | 5 | a0001c0001t0004g0160 a0001c0001t0005g0147 a0001c0001t0008g0087 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-30814G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370818 | |||||||
chr9:134370854 | G | A | 1 | a0001c0001t0008g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.29-30778G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370854 | |||||||
chr9:134370927 | A | C | 2 | a0001c0001t0008g0141 a0001c0001t0056g0143 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.29-30705A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134370927 | |||||||
chr9:134371023 | T | C | 1 | a0001c0001t0031g0065 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.29-30609T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134371023 | |||||||
chr9:134371181 | C | T | 2 | a0001c0001t0005g0004 a0001c0001t0043g0004 |
2 | NA18955.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.29-30451C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134371181 | |||||||
chr9:134371304 | C | G | 5 | a0001c0001t0004g0160 a0001c0001t0005g0147 a0001c0001t0008g0087 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-30328C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134371304 | |||||||
chr9:134371347 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.29-30285C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134371347 | |||||||
chr9:134371394 | T | C | 8 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(5): Show |
8 | HG00642.hp1 HG01109.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-30238T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134371394 | |||||||
chr9:134371535 | C | G | 3 | a0001c0001t0005g0165 a0001c0001t0008g0131 a0001c0001t0041g0139 |
3 | HG02723.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.29-30097C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134371535 | |||||||
chr9:134371712 | C | T | 1 | a0001c0001t0022g0134 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.29-29920C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134371712 | |||||||
chr9:134371811 | C | T | 5 | a0001c0001t0004g0160 a0001c0001t0005g0147 a0001c0001t0008g0087 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-29821C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134371811 | |||||||
chr9:134371821 | C | T | 1 | a0001c0001t0008g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.29-29811C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134371821 | |||||||
chr9:134372088 | T | C | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.29-29544T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134372088 | |||||||
chr9:134372172 | C | A | 79 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(76): Show |
83 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.29-29460C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134372172 | |||||||
chr9:134372196 | T | C | 79 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(76): Show |
83 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.29-29436T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134372196 | |||||||
chr9:134372243 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-29389C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134372243 | |||||||
chr9:134372364 | G | A | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.29-29268G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134372364 | |||||||
chr9:134372500 | T | C | 92 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(89): Show |
96 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.29-29132T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134372500 | |||||||
chr9:134372529 | TAGAGGGC others(25): Show |
T | 1 | a0001c0001t0001g0088 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.29-29078_29-29047d others(34): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134372529 | ||||||
chr9:134372657 | G | A | 5 | a0001c0001t0004g0160 a0001c0001t0005g0147 a0001c0001t0008g0087 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-28975G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134372657 | |||||||
chr9:134372688 | T | C | 23 | a0001c0001t0001g0135 a0001c0001t0001g0164 a0001c0001t0003g0166 others(20): Show |
23 | HG01243.hp1 HG01943.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.29-28944T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134372688 | |||||||
chr9:134372789 | G | A | 1 | a0001c0001t0002g0110 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.29-28843G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134372789 | |||||||
chr9:134372843 | T | G | 2 | a0001c0001t0004g0195 a0001c0001t0062g0120 |
2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.29-28789T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134372843 | |||||||
chr9:134372866 | A | G | 63 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(60): Show |
65 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.29-28766A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134372866 | |||||||
chr9:134372868 | C | G | 1 | a0001c0001t0003g0224 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.29-28764C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134372868 | |||||||
chr9:134373039 | C | T | 1 | a0001c0001t0020g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-28593C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373039 | |||||||
chr9:134373046 | G | A | 5 | a0001c0001t0004g0160 a0001c0001t0005g0147 a0001c0001t0008g0087 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-28586G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373046 | |||||||
chr9:134373159 | T | C | 10 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 others(7): Show |
10 | HG00642.hp1 HG01109.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.29-28473T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373159 | |||||||
chr9:134373204 | C | T | 2 | a0001c0001t0002g0001 a0001c0001t0020g0154 |
4 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-28428C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373204 | |||||||
chr9:134373223 | G | A | 1 | a0001c0001t0020g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-28409G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373223 | |||||||
chr9:134373250 | G | T | 2 | a0001c0001t0011g0132 a0001c0001t0014g0173 |
2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.29-28382G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373250 | |||||||
chr9:134373321 | C | T | 5 | a0001c0001t0002g0001 a0001c0001t0010g0101 a0001c0001t0020g0154 others(2): Show |
7 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-28311C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373321 | |||||||
chr9:134373378 | C | G | 1 | a0001c0001t0007g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.29-28254C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373378 | |||||||
chr9:134373386 | C | T | 2 | a0001c0001t0011g0132 a0001c0001t0014g0173 |
2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.29-28246C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373386 | |||||||
chr9:134373412 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.29-28220G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373412 | |||||||
chr9:134373430 | T | C | 79 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(76): Show |
83 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.29-28202T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373430 | |||||||
chr9:134373433 | T | G | 217 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(214): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.29-28199T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373433 | |||||||
chr9:134373448 | G | GC | 5 | a0001c0001t0004g0160 a0001c0001t0005g0147 a0001c0001t0008g0087 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-28181dupC | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134373448 | ||||||
chr9:134373497 | G | A | 1 | a0001c0001t0046g0152 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.29-28135G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373497 | |||||||
chr9:134373515 | G | A | 36 | a0001c0001t0001g0046 a0001c0001t0001g0194 a0001c0001t0001g0218 others(33): Show |
36 | HG00597.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.29-28117G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373515 | |||||||
chr9:134373515 | G | C | 1 | a0001c0001t0002g0052 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.29-28117G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373515 | |||||||
chr9:134373518 | G | A | 2 | a0001c0001t0006g0181 a0001c0001t0014g0180 |
2 | HG01256.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.29-28114G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373518 | |||||||
chr9:134373698 | C | T | 1 | a0001c0001t0005g0144 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.29-27934C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373698 | |||||||
chr9:134373863 | C | T | 5 | a0001c0001t0004g0160 a0001c0001t0005g0147 a0001c0001t0008g0087 others(2): Show |
5 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-27769C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373863 | |||||||
chr9:134373914 | A | T | 1 | a0001c0001t0016g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.29-27718A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373914 | |||||||
chr9:134373959 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.29-27673G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373959 | |||||||
chr9:134373995 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.29-27637G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134373995 | |||||||
chr9:134374019 | C | T | 5 | a0001c0001t0002g0097 a0001c0001t0003g0043 a0001c0001t0003g0044 others(2): Show |
5 | NA18939.hp1 NA18954.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-27613C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374019 | |||||||
chr9:134374035 | C | T | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.29-27597C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374035 | |||||||
chr9:134374043 | C | T | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.29-27589C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374043 | |||||||
chr9:134374073 | G | A | 1 | a0001c0001t0004g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.29-27559G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374073 | |||||||
chr9:134374242 | G | T | 1 | a0001c0001t0003g0025 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.29-27390G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374242 | |||||||
chr9:134374298 | G | A | 1 | a0001c0001t0004g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.29-27334G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374298 | |||||||
chr9:134374373 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.29-27259C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374373 | |||||||
chr9:134374403 | G | C | 1 | a0001c0001t0008g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.29-27229G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374403 | |||||||
chr9:134374537 | C | G | 4 | a0001c0001t0005g0147 a0001c0001t0008g0087 a0001c0001t0026g0127 others(1): Show |
4 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-27095C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374537 | |||||||
chr9:134374593 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.29-27039A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374593 | |||||||
chr9:134374606 | C | T | 1 | a0001c0001t0002g0082 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.29-27026C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374606 | |||||||
chr9:134374617 | C | T | 1 | a0001c0001t0007g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.29-27015C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374617 | |||||||
chr9:134374631 | A | G | 18 | a0001c0001t0001g0135 a0001c0001t0001g0164 a0001c0001t0003g0166 others(15): Show |
18 | HG01243.hp1 HG01943.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.29-27001A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374631 | |||||||
chr9:134374705 | T | A | 2 | a0001c0001t0002g0001 a0001c0001t0020g0154 |
4 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-26927T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374705 | |||||||
chr9:134374858 | A | C | 26 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0118 others(23): Show |
28 | HG00621.hp2 HG00733.hp2 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.29-26774A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374858 | |||||||
chr9:134374947 | C | G | 4 | a0001c0001t0005g0147 a0001c0001t0008g0087 a0001c0001t0026g0127 others(1): Show |
4 | HG01891.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-26685C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134374947 | |||||||
chr9:134375250 | G | A | 1 | a0001c0001t0020g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-26382G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375250 | |||||||
chr9:134375280 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0003g0009 a0001c0001t0003g0010 |
3 | HG00642.hp1 HG01109.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.29-26352C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375280 | |||||||
chr9:134375326 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.29-26306C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375326 | |||||||
chr9:134375593 | T | C | 119 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(116): Show |
123 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.29-26039T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375593 | |||||||
chr9:134375618 | A | C | 1 | a0001c0001t0006g0181 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.29-26014A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375618 | |||||||
chr9:134375722 | G | A | 1 | a0001c0001t0006g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.29-25910G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375722 | |||||||
chr9:134375758 | C | T | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.29-25874C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375758 | |||||||
chr9:134375830 | G | T | 1 | a0001c0001t0020g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-25802G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375830 | |||||||
chr9:134375833 | A | G | 118 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(115): Show |
122 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(119): Show |
intron_variant | MODIFIER | c.29-25799A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375833 | |||||||
chr9:134375880 | C | T | 3 | a0001c0001t0005g0165 a0001c0001t0008g0131 a0001c0001t0041g0139 |
3 | HG02723.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.29-25752C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375880 | |||||||
chr9:134375894 | C | T | 2 | a0001c0001t0008g0131 a0001c0001t0041g0139 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.29-25738C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375894 | |||||||
chr9:134375933 | GCCCT | G | 2 | a0001c0001t0004g0005 a0001c0001t0006g0021 |
3 | HG01099.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.29-25681_29-25678d others(6): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134375933 | ||||||
chr9:134375937 | T | G | 117 | a0001c0001t0001g0046 a0001c0001t0001g0112 a0001c0001t0001g0113 others(114): Show |
120 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(117): Show |
intron_variant | MODIFIER | c.29-25695T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375937 | |||||||
chr9:134375941 | T | G | 2 | a0001c0001t0004g0005 a0001c0001t0006g0021 |
3 | HG01099.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.29-25691T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134375941 | |||||||
chr9:134375951 | CCTCT | C | 12 | a0001c0001t0002g0001 a0001c0001t0004g0148 a0001c0001t0010g0101 others(9): Show |
14 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-25672_29-25669d others(6): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134375951 | ||||||
chr9:134376145 | C | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.29-25487C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376145 | |||||||
chr9:134376167 | C | T | 1 | a0001c0001t0020g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-25465C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376167 | |||||||
chr9:134376198 | T | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.29-25434T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376198 | |||||||
chr9:134376217 | A | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.29-25415A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376217 | |||||||
chr9:134376261 | A | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.29-25371A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376261 | |||||||
chr9:134376331 | C | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.29-25301C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376331 | |||||||
chr9:134376385 | C | T | 1 | a0001c0001t0006g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.29-25247C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376385 | |||||||
chr9:134376399 | T | G | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.29-25233T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376399 | |||||||
chr9:134376405 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.29-25227C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376405 | |||||||
chr9:134376473 | C | T | 1 | a0001c0001t0024g0172 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.29-25159C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376473 | |||||||
chr9:134376493 | C | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.29-25139C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376493 | |||||||
chr9:134376586 | T | TTGCCGCG others(56): Show |
2 | a0001c0001t0005g0165 a0001c0001t0008g0131 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.29-25038_29-25037i others(65): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134376586 | ||||||
chr9:134376595 | T | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.29-25037T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376595 | |||||||
chr9:134376620 | A | C | 1 | a0001c0001t0041g0139 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.29-25012A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376620 | |||||||
chr9:134376627 | T | A | 2 | a0001c0001t0005g0165 a0001c0001t0008g0131 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.29-25005T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376627 | |||||||
chr9:134376627 | T | TCTCAGAG others(56): Show |
147 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(144): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.29-24980_29-24979i others(65): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134376627 | ||||||
chr9:134376680 | C | G | 5 | a0001c0001t0003g0142 a0001c0001t0008g0125 a0001c0001t0010g0122 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-24952C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376680 | |||||||
chr9:134376836 | C | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.29-24796C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376836 | |||||||
chr9:134376862 | G | A | 13 | a0001c0001t0001g0175 a0001c0001t0001g0211 a0001c0001t0002g0052 others(10): Show |
13 | HG00408.hp1 HG02083.hp1 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.29-24770G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376862 | |||||||
chr9:134376931 | C | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.29-24701C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134376931 | |||||||
chr9:134377069 | T | C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.29-24563T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377069 | |||||||
chr9:134377289 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.29-24343C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377289 | |||||||
chr9:134377316 | G | A | 2 | a0001c0001t0008g0131 a0001c0001t0041g0139 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.29-24316G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377316 | |||||||
chr9:134377329 | T | A | 12 | a0001c0001t0003g0142 a0001c0001t0004g0205 a0001c0001t0008g0125 others(9): Show |
12 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.29-24303T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377329 | |||||||
chr9:134377423 | G | A | 1 | a0001c0001t0005g0183 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.29-24209G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377423 | |||||||
chr9:134377480 | C | T | 1 | a0001c0001t0004g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.29-24152C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377480 | |||||||
chr9:134377494 | T | C | 222 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(219): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.29-24138T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377494 | |||||||
chr9:134377496 | C | T | 1 | a0001c0001t0061g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.29-24136C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377496 | |||||||
chr9:134377536 | T | C | 1 | a0001c0001t0020g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.29-24096T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377536 | |||||||
chr9:134377557 | C | A | 8 | a0001c0001t0002g0185 a0001c0001t0002g0187 a0001c0001t0002g0226 others(5): Show |
8 | HG00597.hp2 HG02027.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.29-24075C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377557 | |||||||
chr9:134377610 | T | C | 85 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0028 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.29-24022T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377610 | |||||||
chr9:134377621 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.29-24011A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377621 | |||||||
chr9:134377711 | A | C | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-23921A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377711 | |||||||
chr9:134377724 | C | A | 15 | a0001c0001t0001g0118 a0001c0001t0001g0164 a0001c0001t0002g0179 others(12): Show |
16 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.29-23908C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377724 | |||||||
chr9:134377761 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(139): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.29-23871C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377761 | |||||||
chr9:134377836 | A | C | 24 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0001t0001g0123 others(21): Show |
26 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.29-23796A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377836 | |||||||
chr9:134377916 | C | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.29-23716C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377916 | |||||||
chr9:134377950 | C | T | 1 | a0001c0001t0053g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.29-23682C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377950 | |||||||
chr9:134377951 | G | A | 2 | a0001c0001t0003g0009 a0001c0001t0003g0010 |
2 | HG00642.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.29-23681G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377951 | |||||||
chr9:134377974 | T | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.29-23658T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377974 | |||||||
chr9:134377989 | G | A | 138 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.29-23643G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377989 | |||||||
chr9:134377991 | C | T | 4 | a0001c0001t0008g0125 a0001c0001t0010g0122 a0001c0001t0011g0121 others(1): Show |
4 | HG01891.hp2 HG02559.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-23641C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134377991 | |||||||
chr9:134378113 | G | A | 1 | a0001c0001t0020g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-23519G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378113 | |||||||
chr9:134378143 | G | A | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.29-23489G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378143 | |||||||
chr9:134378163 | G | A | 13 | a0001c0001t0002g0001 a0001c0001t0004g0005 a0001c0001t0004g0153 others(10): Show |
16 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.29-23469G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378163 | |||||||
chr9:134378285 | C | T | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.29-23347C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378285 | |||||||
chr9:134378342 | T | C | 3 | a0001c0001t0020g0154 a0001c0001t0020g0182 a0001c0001t0022g0208 |
3 | HG02976.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.29-23290T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378342 | |||||||
chr9:134378350 | G | GGCCAGCG others(7): Show |
117 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.29-23279_29-23266d others(16): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134378350 | ||||||
chr9:134378370 | G | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(81): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.29-23262G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378370 | |||||||
chr9:134378393 | C | G | 2 | a0001c0001t0026g0127 a0001c0004t0005g0126 |
2 | HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.29-23239C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378393 | |||||||
chr9:134378527 | G | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.29-23105G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378527 | |||||||
chr9:134378530 | C | G | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.29-23102C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378530 | |||||||
chr9:134378715 | C | A | 1 | a0001c0001t0017g0057 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.29-22917C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378715 | |||||||
chr9:134378721 | G | C | 7 | a0001c0001t0004g0148 a0001c0001t0005g0165 a0001c0001t0015g0102 others(4): Show |
7 | HG01255.hp2 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-22911G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378721 | |||||||
chr9:134378769 | C | T | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-22863C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378769 | |||||||
chr9:134378796 | C | A | 6 | a0001c0001t0001g0050 a0001c0001t0001g0217 a0001c0001t0002g0048 others(3): Show |
6 | HG00738.hp1 HG01074.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-22836C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378796 | |||||||
chr9:134378798 | C | T | 3 | a0001c0001t0020g0154 a0001c0001t0020g0182 a0001c0001t0022g0208 |
3 | HG02976.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.29-22834C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378798 | |||||||
chr9:134378843 | C | T | 1 | a0001c0001t0032g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.29-22789C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378843 | |||||||
chr9:134378866 | G | C | 7 | a0001c0001t0004g0148 a0001c0001t0005g0165 a0001c0001t0015g0102 others(4): Show |
7 | HG01255.hp2 HG02109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-22766G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378866 | |||||||
chr9:134378935 | G | C | 4 | a0001c0001t0005g0147 a0001c0001t0008g0131 a0001c0001t0009g0130 others(1): Show |
4 | HG01891.hp1 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-22697G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378935 | |||||||
chr9:134378936 | C | T | 4 | a0001c0001t0005g0147 a0001c0001t0008g0131 a0001c0001t0009g0130 others(1): Show |
4 | HG01891.hp1 HG02723.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-22696C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134378936 | |||||||
chr9:134379022 | G | A | 1 | a0001c0001t0031g0065 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.29-22610G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379022 | |||||||
chr9:134379096 | C | A | 1 | a0001c0001t0007g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.29-22536C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379096 | |||||||
chr9:134379171 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29-22461C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379171 | |||||||
chr9:134379227 | TGATCCCT others(4): Show |
T | 14 | a0001c0001t0004g0148 a0001c0001t0005g0165 a0001c0001t0009g0157 others(11): Show |
14 | HG01109.hp1 HG01255.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.29-22403_29-22393d others(13): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134379227 | ||||||
chr9:134379288 | C | T | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.29-22344C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379288 | |||||||
chr9:134379411 | G | A | 1 | a0001c0001t0061g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.29-22221G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379411 | |||||||
chr9:134379455 | C | G | 3 | a0001c0001t0008g0087 a0001c0001t0026g0127 a0001c0004t0005g0126 |
3 | HG02717.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.29-22177C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379455 | |||||||
chr9:134379455 | C | T | 1 | a0001c0001t0027g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.29-22177C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379455 | |||||||
chr9:134379472 | C | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(96): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.29-22160C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379472 | |||||||
chr9:134379505 | G | A | 3 | a0001c0001t0002g0001 a0001c0001t0004g0204 a0001c0001t0061g0156 |
5 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-22127G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379505 | |||||||
chr9:134379531 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.29-22101G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379531 | |||||||
chr9:134379538 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.29-22094A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379538 | |||||||
chr9:134379562 | G | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(107): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.29-22070G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379562 | |||||||
chr9:134379608 | A | G | 172 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(169): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.29-22024A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379608 | |||||||
chr9:134379627 | C | T | 16 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0128 others(13): Show |
16 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.29-22005C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379627 | |||||||
chr9:134379768 | G | A | 1 | a0001c0001t0057g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.29-21864G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379768 | |||||||
chr9:134379781 | G | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(107): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.29-21851G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379781 | |||||||
chr9:134379870 | C | T | 2 | a0001c0001t0008g0131 a0001c0001t0041g0139 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.29-21762C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379870 | |||||||
chr9:134379871 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(78): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.29-21761G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379871 | |||||||
chr9:134379910 | C | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(107): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.29-21722C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379910 | |||||||
chr9:134379975 | C | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.29-21657C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134379975 | |||||||
chr9:134380148 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.29-21484C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380148 | |||||||
chr9:134380232 | C | T | 4 | a0001c0001t0005g0020 a0001c0001t0008g0087 a0001c0001t0026g0127 others(1): Show |
4 | HG02717.hp2 HG02976.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-21400C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380232 | |||||||
chr9:134380375 | C | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.29-21257C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380375 | |||||||
chr9:134380382 | A | C | 1 | a0001c0001t0002g0031 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.29-21250A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380382 | |||||||
chr9:134380399 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(103): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.29-21233C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380399 | |||||||
chr9:134380434 | G | A | 5 | a0001c0001t0003g0142 a0001c0001t0008g0125 a0001c0001t0010g0122 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-21198G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380434 | |||||||
chr9:134380494 | GC | G | 121 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(118): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.29-21131delC | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134380494 | ||||||
chr9:134380648 | G | A | 6 | a0001c0001t0001g0050 a0001c0001t0001g0217 a0001c0001t0002g0048 others(3): Show |
6 | HG00738.hp1 HG01074.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-20984G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380648 | |||||||
chr9:134380656 | A | G | 105 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(102): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.29-20976A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380656 | |||||||
chr9:134380748 | C | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(166): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.29-20884C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380748 | |||||||
chr9:134380786 | C | G | 23 | a0001c0001t0001g0135 a0001c0001t0001g0175 a0001c0001t0002g0052 others(20): Show |
23 | HG00408.hp1 HG01192.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.29-20846C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380786 | |||||||
chr9:134380797 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(104): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.29-20835G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380797 | |||||||
chr9:134380822 | C | T | 2 | a0001c0001t0016g0207 a0001c0001t0039g0206 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.29-20810C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380822 | |||||||
chr9:134380872 | A | G | 6 | a0001c0001t0001g0050 a0001c0001t0001g0217 a0001c0001t0002g0048 others(3): Show |
6 | HG00738.hp1 HG01074.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-20760A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380872 | |||||||
chr9:134380877 | C | T | 3 | a0001c0001t0008g0087 a0001c0001t0026g0127 a0001c0004t0005g0126 |
3 | HG02717.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.29-20755C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380877 | |||||||
chr9:134380994 | A | T | 118 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(115): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.29-20638A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134380994 | |||||||
chr9:134381087 | C | T | 6 | a0001c0001t0001g0050 a0001c0001t0001g0217 a0001c0001t0002g0048 others(3): Show |
6 | HG00738.hp1 HG01074.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-20545C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134381087 | |||||||
chr9:134381113 | G | A | 7 | a0001c0001t0002g0001 a0001c0001t0004g0204 a0001c0001t0008g0125 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.29-20519G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134381113 | |||||||
chr9:134381241 | G | A | 1 | a0001c0001t0036g0201 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.29-20391G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134381241 | |||||||
chr9:134381256 | G | A | 1 | a0001c0001t0005g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.29-20376G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134381256 | |||||||
chr9:134381287 | A | G | 215 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(212): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.29-20345A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134381287 | |||||||
chr9:134381328 | GAGCTC | G | 47 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0001t0001g0123 others(44): Show |
48 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.29-20301_29-20297d others(7): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134381328 | ||||||
chr9:134381344 | T | G | 6 | a0001c0001t0001g0050 a0001c0001t0001g0217 a0001c0001t0002g0048 others(3): Show |
6 | HG00738.hp1 HG01074.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-20288T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134381344 | |||||||
chr9:134381704 | C | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(175): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.29-19928C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134381704 | |||||||
chr9:134381847 | T | G | 7 | a0001c0001t0009g0157 a0001c0001t0012g0038 a0001c0001t0012g0151 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-19785T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134381847 | |||||||
chr9:134381942 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.29-19690G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134381942 | |||||||
chr9:134381961 | G | A | 2 | a0001c0001t0002g0082 a0001c0001t0002g0226 |
2 | NA19010.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.29-19671G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134381961 | |||||||
chr9:134382012 | T | G | 4 | a0001c0001t0003g0142 a0001c0001t0008g0125 a0001c0001t0010g0122 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-19620T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382012 | |||||||
chr9:134382025 | C | T | 3 | a0001c0001t0008g0087 a0001c0001t0026g0127 a0001c0004t0005g0126 |
3 | HG02717.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.29-19607C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382025 | |||||||
chr9:134382125 | T | TG | 142 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(139): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.29-19500dupG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134382125 | ||||||
chr9:134382128 | G | C | 23 | a0001c0001t0001g0135 a0001c0001t0004g0128 a0001c0001t0004g0129 others(20): Show |
23 | HG01109.hp1 HG01255.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.29-19504G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382128 | |||||||
chr9:134382133 | C | G | 68 | a0001c0001t0001g0135 a0001c0001t0002g0001 a0001c0001t0002g0052 others(65): Show |
71 | HG00408.hp1 HG00597.hp2 HG01069.hp1 others(68): Show |
intron_variant | MODIFIER | c.29-19499C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382133 | |||||||
chr9:134382199 | C | T | 4 | a0001c0001t0007g0090 a0001c0001t0008g0141 a0001c0001t0027g0086 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-19433C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382199 | |||||||
chr9:134382233 | C | T | 1 | a0001c0001t0061g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.29-19399C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382233 | |||||||
chr9:134382268 | GGT | G | 13 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0001t0001g0123 others(10): Show |
13 | HG00621.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.29-19340_29-19339d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134382268 | ||||||
chr9:134382268 | GGTGT | G | 13 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0081 others(10): Show |
13 | HG00735.hp1 HG01099.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-19342_29-19339d others(6): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134382268 | ||||||
chr9:134382292 | T | C | 1 | a0001c0001t0004g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.29-19340T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382292 | |||||||
chr9:134382292 | T | TGC | 3 | a0001c0001t0004g0195 a0001c0001t0060g0100 a0001c0001t0062g0120 |
3 | HG02717.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.29-19337_29-19336d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134382292 | ||||||
chr9:134382376 | G | C | 12 | a0001c0001t0003g0166 a0001c0001t0008g0037 a0001c0001t0009g0157 others(9): Show |
12 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.29-19256G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382376 | |||||||
chr9:134382432 | C | T | 1 | a0001c0001t0004g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.29-19200C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382432 | |||||||
chr9:134382473 | G | A | 1 | a0001c0002t0040g0040 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.29-19159G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382473 | |||||||
chr9:134382542 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.29-19090G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382542 | |||||||
chr9:134382578 | A | G | 2 | a0001c0001t0018g0104 a0001c0001t0018g0105 |
2 | NA18944.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.29-19054A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382578 | |||||||
chr9:134382724 | A | G | 1 | a0001c0001t0060g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.29-18908A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382724 | |||||||
chr9:134382785 | G | A | 2 | a0001c0001t0003g0166 a0001c0001t0008g0037 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.29-18847G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382785 | |||||||
chr9:134382880 | C | G | 4 | a0001c0001t0007g0090 a0001c0001t0008g0141 a0001c0001t0027g0086 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-18752C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382880 | |||||||
chr9:134382960 | C | T | 3 | a0001c0001t0008g0087 a0001c0001t0026g0127 a0001c0004t0005g0126 |
3 | HG02717.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.29-18672C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382960 | |||||||
chr9:134382967 | C | T | 10 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0001t0001g0123 others(7): Show |
11 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.29-18665C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134382967 | |||||||
chr9:134383181 | A | G | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0015g0168 others(1): Show |
4 | HG02451.hp2 HG03471.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-18451A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134383181 | |||||||
chr9:134383612 | G | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(77): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.29-18020G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134383612 | |||||||
chr9:134383617 | A | C | 14 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0081 others(11): Show |
14 | HG00735.hp1 HG01099.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-18015A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134383617 | |||||||
chr9:134383957 | C | T | 10 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0001t0001g0123 others(7): Show |
11 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.29-17675C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134383957 | |||||||
chr9:134383995 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.29-17637G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134383995 | |||||||
chr9:134384082 | TGGGGAGT others(29): Show |
T | 3 | a0001c0001t0001g0175 a0001c0001t0003g0174 a0001c0001t0055g0167 |
3 | HG01257.hp1 NA18969.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.29-17540_29-17505d others(38): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134384082 | ||||||
chr9:134384152 | G | A | 1 | a0001c0001t0007g0203 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.29-17480G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134384152 | |||||||
chr9:134384191 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(79): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.29-17441G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134384191 | |||||||
chr9:134384225 | G | C | 2 | a0001c0001t0008g0131 a0001c0001t0041g0139 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.29-17407G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134384225 | |||||||
chr9:134384285 | G | A | 41 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0005 others(38): Show |
42 | HG00735.hp2 HG01109.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.29-17347G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134384285 | |||||||
chr9:134384370 | G | A | 36 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0005 others(33): Show |
37 | HG00735.hp2 HG01109.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.29-17262G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134384370 | |||||||
chr9:134384602 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.29-17030C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134384602 | |||||||
chr9:134384621 | C | T | 5 | a0001c0001t0004g0225 a0001c0001t0016g0115 a0001c0001t0016g0155 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-17011C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134384621 | |||||||
chr9:134384626 | T | TG | 10 | a0001c0001t0008g0131 a0001c0001t0009g0157 a0001c0001t0012g0038 others(7): Show |
10 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.29-17000dupG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134384626 | ||||||
chr9:134384712 | C | T | 1 | a0001c0001t0004g0209 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.29-16920C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134384712 | |||||||
chr9:134384830 | C | T | 4 | a0001c0001t0007g0090 a0001c0001t0008g0141 a0001c0001t0027g0086 others(1): Show |
4 | HG02809.hp1 HG02965.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-16802C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134384830 | |||||||
chr9:134384832 | C | T | 5 | a0001c0001t0004g0225 a0001c0001t0016g0115 a0001c0001t0016g0155 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-16800C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134384832 | |||||||
chr9:134384848 | C | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0049 |
2 | HG00140.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.29-16784C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134384848 | |||||||
chr9:134384897 | G | A | 1 | a0001c0001t0010g0101 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.29-16735G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134384897 | |||||||
chr9:134385017 | T | C | 5 | a0001c0001t0004g0160 a0001c0001t0008g0087 a0001c0001t0026g0127 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-16615T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134385017 | |||||||
chr9:134385213 | A | G | 1 | a0001c0001t0004g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.29-16419A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134385213 | |||||||
chr9:134385319 | C | T | 26 | a0001c0001t0003g0166 a0001c0001t0004g0005 a0001c0001t0004g0153 others(23): Show |
27 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.29-16313C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134385319 | |||||||
chr9:134385371 | G | A | 3 | a0001c0001t0004g0148 a0001c0001t0023g0149 a0001c0001t0023g0150 |
3 | HG02109.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.29-16261G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134385371 | |||||||
chr9:134385467 | C | T | 14 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0081 others(11): Show |
14 | HG00735.hp1 HG01099.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-16165C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134385467 | |||||||
chr9:134385559 | C | T | 36 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0002g0055 others(33): Show |
38 | HG00597.hp2 HG00735.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.29-16073C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134385559 | |||||||
chr9:134385712 | C | T | 1 | a0001c0001t0019g0190 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.29-15920C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134385712 | |||||||
chr9:134385713 | C | T | 1 | a0001c0001t0004g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.29-15919C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134385713 | |||||||
chr9:134385735 | T | A | 1 | a0001c0001t0020g0182 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-15897T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134385735 | |||||||
chr9:134385746 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.29-15886G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134385746 | |||||||
chr9:134385766 | G | A | 2 | a0001c0001t0008g0131 a0001c0001t0041g0139 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.29-15866G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134385766 | |||||||
chr9:134386085 | C | T | 4 | a0001c0001t0008g0087 a0001c0001t0026g0127 a0001c0001t0051g0023 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-15547C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134386085 | |||||||
chr9:134386211 | G | A | 1 | a0001c0001t0005g0200 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.29-15421G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134386211 | |||||||
chr9:134386380 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.29-15252G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134386380 | |||||||
chr9:134386450 | A | G | 6 | a0001c0001t0008g0087 a0001c0001t0026g0127 a0001c0001t0051g0023 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.29-15182A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134386450 | |||||||
chr9:134386548 | T | A | 13 | a0001c0001t0001g0164 a0001c0001t0002g0055 a0001c0001t0002g0081 others(10): Show |
13 | HG00735.hp1 HG01099.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-15084T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134386548 | |||||||
chr9:134386599 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0036g0201 |
2 | HG00642.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.29-15033G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134386599 | |||||||
chr9:134386717 | A | AC | 38 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0005 others(35): Show |
39 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.29-14913dupC | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134386717 | ||||||
chr9:134386736 | TC | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(183): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.29-14890delC | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134386736 | ||||||
chr9:134386871 | G | C | 6 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0001t0006g0002 others(3): Show |
7 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-14761G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134386871 | |||||||
chr9:134387204 | G | A | 21 | a0001c0001t0001g0135 a0001c0001t0004g0005 a0001c0001t0004g0128 others(18): Show |
22 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.29-14428G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134387204 | |||||||
chr9:134387330 | G | A | 1 | a0001c0001t0004g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.29-14302G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134387330 | |||||||
chr9:134387340 | C | T | 1 | a0001c0001t0004g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.29-14292C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134387340 | |||||||
chr9:134387350 | G | A | 1 | a0001c0001t0005g0020 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.29-14282G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134387350 | |||||||
chr9:134387398 | C | T | 4 | a0001c0001t0003g0142 a0001c0001t0007g0108 a0001c0001t0010g0122 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-14234C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134387398 | |||||||
chr9:134387431 | G | C | 1 | a0001c0001t0011g0121 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.29-14201G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134387431 | |||||||
chr9:134387493 | G | C | 1 | a0001c0001t0062g0120 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.29-14139G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134387493 | |||||||
chr9:134387638 | A | T | 1 | a0001c0001t0028g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.29-13994A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134387638 | |||||||
chr9:134387660 | C | T | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.29-13972C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134387660 | |||||||
chr9:134387721 | C | G | 1 | a0001c0001t0001g0036 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.29-13911C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134387721 | |||||||
chr9:134387735 | C | T | 1 | a0001c0001t0008g0125 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.29-13897C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134387735 | |||||||
chr9:134387793 | A | G | 39 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0005 others(36): Show |
40 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.29-13839A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134387793 | |||||||
chr9:134388011 | C | T | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-13621C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134388011 | |||||||
chr9:134388179 | A | ATCCTAGG others(28): Show |
13 | a0001c0001t0002g0052 a0001c0001t0002g0071 a0001c0001t0002g0198 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.29-13431_29-13397d others(37): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134388179 | ||||||
chr9:134388286 | T | TGTGTGTG others(13): Show |
119 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(116): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.29-13339_29-13338i others(22): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134388286 | ||||||
chr9:134388286 | T | TGTGTGTG others(15): Show |
38 | a0001c0001t0001g0022 a0001c0001t0001g0084 a0001c0001t0001g0093 others(35): Show |
39 | HG00621.hp2 HG01109.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.29-13339_29-13338i others(24): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134388286 | ||||||
chr9:134388286 | T | TGTGTGTG others(17): Show |
26 | a0001c0001t0001g0135 a0001c0001t0003g0060 a0001c0001t0004g0128 others(23): Show |
27 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.29-13339_29-13338i others(26): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134388286 | ||||||
chr9:134388286 | T | TGTGTGTG others(19): Show |
4 | a0001c0001t0003g0166 a0001c0001t0008g0037 a0001c0001t0059g0210 others(1): Show |
4 | HG01169.hp2 HG01243.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-13339_29-13338i others(28): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134388286 | ||||||
chr9:134388331 | TGGGGTCA others(4): Show |
T | 1 | a0001c0001t0007g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.29-13297_29-13287d others(13): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134388331 | ||||||
chr9:134388352 | G | T | 3 | a0001c0001t0004g0195 a0001c0001t0060g0100 a0001c0001t0062g0120 |
3 | HG02717.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.29-13280G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134388352 | |||||||
chr9:134388360 | T | C | 94 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0001t0001g0135 others(91): Show |
98 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.29-13272T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134388360 | |||||||
chr9:134388646 | G | T | 12 | a0001c0001t0001g0135 a0001c0001t0004g0128 a0001c0001t0004g0129 others(9): Show |
12 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.29-12986G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134388646 | |||||||
chr9:134388892 | G | T | 1 | a0001c0001t0007g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.29-12740G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134388892 | |||||||
chr9:134388935 | G | A | 21 | a0001c0001t0001g0135 a0001c0001t0004g0005 a0001c0001t0004g0128 others(18): Show |
22 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.29-12697G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134388935 | |||||||
chr9:134388982 | G | A | 2 | a0001c0001t0008g0125 a0001c0001t0022g0208 |
2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.29-12650G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134388982 | |||||||
chr9:134389000 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.29-12632G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389000 | |||||||
chr9:134389021 | G | A | 9 | a0001c0001t0004g0005 a0001c0001t0004g0153 a0001c0001t0004g0160 others(6): Show |
10 | HG02257.hp2 HG02486.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.29-12611G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389021 | |||||||
chr9:134389093 | G | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.29-12539G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389093 | |||||||
chr9:134389143 | C | T | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-12489C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389143 | |||||||
chr9:134389452 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.29-12180G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389452 | |||||||
chr9:134389466 | G | T | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-12166G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389466 | |||||||
chr9:134389503 | C | T | 1 | a0001c0001t0017g0058 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.29-12129C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389503 | |||||||
chr9:134389504 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0009g0098 |
3 | HG01074.hp2 HG01928.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.29-12128G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389504 | |||||||
chr9:134389536 | C | T | 3 | a0001c0001t0004g0195 a0001c0001t0060g0100 a0001c0001t0062g0120 |
3 | HG02717.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.29-12096C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389536 | |||||||
chr9:134389553 | G | A | 39 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0005 others(36): Show |
40 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.29-12079G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389553 | |||||||
chr9:134389555 | G | A | 1 | a0001c0001t0004g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.29-12077G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389555 | |||||||
chr9:134389563 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.29-12069T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389563 | |||||||
chr9:134389737 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.29-11895G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389737 | |||||||
chr9:134389861 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0107 |
3 | HG01074.hp2 HG01928.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.29-11771C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134389861 | |||||||
chr9:134390090 | G | A | 3 | a0001c0001t0008g0087 a0001c0001t0026g0127 a0001c0004t0005g0126 |
3 | HG02717.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.29-11542G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134390090 | |||||||
chr9:134390144 | T | A | 10 | a0001c0001t0008g0125 a0001c0001t0009g0157 a0001c0001t0010g0101 others(7): Show |
10 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.29-11488T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134390144 | |||||||
chr9:134390237 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.29-11395C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134390237 | |||||||
chr9:134390456 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(96): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.29-11176C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134390456 | |||||||
chr9:134390666 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.29-10966C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134390666 | |||||||
chr9:134390937 | C | T | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.29-10695C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134390937 | |||||||
chr9:134391038 | C | G | 1 | a0001c0001t0001g0066 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.29-10594C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134391038 | |||||||
chr9:134391038 | C | T | 3 | a0001c0001t0004g0133 a0001c0001t0007g0119 a0001c0001t0007g0203 |
3 | HG02258.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.29-10594C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134391038 | |||||||
chr9:134391162 | A | C | 39 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0005 others(36): Show |
40 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.29-10470A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134391162 | |||||||
chr9:134391233 | A | G | 39 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0005 others(36): Show |
40 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.29-10399A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134391233 | |||||||
chr9:134391302 | C | T | 39 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0005 others(36): Show |
40 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.29-10330C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134391302 | |||||||
chr9:134391354 | G | A | 4 | a0001c0001t0003g0166 a0001c0001t0008g0037 a0001c0001t0056g0143 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-10278G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134391354 | |||||||
chr9:134391551 | A | G | 1 | a0001c0001t0054g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.29-10081A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134391551 | |||||||
chr9:134391740 | T | C | 39 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0005 others(36): Show |
40 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.29-9892T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134391740 | |||||||
chr9:134391741 | G | A | 39 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0005 others(36): Show |
40 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.29-9891G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134391741 | |||||||
chr9:134392200 | C | T | 1 | a0001c0001t0009g0138 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.29-9432C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134392200 | |||||||
chr9:134392230 | G | A | 39 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0005 others(36): Show |
40 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.29-9402G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134392230 | |||||||
chr9:134392230 | G | T | 4 | a0001c0001t0002g0055 a0001c0001t0002g0081 a0001c0001t0057g0053 others(1): Show |
4 | HG01099.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-9402G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134392230 | |||||||
chr9:134392340 | C | G | 4 | a0001c0001t0003g0166 a0001c0001t0008g0037 a0001c0001t0056g0143 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-9292C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134392340 | |||||||
chr9:134392407 | C | T | 1 | a0001c0001t0002g0179 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.29-9225C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134392407 | |||||||
chr9:134392535 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(89): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.29-9097C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134392535 | |||||||
chr9:134392788 | T | A | 3 | a0001c0001t0004g0133 a0001c0001t0007g0119 a0001c0001t0007g0203 |
3 | HG02258.hp2 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.29-8844T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134392788 | |||||||
chr9:134392795 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.29-8837G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134392795 | |||||||
chr9:134393025 | T | TA | 120 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(117): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.29-8595dupA | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134393025 | ||||||
chr9:134393077 | G | A | 4 | a0001c0001t0003g0142 a0001c0001t0007g0108 a0001c0001t0010g0122 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-8555G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393077 | |||||||
chr9:134393115 | C | A | 1 | a0001c0001t0014g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.29-8517C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393115 | |||||||
chr9:134393141 | G | A | 1 | a0001c0001t0004g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.29-8491G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393141 | |||||||
chr9:134393237 | CAG | C | 21 | a0001c0001t0002g0001 a0001c0001t0002g0052 a0001c0001t0002g0071 others(18): Show |
23 | HG00408.hp1 HG00597.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.29-8394_29-8393del others(2): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393237 | |||||||
chr9:134393263 | A | T | 20 | a0001c0001t0001g0135 a0001c0001t0004g0005 a0001c0001t0004g0128 others(17): Show |
21 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.29-8369A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393263 | |||||||
chr9:134393314 | C | T | 4 | a0001c0001t0003g0142 a0001c0001t0007g0108 a0001c0001t0010g0122 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-8318C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393314 | |||||||
chr9:134393409 | T | G | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-8223T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393409 | |||||||
chr9:134393432 | C | T | 14 | a0001c0001t0002g0052 a0001c0001t0002g0071 a0001c0001t0002g0198 others(11): Show |
14 | HG00408.hp1 HG00597.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.29-8200C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393432 | |||||||
chr9:134393475 | G | A | 6 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(3): Show |
6 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-8157G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393475 | |||||||
chr9:134393489 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.29-8143G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393489 | |||||||
chr9:134393631 | G | A | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-8001G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393631 | |||||||
chr9:134393657 | A | G | 188 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(185): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.29-7975A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393657 | |||||||
chr9:134393946 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.29-7686C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134393946 | |||||||
chr9:134394106 | C | T | 1 | a0001c0001t0004g0202 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.29-7526C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134394106 | |||||||
chr9:134394154 | G | GGTGATGG others(1028): Show |
1 | a0001c0001t0014g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.29-7466_29-7465ins others(1035): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1013): Show |
4 | a0001c0001t0008g0087 a0001c0001t0026g0127 a0001c0001t0051g0023 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1020): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1022): Show |
1 | a0001c0001t0018g0104 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.29-7466_29-7465ins others(1029): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(998): Show |
1 | a0001c0001t0060g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.29-7466_29-7465ins others(1005): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(993): Show |
2 | a0001c0001t0008g0131 a0001c0001t0041g0139 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1000): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1001): Show |
1 | a0001c0001t0011g0132 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.29-7466_29-7465ins others(1008): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1001): Show |
2 | a0001c0001t0004g0195 a0001c0001t0062g0120 |
2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1008): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1004): Show |
10 | a0001c0001t0001g0135 a0001c0001t0004g0128 a0001c0001t0004g0129 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1011): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1001): Show |
8 | a0001c0001t0004g0005 a0001c0001t0004g0153 a0001c0001t0004g0160 others(5): Show |
9 | HG02257.hp2 HG02486.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1008): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(996): Show |
15 | a0001c0001t0003g0080 a0001c0001t0008g0125 a0001c0001t0009g0098 others(12): Show |
15 | HG00735.hp1 HG01109.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1003): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1019): Show |
4 | a0001c0001t0003g0142 a0001c0001t0007g0108 a0001c0001t0010g0122 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1026): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1022): Show |
5 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0107 others(2): Show |
5 | HG01074.hp2 HG01928.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1029): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1025): Show |
80 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0016 others(77): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1032): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1019): Show |
6 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(3): Show |
6 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1026): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1025): Show |
1 | a0001c0001t0002g0029 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.29-7466_29-7465ins others(1032): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1025): Show |
42 | a0001c0001t0001g0046 a0001c0001t0001g0078 a0001c0001t0001g0079 others(39): Show |
43 | HG00597.hp1 HG00621.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1032): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1022): Show |
1 | a0001c0001t0032g0017 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.29-7466_29-7465ins others(1029): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1025): Show |
19 | a0001c0001t0002g0001 a0001c0001t0002g0052 a0001c0001t0002g0071 others(16): Show |
21 | HG00408.hp1 HG00597.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1032): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1022): Show |
1 | a0001c0001t0004g0204 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.29-7466_29-7465ins others(1029): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1025): Show |
5 | a0001c0001t0001g0194 a0001c0001t0006g0021 a0001c0001t0006g0181 others(2): Show |
5 | HG00642.hp2 HG01099.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1032): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1025): Show |
4 | a0001c0001t0002g0055 a0001c0001t0002g0081 a0001c0001t0057g0053 others(1): Show |
4 | HG01099.hp2 HG01255.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1032): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1025): Show |
4 | a0001c0001t0004g0148 a0001c0001t0004g0209 a0001c0001t0023g0149 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1032): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1001): Show |
2 | a0001c0001t0013g0188 a0001c0001t0013g0197 |
2 | NA18947.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1008): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394154 | G | GGTGATGG others(1001): Show |
4 | a0001c0001t0003g0166 a0001c0001t0008g0037 a0001c0001t0056g0143 others(1): Show |
4 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-7466_29-7465ins others(1008): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394154 | ||||||
chr9:134394167 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0007g0090 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.29-7465A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134394167 | |||||||
chr9:134394179 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0007g0090 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.29-7453A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134394179 | |||||||
chr9:134394184 | G | GGTGATGG others(1024): Show |
2 | a0001c0001t0001g0164 a0001c0001t0007g0090 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.29-7448_29-7447ins others(1031): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134394184 | |||||||
chr9:134394185 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0007g0090 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.29-7447A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134394185 | |||||||
chr9:134394246 | C | T | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-7386C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134394246 | |||||||
chr9:134394254 | A | G | 4 | a0001c0001t0008g0087 a0001c0001t0026g0127 a0001c0001t0051g0023 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-7378A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134394254 | |||||||
chr9:134394261 | C | T | 24 | a0001c0001t0001g0135 a0001c0001t0002g0110 a0001c0001t0002g0111 others(21): Show |
25 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.29-7371C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134394261 | |||||||
chr9:134394560 | A | G | 20 | a0001c0001t0001g0135 a0001c0001t0004g0005 a0001c0001t0004g0128 others(17): Show |
21 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.29-7072A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134394560 | |||||||
chr9:134394750 | C | A | 4 | a0001c0001t0003g0142 a0001c0001t0007g0108 a0001c0001t0010g0122 others(1): Show |
4 | HG01891.hp2 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-6882C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134394750 | |||||||
chr9:134394899 | G | A | 6 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(3): Show |
6 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-6733G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134394899 | |||||||
chr9:134394905 | G | GC | 6 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(3): Show |
6 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-6726dupC | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 134394905 | ||||||
chr9:134394906 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.29-6726C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134394906 | |||||||
chr9:134395187 | C | T | 6 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(3): Show |
6 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-6445C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134395187 | |||||||
chr9:134395209 | G | A | 2 | a0001c0001t0003g0166 a0001c0001t0008g0037 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.29-6423G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134395209 | |||||||
chr9:134395311 | G | T | 26 | a0001c0001t0001g0194 a0001c0001t0002g0001 a0001c0001t0002g0052 others(23): Show |
28 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.29-6321G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134395311 | |||||||
chr9:134395579 | A | G | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-6053A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134395579 | |||||||
chr9:134395724 | A | G | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-5908A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134395724 | |||||||
chr9:134395738 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.29-5894C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134395738 | |||||||
chr9:134395783 | T | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(79): Show |
83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.29-5849T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134395783 | |||||||
chr9:134396014 | T | C | 86 | a0001c0001t0001g0135 a0001c0001t0001g0194 a0001c0001t0002g0001 others(83): Show |
89 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.29-5618T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396014 | |||||||
chr9:134396028 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.29-5604G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396028 | |||||||
chr9:134396067 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(75): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.29-5565C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396067 | |||||||
chr9:134396086 | C | G | 1 | a0001c0001t0053g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.29-5546C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396086 | |||||||
chr9:134396113 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.29-5519G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396113 | |||||||
chr9:134396181 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0088 |
2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.29-5451A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396181 | |||||||
chr9:134396363 | C | T | 3 | a0001c0001t0002g0111 a0001c0001t0003g0222 a0001c0001t0003g0224 |
3 | HG00738.hp2 HG01243.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.29-5269C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396363 | |||||||
chr9:134396388 | G | A | 1 | a0001c0001t0022g0208 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.29-5244G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396388 | |||||||
chr9:134396517 | G | A | 1 | a0001c0001t0017g0057 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.29-5115G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396517 | |||||||
chr9:134396594 | A | G | 13 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0128 others(10): Show |
13 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-5038A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396594 | |||||||
chr9:134396636 | C | T | 2 | a0001c0001t0005g0147 a0001c0001t0009g0130 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.29-4996C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396636 | |||||||
chr9:134396654 | C | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.29-4978C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396654 | |||||||
chr9:134396739 | C | T | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-4893C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396739 | |||||||
chr9:134396742 | C | T | 1 | a0001c0001t0005g0020 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.29-4890C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396742 | |||||||
chr9:134396782 | A | G | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-4850A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396782 | |||||||
chr9:134396793 | G | A | 1 | a0001c0001t0014g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.29-4839G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396793 | |||||||
chr9:134396900 | T | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.29-4732T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396900 | |||||||
chr9:134396936 | G | A | 87 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(84): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.29-4696G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134396936 | |||||||
chr9:134397245 | G | C | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-4387G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397245 | |||||||
chr9:134397264 | C | T | 2 | a0001c0001t0023g0149 a0001c0001t0023g0150 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.29-4368C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397264 | |||||||
chr9:134397280 | G | A | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-4352G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397280 | |||||||
chr9:134397310 | T | G | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-4322T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397310 | |||||||
chr9:134397348 | C | T | 1 | a0001c0001t0002g0196 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.29-4284C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397348 | |||||||
chr9:134397380 | G | A | 4 | a0001c0001t0008g0087 a0001c0001t0026g0127 a0001c0001t0051g0023 others(1): Show |
4 | HG02717.hp2 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-4252G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397380 | |||||||
chr9:134397662 | G | T | 24 | a0001c0001t0001g0135 a0001c0001t0003g0166 a0001c0001t0004g0005 others(21): Show |
25 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.29-3970G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397662 | |||||||
chr9:134397784 | C | T | 2 | a0001c0001t0050g0042 a0001c0001t0061g0156 |
2 | HG03225.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.29-3848C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397784 | |||||||
chr9:134397799 | C | T | 3 | a0001c0001t0004g0195 a0001c0001t0060g0100 a0001c0001t0062g0120 |
3 | HG02717.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.29-3833C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397799 | |||||||
chr9:134397867 | C | T | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.29-3765C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397867 | |||||||
chr9:134397880 | G | T | 1 | a0001c0001t0005g0176 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.29-3752G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397880 | |||||||
chr9:134397899 | G | T | 3 | a0001c0001t0003g0142 a0001c0001t0010g0122 a0001c0001t0011g0121 |
3 | HG01891.hp2 HG02145.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.29-3733G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397899 | |||||||
chr9:134397985 | T | A | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-3647T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397985 | |||||||
chr9:134397986 | A | T | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-3646A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134397986 | |||||||
chr9:134398271 | T | C | 188 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(185): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.29-3361T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134398271 | |||||||
chr9:134398314 | T | G | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-3318T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134398314 | |||||||
chr9:134398374 | C | CGCACGTG others(1): Show |
186 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(183): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.29-3258_29-3257ins others(8): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134398374 | |||||||
chr9:134398444 | C | T | 1 | a0001c0001t0049g0041 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.29-3188C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134398444 | |||||||
chr9:134398564 | A | G | 186 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(183): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.29-3068A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134398564 | |||||||
chr9:134398764 | T | G | 1 | a0001c0001t0021g0106 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.29-2868T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134398764 | |||||||
chr9:134398773 | G | A | 1 | a0001c0001t0008g0037 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.29-2859G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134398773 | |||||||
chr9:134398853 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.29-2779A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134398853 | |||||||
chr9:134398879 | G | T | 38 | a0001c0001t0001g0194 a0001c0001t0002g0001 a0001c0001t0002g0052 others(35): Show |
40 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.29-2753G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134398879 | |||||||
chr9:134398902 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.29-2730T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134398902 | |||||||
chr9:134398922 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0001t0005g0147 others(5): Show |
9 | HG00621.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.29-2710G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134398922 | |||||||
chr9:134398994 | T | C | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-2638T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134398994 | |||||||
chr9:134399142 | C | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0064 others(4): Show |
7 | HG01346.hp2 HG02486.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-2490C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134399142 | |||||||
chr9:134399242 | G | A | 3 | a0001c0001t0004g0195 a0001c0001t0060g0100 a0001c0001t0062g0120 |
3 | HG02717.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.29-2390G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134399242 | |||||||
chr9:134399523 | G | C | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-2109G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134399523 | |||||||
chr9:134399565 | T | TCA | 6 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(3): Show |
6 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-2067_29-2066ins others(2): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134399565 | |||||||
chr9:134399571 | C | T | 2 | a0001c0001t0023g0149 a0001c0001t0023g0150 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.29-2061C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134399571 | |||||||
chr9:134399724 | T | C | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-1908T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134399724 | |||||||
chr9:134399787 | G | A | 3 | a0001c0001t0008g0087 a0001c0001t0026g0127 a0001c0004t0005g0126 |
3 | HG02717.hp2 HG02976.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.29-1845G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134399787 | |||||||
chr9:134399894 | C | T | 26 | a0001c0001t0001g0194 a0001c0001t0002g0001 a0001c0001t0002g0052 others(23): Show |
28 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.29-1738C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134399894 | |||||||
chr9:134400068 | G | A | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-1564G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400068 | |||||||
chr9:134400108 | C | T | 1 | a0001c0001t0007g0035 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.29-1524C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400108 | |||||||
chr9:134400110 | A | G | 1 | a0001c0001t0007g0108 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.29-1522A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400110 | |||||||
chr9:134400180 | C | G | 2 | a0001c0001t0013g0188 a0001c0001t0013g0197 |
2 | NA18947.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.29-1452C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400180 | |||||||
chr9:134400240 | C | G | 17 | a0001c0001t0003g0080 a0001c0001t0008g0125 a0001c0001t0008g0131 others(14): Show |
17 | HG00735.hp1 HG01109.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.29-1392C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400240 | |||||||
chr9:134400241 | C | T | 1 | a0001c0001t0053g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.29-1391C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400241 | |||||||
chr9:134400255 | G | T | 2 | a0001c0001t0018g0104 a0001c0001t0018g0105 |
2 | NA18944.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.29-1377G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400255 | |||||||
chr9:134400306 | G | A | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-1326G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400306 | |||||||
chr9:134400310 | G | T | 82 | a0001c0001t0001g0135 a0001c0001t0001g0194 a0001c0001t0002g0001 others(79): Show |
85 | HG00408.hp1 HG00597.hp2 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.29-1322G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400310 | |||||||
chr9:134400321 | A | G | 8 | a0001c0001t0002g0055 a0001c0001t0002g0081 a0001c0001t0004g0148 others(5): Show |
8 | HG01099.hp2 HG01255.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.29-1311A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400321 | |||||||
chr9:134400659 | T | C | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-973T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400659 | |||||||
chr9:134400695 | A | G | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-937A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400695 | |||||||
chr9:134400699 | C | T | 3 | a0001c0001t0011g0132 a0001c0001t0014g0173 a0001c0001t0024g0172 |
3 | HG01884.hp2 HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.29-933C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400699 | |||||||
chr9:134400927 | G | A | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-705G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400927 | |||||||
chr9:134400999 | C | T | 1 | a0001c0001t0038g0074 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.29-633C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134400999 | |||||||
chr9:134401026 | C | T | 4 | a0001c0001t0004g0133 a0001c0001t0004g0202 a0001c0001t0007g0119 others(1): Show |
4 | HG00735.hp2 HG02258.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-606C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134401026 | |||||||
chr9:134401038 | C | T | 1 | a0001c0001t0006g0177 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.29-594C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134401038 | |||||||
chr9:134401049 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.29-583G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134401049 | |||||||
chr9:134401116 | T | C | 44 | a0001c0001t0001g0135 a0001c0001t0003g0080 a0001c0001t0003g0166 others(41): Show |
45 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.29-516T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134401116 | |||||||
chr9:134401184 | G | A | 1 | a0001c0001t0045g0161 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.29-448G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134401184 | |||||||
chr9:134401368 | C | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0075 a0001c0001t0001g0113 others(6): Show |
9 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.29-264C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134401368 | |||||||
chr9:134401396 | G | A | 1 | a0001c0001t0003g0080 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.29-236G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134401396 | |||||||
chr9:134401399 | C | T | 3 | a0001c0001t0004g0195 a0001c0001t0060g0100 a0001c0001t0062g0120 |
3 | HG02717.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.29-233C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134401399 | |||||||
chr9:134401481 | G | A | 2 | a0001c0001t0005g0147 a0001c0001t0009g0130 |
2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.29-151G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 1/9 | chr9 | 134401481 | |||||||
chr9:134401915 | G | A | 165 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0016 others(162): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.279+33G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134401915 | |||||||
chr9:134401996 | C | G | 3 | a0001c0001t0006g0021 a0001c0001t0006g0181 a0001c0001t0014g0180 |
3 | HG01099.hp1 HG01256.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.279+114C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134401996 | |||||||
chr9:134402035 | A | C | 39 | a0001c0001t0001g0135 a0001c0001t0002g0001 a0001c0001t0003g0080 others(36): Show |
42 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.279+153A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402035 | |||||||
chr9:134402039 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.279+157C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402039 | |||||||
chr9:134402147 | C | T | 1 | a0001c0001t0008g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.279+265C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402147 | |||||||
chr9:134402157 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.279+275G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402157 | |||||||
chr9:134402184 | A | G | 181 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(178): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.279+302A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402184 | |||||||
chr9:134402265 | C | A | 3 | a0001c0001t0005g0147 a0001c0001t0009g0130 a0001c0001t0011g0132 |
3 | HG01884.hp2 HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.279+383C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402265 | |||||||
chr9:134402354 | C | T | 2 | a0001c0001t0008g0131 a0001c0001t0041g0139 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.279+472C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402354 | |||||||
chr9:134402382 | T | A | 6 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(3): Show |
6 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+500T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402382 | |||||||
chr9:134402389 | G | A | 1 | a0001c0001t0021g0106 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.279+507G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402389 | |||||||
chr9:134402645 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.279+763G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402645 | |||||||
chr9:134402679 | AG | A | 23 | a0001c0001t0001g0135 a0001c0001t0004g0005 a0001c0001t0004g0128 others(20): Show |
24 | HG01943.hp2 HG02055.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.279+800delG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 134402679 | ||||||
chr9:134402854 | G | A | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.279+972G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402854 | |||||||
chr9:134402856 | T | C | 39 | a0001c0001t0001g0135 a0001c0001t0002g0001 a0001c0001t0003g0080 others(36): Show |
42 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.279+974T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402856 | |||||||
chr9:134402891 | TG | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(79): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.279+1010delG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402891 | |||||||
chr9:134402908 | C | G | 1 | a0001c0001t0002g0052 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.279+1026C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134402908 | |||||||
chr9:134403056 | C | T | 2 | a0001c0001t0008g0087 a0001c0001t0051g0023 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.279+1174C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403056 | |||||||
chr9:134403133 | G | C | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.279+1251G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403133 | |||||||
chr9:134403170 | G | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0068 a0001c0001t0001g0083 |
4 | NA18944.hp1 NA18954.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+1288G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403170 | |||||||
chr9:134403254 | A | G | 39 | a0001c0001t0001g0135 a0001c0001t0002g0001 a0001c0001t0003g0080 others(36): Show |
42 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.279+1372A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403254 | |||||||
chr9:134403436 | T | C | 39 | a0001c0001t0001g0135 a0001c0001t0002g0001 a0001c0001t0003g0080 others(36): Show |
42 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.279+1554T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403436 | |||||||
chr9:134403458 | G | A | 60 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0016 others(57): Show |
62 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(59): Show |
intron_variant | MODIFIER | c.279+1576G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403458 | |||||||
chr9:134403478 | C | T | 1 | a0001c0001t0011g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.279+1596C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403478 | |||||||
chr9:134403491 | G | C | 40 | a0001c0001t0001g0135 a0001c0001t0002g0001 a0001c0001t0003g0080 others(37): Show |
43 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.279+1609G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403491 | |||||||
chr9:134403557 | C | T | 1 | a0001c0001t0049g0041 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.279+1675C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403557 | |||||||
chr9:134403558 | G | T | 6 | a0001c0001t0004g0153 a0001c0001t0010g0213 a0001c0001t0016g0207 others(3): Show |
6 | HG02257.hp2 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.279+1676G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403558 | |||||||
chr9:134403607 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.279+1725G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403607 | |||||||
chr9:134403639 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(158): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.279+1757A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403639 | |||||||
chr9:134403644 | T | C | 2 | a0001c0001t0008g0087 a0001c0001t0010g0122 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.279+1762T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403644 | |||||||
chr9:134403858 | G | A | 1 | a0001c0001t0044g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.279+1976G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403858 | |||||||
chr9:134403874 | G | T | 1 | a0001c0001t0008g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.279+1992G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403874 | |||||||
chr9:134403893 | C | T | 5 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(2): Show |
5 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+2011C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403893 | |||||||
chr9:134403900 | T | C | 6 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(3): Show |
6 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+2018T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403900 | |||||||
chr9:134403910 | G | T | 1 | a0001c0001t0023g0150 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.279+2028G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134403910 | |||||||
chr9:134404040 | A | G | 6 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(3): Show |
6 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.279+2158A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134404040 | |||||||
chr9:134404115 | C | G | 5 | a0001c0001t0004g0225 a0001c0001t0016g0115 a0001c0001t0016g0155 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.279+2233C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134404115 | |||||||
chr9:134404236 | A | G | 1 | a0001c0001t0003g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.279+2354A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134404236 | |||||||
chr9:134404252 | A | G | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.279+2370A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134404252 | |||||||
chr9:134404264 | G | A | 3 | a0001c0001t0004g0148 a0001c0001t0023g0149 a0001c0001t0023g0150 |
3 | HG02109.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.279+2382G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134404264 | |||||||
chr9:134404344 | C | A | 1 | a0001c0001t0041g0139 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.279+2462C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134404344 | |||||||
chr9:134404374 | C | G | 3 | a0001c0001t0009g0137 a0001c0001t0009g0138 a0001c0001t0044g0136 |
3 | HG02647.hp2 HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.279+2492C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134404374 | |||||||
chr9:134404401 | C | G | 1 | a0001c0001t0003g0080 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.279+2519C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134404401 | |||||||
chr9:134404414 | G | A | 4 | a0001c0001t0004g0204 a0001c0001t0009g0137 a0001c0001t0009g0138 others(1): Show |
4 | HG02647.hp2 HG03453.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+2532G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134404414 | |||||||
chr9:134404664 | G | A | 1 | a0001c0001t0046g0152 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.279+2782G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134404664 | |||||||
chr9:134405046 | G | A | 8 | a0001c0001t0001g0194 a0001c0001t0004g0205 a0001c0001t0006g0021 others(5): Show |
8 | HG00642.hp2 HG01099.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.280-3103G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405046 | |||||||
chr9:134405130 | C | A | 8 | a0001c0001t0001g0164 a0001c0001t0007g0119 a0001c0001t0007g0203 others(5): Show |
8 | HG02258.hp2 HG02723.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.280-3019C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405130 | |||||||
chr9:134405142 | G | A | 10 | a0001c0001t0001g0164 a0001c0001t0007g0119 a0001c0001t0007g0203 others(7): Show |
10 | HG02258.hp2 HG02723.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.280-3007G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405142 | |||||||
chr9:134405209 | C | T | 18 | a0001c0001t0001g0194 a0001c0001t0004g0133 a0001c0001t0004g0202 others(15): Show |
18 | HG00642.hp2 HG00735.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.280-2940C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405209 | |||||||
chr9:134405260 | C | T | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.280-2889C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405260 | |||||||
chr9:134405332 | C | G | 1 | a0001c0001t0016g0207 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280-2817C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405332 | |||||||
chr9:134405367 | C | T | 1 | a0001c0001t0013g0197 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.280-2782C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405367 | |||||||
chr9:134405381 | A | G | 17 | a0001c0001t0001g0217 a0001c0001t0002g0001 a0001c0001t0005g0004 others(14): Show |
19 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.280-2768A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405381 | |||||||
chr9:134405384 | G | A | 39 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(36): Show |
40 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.280-2765G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405384 | |||||||
chr9:134405391 | C | G | 3 | a0001c0001t0006g0002 a0001c0001t0035g0007 a0001c0002t0002g0008 |
4 | HG01070.hp1 HG01071.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-2758C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405391 | |||||||
chr9:134405512 | G | A | 4 | a0001c0001t0007g0090 a0001c0001t0007g0108 a0001c0001t0032g0017 others(1): Show |
4 | HG01255.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-2637G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405512 | |||||||
chr9:134405553 | G | C | 1 | a0001c0001t0005g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.280-2596G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405553 | |||||||
chr9:134405582 | G | T | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.280-2567G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405582 | |||||||
chr9:134405600 | C | T | 3 | a0001c0001t0009g0130 a0001c0001t0009g0137 a0001c0001t0009g0138 |
3 | HG02647.hp2 HG02818.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.280-2549C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405600 | |||||||
chr9:134405691 | G | A | 4 | a0001c0001t0004g0225 a0001c0001t0016g0115 a0001c0001t0016g0155 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.280-2458G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405691 | |||||||
chr9:134405761 | C | T | 1 | a0001c0001t0060g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.280-2388C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405761 | |||||||
chr9:134405881 | C | G | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.280-2268C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134405881 | |||||||
chr9:134406250 | T | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(88): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.280-1899T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134406250 | |||||||
chr9:134406310 | A | G | 1 | a0001c0001t0002g0198 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.280-1839A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134406310 | |||||||
chr9:134406314 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.280-1835G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134406314 | |||||||
chr9:134406394 | G | GA | 25 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0008g0141 others(22): Show |
25 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.280-1735dupA | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 134406394 | ||||||
chr9:134406394 | GA | G | 25 | a0001c0001t0001g0079 a0001c0001t0001g0217 a0001c0001t0002g0001 others(22): Show |
27 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.280-1735delA | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 134406394 | ||||||
chr9:134406413 | A | G | 1 | a0001c0001t0057g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.280-1736A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134406413 | |||||||
chr9:134406474 | C | T | 5 | a0001c0001t0004g0225 a0001c0001t0008g0141 a0001c0001t0016g0115 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.280-1675C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134406474 | |||||||
chr9:134406475 | A | G | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.280-1674A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134406475 | |||||||
chr9:134406568 | C | T | 20 | a0001c0001t0004g0005 a0001c0001t0004g0128 a0001c0001t0004g0129 others(17): Show |
21 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.280-1581C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134406568 | |||||||
chr9:134406572 | C | T | 17 | a0001c0001t0004g0005 a0001c0001t0004g0128 a0001c0001t0004g0129 others(14): Show |
18 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.280-1577C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134406572 | |||||||
chr9:134406769 | C | T | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.280-1380C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134406769 | |||||||
chr9:134406853 | T | G | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.280-1296T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134406853 | |||||||
chr9:134406969 | C | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(173): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.280-1180C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134406969 | |||||||
chr9:134407073 | T | C | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.280-1076T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134407073 | |||||||
chr9:134407118 | A | G | 11 | a0001c0001t0004g0225 a0001c0001t0008g0141 a0001c0001t0009g0098 others(8): Show |
11 | HG02615.hp2 HG02647.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.280-1031A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134407118 | |||||||
chr9:134407131 | C | T | 8 | a0001c0001t0009g0157 a0001c0001t0010g0163 a0001c0001t0012g0038 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.280-1018C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134407131 | |||||||
chr9:134407366 | A | G | 180 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(177): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.280-783A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134407366 | |||||||
chr9:134407394 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.280-755C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134407394 | |||||||
chr9:134407513 | C | T | 2 | a0001c0001t0039g0206 a0001c0001t0061g0156 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.280-636C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134407513 | |||||||
chr9:134407531 | C | G | 1 | a0001c0001t0002g0196 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.280-618C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134407531 | |||||||
chr9:134407670 | T | TG | 17 | a0001c0001t0004g0225 a0001c0001t0008g0141 a0001c0001t0009g0098 others(14): Show |
17 | HG02258.hp1 HG02486.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.280-472dupG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 134407670 | ||||||
chr9:134407797 | A | G | 1 | a0001c0001t0002g0029 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.280-352A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134407797 | |||||||
chr9:134407944 | A | G | 10 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0036 others(7): Show |
10 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(7): Show |
intron_variant | MODIFIER | c.280-205A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134407944 | |||||||
chr9:134407983 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.280-166C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134407983 | |||||||
chr9:134407991 | C | T | 1 | a0001c0001t0060g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.280-158C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134407991 | |||||||
chr9:134408004 | C | T | 1 | a0001c0001t0014g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.280-145C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134408004 | |||||||
chr9:134408016 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01928.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.280-133A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134408016 | |||||||
chr9:134408066 | C | T | 5 | a0001c0001t0002g0055 a0001c0001t0002g0081 a0001c0001t0057g0053 others(2): Show |
5 | HG01099.hp2 HG01169.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.280-83C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134408066 | |||||||
chr9:134408103 | C | A | 92 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(89): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.280-46C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | chr9 | 134408103 | |||||||
chr9:134408138 | GC | G | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
splice_region_variant&intron_variant | LOW | c.280-3delC | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 134408138 | ||||||
chr9:134408460 | C | T | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.430+161C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 3/9 | chr9 | 134408460 | |||||||
chr9:134408482 | C | T | 10 | a0001c0001t0004g0225 a0001c0001t0008g0141 a0001c0001t0009g0098 others(7): Show |
10 | HG02615.hp2 HG02647.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.430+183C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 3/9 | chr9 | 134408482 | |||||||
chr9:134408667 | C | G | 1 | a0001c0001t0003g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.431-273C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 3/9 | chr9 | 134408667 | |||||||
chr9:134408752 | T | C | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.431-188T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 3/9 | chr9 | 134408752 | |||||||
chr9:134408879 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.431-61G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 3/9 | chr9 | 134408879 | |||||||
chr9:134408896 | G | A | 2 | a0001c0001t0009g0130 a0001c0001t0009g0138 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.431-44G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 3/9 | chr9 | 134408896 | |||||||
chr9:134409174 | C | T | 1 | a0001c0001t0052g0012 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.610+55C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134409174 | |||||||
chr9:134409271 | CGCGTGGG others(17): Show |
C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.610+165_610+188del others(24): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 134409271 | ||||||
chr9:134409348 | C | T | 6 | a0001c0001t0003g0060 a0001c0001t0003g0069 a0001c0001t0019g0059 others(3): Show |
6 | HG01069.hp2 HG01074.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.610+229C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134409348 | |||||||
chr9:134409407 | C | T | 5 | a0001c0001t0003g0142 a0001c0001t0004g0148 a0001c0001t0004g0209 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.610+288C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134409407 | |||||||
chr9:134409412 | G | A | 1 | a0001c0001t0047g0116 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.610+293G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134409412 | |||||||
chr9:134409416 | C | A | 14 | a0001c0001t0001g0194 a0001c0001t0006g0021 a0001c0001t0009g0157 others(11): Show |
14 | HG00642.hp2 HG01099.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.610+297C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134409416 | |||||||
chr9:134409463 | C | T | 2 | a0001c0001t0007g0119 a0001c0001t0007g0203 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.610+344C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134409463 | |||||||
chr9:134409808 | G | A | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.610+689G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134409808 | |||||||
chr9:134409815 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.610+696C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134409815 | |||||||
chr9:134410009 | A | T | 2 | a0001c0001t0001g0175 a0001c0001t0003g0025 |
2 | NA18969.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.610+890A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134410009 | |||||||
chr9:134410020 | A | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(181): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.610+901A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134410020 | |||||||
chr9:134410046 | C | G | 2 | a0001c0001t0017g0057 a0001c0001t0017g0058 |
2 | HG00621.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.610+927C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134410046 | |||||||
chr9:134410058 | C | T | 8 | a0001c0001t0009g0157 a0001c0001t0010g0163 a0001c0001t0012g0038 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.610+939C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134410058 | |||||||
chr9:134410118 | C | G | 1 | a0001c0001t0005g0144 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.610+999C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134410118 | |||||||
chr9:134410150 | C | T | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.610+1031C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134410150 | |||||||
chr9:134410165 | T | C | 5 | a0001c0001t0003g0142 a0001c0001t0004g0148 a0001c0001t0004g0209 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.610+1046T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134410165 | |||||||
chr9:134410301 | G | A | 1 | a0001c0001t0004g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.610+1182G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134410301 | |||||||
chr9:134410366 | G | T | 14 | a0001c0001t0001g0194 a0001c0001t0006g0021 a0001c0001t0009g0157 others(11): Show |
14 | HG00642.hp2 HG01099.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.610+1247G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134410366 | |||||||
chr9:134410706 | T | TG | 39 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(36): Show |
40 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.610+1595dupG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 134410706 | ||||||
chr9:134410763 | A | G | 5 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(2): Show |
5 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.610+1644A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134410763 | |||||||
chr9:134410785 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.610+1666C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134410785 | |||||||
chr9:134411010 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.610+1891C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134411010 | |||||||
chr9:134411149 | G | C | 22 | a0001c0001t0004g0005 a0001c0001t0004g0128 a0001c0001t0004g0129 others(19): Show |
23 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.610+2030G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134411149 | |||||||
chr9:134411195 | G | A | 2 | a0001c0001t0005g0144 a0001c0001t0005g0200 |
2 | HG02040.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.610+2076G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134411195 | |||||||
chr9:134411263 | G | C | 2 | a0001c0001t0004g0133 a0001c0001t0004g0202 |
2 | HG00735.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.610+2144G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134411263 | |||||||
chr9:134411331 | GA | G | 83 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(80): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.610+2213delA | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134411331 | |||||||
chr9:134411518 | G | A | 5 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(2): Show |
5 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.610+2399G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134411518 | |||||||
chr9:134411717 | C | T | 6 | a0001c0001t0007g0119 a0001c0001t0007g0203 a0001c0001t0008g0131 others(3): Show |
6 | HG02258.hp2 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.610+2598C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134411717 | |||||||
chr9:134411837 | G | C | 6 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0056 others(3): Show |
6 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.610+2718G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134411837 | |||||||
chr9:134411871 | G | C | 4 | a0001c0001t0008g0125 a0001c0001t0011g0121 a0001c0001t0016g0207 others(1): Show |
4 | HG01891.hp2 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.610+2752G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134411871 | |||||||
chr9:134412002 | T | C | 1 | a0001c0001t0034g0011 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.610+2883T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134412002 | |||||||
chr9:134412120 | G | A | 1 | a0001c0001t0005g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.610+3001G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134412120 | |||||||
chr9:134412174 | G | T | 19 | a0001c0001t0002g0001 a0001c0001t0005g0004 a0001c0001t0005g0020 others(16): Show |
21 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.610+3055G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134412174 | |||||||
chr9:134412280 | T | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(150): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.610+3161T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134412280 | |||||||
chr9:134412390 | C | T | 5 | a0001c0001t0003g0142 a0001c0001t0004g0148 a0001c0001t0004g0209 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.610+3271C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134412390 | |||||||
chr9:134412455 | C | T | 4 | a0001c0001t0007g0090 a0001c0001t0007g0108 a0001c0001t0032g0017 others(1): Show |
4 | HG01255.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.610+3336C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134412455 | |||||||
chr9:134412476 | A | G | 48 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(45): Show |
49 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.610+3357A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134412476 | |||||||
chr9:134412551 | G | A | 4 | a0001c0001t0007g0090 a0001c0001t0007g0108 a0001c0001t0032g0017 others(1): Show |
4 | HG01255.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.610+3432G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134412551 | |||||||
chr9:134412738 | C | T | 22 | a0001c0001t0004g0005 a0001c0001t0004g0128 a0001c0001t0004g0129 others(19): Show |
23 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.610+3619C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134412738 | |||||||
chr9:134413069 | C | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(79): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.610+3950C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134413069 | |||||||
chr9:134413391 | C | T | 8 | a0001c0001t0009g0157 a0001c0001t0010g0163 a0001c0001t0012g0038 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.611-3767C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134413391 | |||||||
chr9:134413391 | CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.611-3765_611-3754d others(14): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 134413391 | ||||||
chr9:134413756 | G | A | 183 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(180): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.611-3402G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134413756 | |||||||
chr9:134413899 | T | A | 1 | a0001c0001t0003g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.611-3259T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134413899 | |||||||
chr9:134413918 | T | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(170): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.611-3240T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134413918 | |||||||
chr9:134413932 | C | T | 5 | a0001c0001t0007g0090 a0001c0001t0007g0108 a0001c0001t0032g0017 others(2): Show |
5 | HG01255.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-3226C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134413932 | |||||||
chr9:134413975 | G | C | 1 | a0001c0001t0037g0061 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.611-3183G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134413975 | |||||||
chr9:134414036 | A | G | 1 | a0001c0001t0002g0187 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.611-3122A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414036 | |||||||
chr9:134414360 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.611-2798C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414360 | |||||||
chr9:134414374 | G | A | 18 | a0001c0001t0002g0001 a0001c0001t0005g0004 a0001c0001t0005g0020 others(15): Show |
20 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.611-2784G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414374 | |||||||
chr9:134414423 | C | G | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.611-2735C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414423 | |||||||
chr9:134414424 | G | C | 6 | a0001c0001t0007g0119 a0001c0001t0007g0203 a0001c0001t0008g0131 others(3): Show |
6 | HG02258.hp2 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.611-2734G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414424 | |||||||
chr9:134414424 | G | T | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.611-2734G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414424 | |||||||
chr9:134414425 | T | G | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.611-2733T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414425 | |||||||
chr9:134414464 | C | T | 4 | a0001c0001t0007g0090 a0001c0001t0007g0108 a0001c0001t0032g0017 others(1): Show |
4 | HG01255.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.611-2694C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414464 | |||||||
chr9:134414497 | G | A | 6 | a0001c0001t0007g0119 a0001c0001t0007g0203 a0001c0001t0008g0131 others(3): Show |
6 | HG02258.hp2 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.611-2661G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414497 | |||||||
chr9:134414727 | C | T | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.611-2431C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414727 | |||||||
chr9:134414803 | G | C | 18 | a0001c0001t0002g0001 a0001c0001t0005g0004 a0001c0001t0005g0020 others(15): Show |
20 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.611-2355G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414803 | |||||||
chr9:134414812 | G | A | 3 | a0001c0001t0008g0125 a0001c0001t0011g0121 a0001c0001t0062g0120 |
3 | HG01891.hp2 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.611-2346G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414812 | |||||||
chr9:134414845 | C | T | 5 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(2): Show |
5 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-2313C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414845 | |||||||
chr9:134414858 | G | A | 18 | a0001c0001t0002g0001 a0001c0001t0005g0004 a0001c0001t0005g0020 others(15): Show |
20 | HG00597.hp2 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.611-2300G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414858 | |||||||
chr9:134414913 | C | T | 1 | a0001c0001t0005g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.611-2245C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414913 | |||||||
chr9:134414934 | A | C | 1 | a0001c0001t0004g0205 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.611-2224A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414934 | |||||||
chr9:134414952 | A | T | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.611-2206A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134414952 | |||||||
chr9:134415089 | C | G | 8 | a0001c0001t0009g0157 a0001c0001t0010g0163 a0001c0001t0012g0038 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.611-2069C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415089 | |||||||
chr9:134415168 | G | C | 12 | a0001c0001t0004g0225 a0001c0001t0008g0141 a0001c0001t0009g0098 others(9): Show |
12 | HG02257.hp2 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.611-1990G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415168 | |||||||
chr9:134415237 | G | T | 8 | a0001c0001t0009g0157 a0001c0001t0010g0163 a0001c0001t0012g0038 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.611-1921G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415237 | |||||||
chr9:134415239 | G | C | 5 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(2): Show |
5 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-1919G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415239 | |||||||
chr9:134415260 | C | T | 91 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(88): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(90): Show |
intron_variant | MODIFIER | c.611-1898C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415260 | |||||||
chr9:134415301 | C | G | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.611-1857C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415301 | |||||||
chr9:134415301 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(138): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.611-1857C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415301 | |||||||
chr9:134415306 | G | A | 1 | a0001c0001t0003g0009 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.611-1852G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415306 | |||||||
chr9:134415387 | C | T | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.611-1771C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415387 | |||||||
chr9:134415392 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.611-1766C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415392 | |||||||
chr9:134415464 | A | AGAGGGTG others(1): Show |
40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.611-1683_611-1676d others(10): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 134415464 | ||||||
chr9:134415529 | G | C | 2 | a0001c0001t0022g0134 a0001c0001t0022g0208 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.611-1629G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415529 | |||||||
chr9:134415530 | G | A | 5 | a0001c0001t0003g0142 a0001c0001t0004g0148 a0001c0001t0004g0209 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.611-1628G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415530 | |||||||
chr9:134415669 | CAGG | C | 8 | a0001c0001t0009g0157 a0001c0001t0010g0163 a0001c0001t0012g0038 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.611-1483_611-1481d others(5): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 134415669 | ||||||
chr9:134415757 | A | G | 5 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(2): Show |
5 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-1401A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415757 | |||||||
chr9:134415972 | G | C | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.611-1186G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134415972 | |||||||
chr9:134416016 | G | GGAACAGA others(29): Show |
1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.611-1141_611-1106d others(38): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 134416016 | ||||||
chr9:134416396 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(82): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.611-762C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416396 | |||||||
chr9:134416402 | A | G | 2 | a0001c0001t0019g0059 a0001c0001t0019g0190 |
2 | HG02027.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.611-756A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416402 | |||||||
chr9:134416454 | A | G | 39 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(36): Show |
40 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.611-704A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416454 | |||||||
chr9:134416455 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.611-703C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416455 | |||||||
chr9:134416542 | C | T | 11 | a0001c0001t0004g0225 a0001c0001t0008g0141 a0001c0001t0009g0098 others(8): Show |
11 | HG02257.hp2 HG02615.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.611-616C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416542 | |||||||
chr9:134416572 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.611-586T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416572 | |||||||
chr9:134416588 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.611-570G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416588 | |||||||
chr9:134416616 | A | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(181): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.611-542A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416616 | |||||||
chr9:134416754 | C | T | 5 | a0001c0001t0009g0098 a0001c0001t0009g0130 a0001c0001t0009g0137 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-404C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416754 | |||||||
chr9:134416790 | T | A | 12 | a0001c0001t0005g0004 a0001c0001t0005g0020 a0001c0001t0005g0144 others(9): Show |
12 | HG00597.hp2 HG02040.hp2 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.611-368T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416790 | |||||||
chr9:134416856 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.611-302G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416856 | |||||||
chr9:134416857 | T | C | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.611-301T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416857 | |||||||
chr9:134416870 | C | T | 2 | a0001c0001t0014g0173 a0001c0001t0048g0024 |
2 | HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.611-288C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416870 | |||||||
chr9:134416918 | C | A | 1 | a0001c0001t0046g0152 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.611-240C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 4/9 | chr9 | 134416918 | |||||||
chr9:134417378 | C | T | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.780+51C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134417378 | |||||||
chr9:134417537 | G | C | 1 | a0001c0001t0002g0196 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.780+210G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134417537 | |||||||
chr9:134417551 | GCAGGGGC | G | 5 | a0001c0001t0009g0098 a0001c0001t0009g0130 a0001c0001t0009g0137 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.780+240_780+246del others(7): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 134417551 | ||||||
chr9:134417592 | G | A | 48 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(45): Show |
49 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.780+265G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134417592 | |||||||
chr9:134417615 | C | T | 87 | a0001c0001t0001g0194 a0001c0001t0002g0001 a0001c0001t0002g0055 others(84): Show |
90 | HG00597.hp2 HG00642.hp2 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.780+288C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134417615 | |||||||
chr9:134417634 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.780+307C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134417634 | |||||||
chr9:134417638 | G | A | 1 | a0001c0001t0008g0087 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.780+311G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134417638 | |||||||
chr9:134417647 | C | T | 1 | a0001c0001t0044g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.780+320C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134417647 | |||||||
chr9:134417799 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(93): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.780+472C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134417799 | |||||||
chr9:134417806 | C | T | 1 | a0001c0001t0049g0041 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.780+479C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134417806 | |||||||
chr9:134417807 | G | A | 1 | a0001c0001t0027g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.780+480G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134417807 | |||||||
chr9:134417841 | C | A | 2 | a0001c0001t0039g0206 a0001c0001t0061g0156 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.780+514C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134417841 | |||||||
chr9:134417926 | G | A | 2 | a0001c0001t0008g0131 a0001c0001t0041g0139 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.780+599G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134417926 | |||||||
chr9:134418040 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0064 |
2 | HG02486.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.780+713C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418040 | |||||||
chr9:134418107 | G | A | 47 | a0001c0001t0001g0194 a0001c0001t0002g0001 a0001c0001t0002g0055 others(44): Show |
49 | HG00597.hp2 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.780+780G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418107 | |||||||
chr9:134418113 | C | T | 47 | a0001c0001t0001g0194 a0001c0001t0002g0001 a0001c0001t0002g0055 others(44): Show |
49 | HG00597.hp2 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.780+786C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418113 | |||||||
chr9:134418143 | G | A | 4 | a0001c0001t0007g0090 a0001c0001t0007g0108 a0001c0001t0032g0017 others(1): Show |
4 | HG01255.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+816G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418143 | |||||||
chr9:134418149 | C | T | 1 | a0001c0001t0008g0037 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.780+822C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418149 | |||||||
chr9:134418172 | G | C | 8 | a0001c0001t0009g0157 a0001c0001t0010g0163 a0001c0001t0012g0038 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+845G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418172 | |||||||
chr9:134418228 | G | T | 40 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(37): Show |
41 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.780+901G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418228 | |||||||
chr9:134418390 | G | A | 47 | a0001c0001t0001g0194 a0001c0001t0002g0001 a0001c0001t0002g0055 others(44): Show |
49 | HG00597.hp2 HG00642.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.780+1063G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418390 | |||||||
chr9:134418543 | C | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(82): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.780+1216C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418543 | |||||||
chr9:134418607 | G | A | 8 | a0001c0001t0009g0157 a0001c0001t0010g0163 a0001c0001t0012g0038 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+1280G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418607 | |||||||
chr9:134418699 | C | G | 5 | a0001c0001t0003g0142 a0001c0001t0004g0148 a0001c0001t0004g0209 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+1372C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418699 | |||||||
chr9:134418796 | G | A | 5 | a0001c0001t0003g0142 a0001c0001t0004g0148 a0001c0001t0004g0209 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+1469G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418796 | |||||||
chr9:134418888 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.780+1561C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134418888 | |||||||
chr9:134419004 | C | T | 4 | a0001c0001t0004g0148 a0001c0001t0004g0209 a0001c0001t0023g0149 others(1): Show |
4 | HG02109.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+1677C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419004 | |||||||
chr9:134419114 | T | G | 34 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(31): Show |
35 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.780+1787T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419114 | |||||||
chr9:134419159 | C | T | 1 | a0001c0001t0005g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.780+1832C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419159 | |||||||
chr9:134419193 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.780+1866C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419193 | |||||||
chr9:134419221 | G | A | 2 | a0001c0001t0039g0206 a0001c0001t0061g0156 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.780+1894G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419221 | |||||||
chr9:134419320 | G | A | 1 | a0001c0001t0002g0110 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.780+1993G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419320 | |||||||
chr9:134419430 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.780+2103G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419430 | |||||||
chr9:134419519 | C | T | 4 | a0001c0001t0007g0090 a0001c0001t0007g0108 a0001c0001t0032g0017 others(1): Show |
4 | HG01255.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-2157C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419519 | |||||||
chr9:134419554 | G | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(116): Show |
122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.781-2122G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419554 | |||||||
chr9:134419594 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.781-2082G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419594 | |||||||
chr9:134419618 | G | A | 14 | a0001c0001t0005g0004 a0001c0001t0005g0020 a0001c0001t0005g0144 others(11): Show |
14 | HG00597.hp2 HG01891.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.781-2058G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419618 | |||||||
chr9:134419679 | A | G | 5 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(2): Show |
5 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-1997A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419679 | |||||||
chr9:134419686 | C | A | 4 | a0001c0001t0009g0157 a0001c0001t0025g0158 a0001c0001t0027g0086 others(1): Show |
4 | HG02647.hp1 HG02965.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-1990C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419686 | |||||||
chr9:134419708 | G | A | 5 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(2): Show |
5 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-1968G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419708 | |||||||
chr9:134419726 | A | G | 55 | a0001c0001t0004g0005 a0001c0001t0004g0128 a0001c0001t0004g0129 others(52): Show |
56 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(53): Show |
intron_variant | MODIFIER | c.781-1950A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419726 | |||||||
chr9:134419874 | C | T | 2 | a0001c0001t0039g0206 a0001c0001t0061g0156 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.781-1802C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419874 | |||||||
chr9:134419959 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.781-1717C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134419959 | |||||||
chr9:134420084 | C | T | 7 | a0001c0001t0012g0038 a0001c0001t0012g0151 a0001c0001t0012g0159 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-1592C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134420084 | |||||||
chr9:134420149 | G | A | 3 | a0001c0001t0039g0206 a0001c0001t0061g0156 a0001c0001t0062g0120 |
3 | HG02717.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.781-1527G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134420149 | |||||||
chr9:134420170 | C | T | 2 | a0001c0001t0003g0080 a0001c0001t0003g0166 |
2 | HG00735.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.781-1506C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134420170 | |||||||
chr9:134420428 | A | G | 7 | a0001c0001t0001g0218 a0001c0001t0002g0029 a0001c0001t0002g0219 others(4): Show |
7 | HG00738.hp2 HG01106.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-1248A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134420428 | |||||||
chr9:134420514 | G | A | 1 | a0001c0001t0060g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.781-1162G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134420514 | |||||||
chr9:134420514 | G | C | 3 | a0001c0001t0002g0055 a0001c0001t0002g0081 a0001c0001t0057g0053 |
3 | HG01099.hp2 HG01256.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.781-1162G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134420514 | |||||||
chr9:134420523 | T | C | 18 | a0001c0001t0007g0119 a0001c0001t0007g0203 a0001c0001t0008g0087 others(15): Show |
18 | HG02257.hp2 HG02258.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.781-1153T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134420523 | |||||||
chr9:134420547 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.781-1129C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134420547 | |||||||
chr9:134420814 | C | G | 1 | a0001c0001t0059g0210 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.781-862C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134420814 | |||||||
chr9:134420876 | C | T | 1 | a0001c0001t0005g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.781-800C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134420876 | |||||||
chr9:134420982 | T | C | 37 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0069 others(34): Show |
37 | HG00597.hp2 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.781-694T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134420982 | |||||||
chr9:134421101 | C | G | 29 | a0001c0001t0004g0005 a0001c0001t0004g0128 a0001c0001t0004g0129 others(26): Show |
30 | HG01884.hp2 HG01891.hp2 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.781-575C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134421101 | |||||||
chr9:134421128 | C | T | 15 | a0001c0001t0007g0119 a0001c0001t0007g0203 a0001c0001t0008g0087 others(12): Show |
15 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.781-548C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134421128 | |||||||
chr9:134421241 | G | A | 7 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0081 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.781-435G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134421241 | |||||||
chr9:134421323 | A | G | 5 | a0001c0001t0003g0060 a0001c0001t0019g0059 a0001c0001t0019g0190 others(2): Show |
5 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-353A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134421323 | |||||||
chr9:134421561 | G | T | 15 | a0001c0001t0005g0004 a0001c0001t0005g0020 a0001c0001t0005g0144 others(12): Show |
15 | HG00597.hp2 HG01891.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.781-115G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134421561 | |||||||
chr9:134421563 | C | T | 2 | a0001c0001t0019g0059 a0001c0001t0019g0190 |
2 | HG02027.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.781-113C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 5/9 | chr9 | 134421563 | |||||||
chr9:134421814 | C | T | 1 | a0001c0001t0034g0011 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.910+9C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134421814 | |||||||
chr9:134421873 | C | A | 52 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(49): Show |
53 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.910+68C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134421873 | |||||||
chr9:134421873 | CCTCCCGG others(11): Show |
C | 1 | a0001c0001t0052g0012 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.910+78_910+95delTA others(16): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 134421873 | ||||||
chr9:134421879 | G | A | 6 | a0001c0001t0012g0038 a0001c0001t0012g0151 a0001c0001t0012g0159 others(3): Show |
6 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.910+74G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134421879 | |||||||
chr9:134421990 | C | T | 2 | a0001c0001t0014g0085 a0001c0001t0014g0173 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.910+185C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134421990 | |||||||
chr9:134422023 | C | G | 5 | a0001c0001t0006g0021 a0001c0001t0014g0180 a0001c0001t0039g0206 others(2): Show |
5 | HG01099.hp1 HG02145.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.910+218C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422023 | |||||||
chr9:134422040 | ATCTCCCA others(11): Show |
A | 7 | a0001c0001t0003g0060 a0001c0001t0014g0085 a0001c0001t0014g0173 others(4): Show |
7 | HG01074.hp1 HG01257.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.910+265_910+282del others(18): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 134422040 | ||||||
chr9:134422133 | A | ACTCCTGG others(13): Show |
4 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0022g0134 others(1): Show |
4 | HG00099.hp1 HG00099.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.910+373_910+392dup others(20): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 134422133 | ||||||
chr9:134422152 | C | T | 3 | a0001c0001t0027g0086 a0001c0001t0045g0161 a0001c0001t0060g0100 |
3 | HG02647.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.910+347C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422152 | |||||||
chr9:134422283 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0103 a0001c0001t0001g0107 |
3 | HG00741.hp1 HG01074.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.910+478C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422283 | |||||||
chr9:134422339 | A | AC | 5 | a0001c0001t0002g0110 a0001c0001t0008g0141 a0001c0001t0012g0151 others(2): Show |
5 | HG02055.hp2 HG03516.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.910+539dupC | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 134422339 | ||||||
chr9:134422362 | C | T | 18 | a0001c0001t0003g0044 a0001c0001t0003g0069 a0001c0001t0003g0142 others(15): Show |
18 | HG01069.hp2 HG01099.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.910+557C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422362 | |||||||
chr9:134422364 | C | T | 2 | a0001c0001t0003g0080 a0001c0001t0003g0166 |
2 | HG00735.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.910+559C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422364 | |||||||
chr9:134422368 | C | T | 1 | a0001c0001t0005g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.910+563C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422368 | |||||||
chr9:134422387 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.910+582G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422387 | |||||||
chr9:134422409 | C | A | 3 | a0001c0001t0004g0133 a0001c0001t0004g0202 a0001c0001t0004g0225 |
3 | HG00735.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.910+604C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422409 | |||||||
chr9:134422479 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.910+674G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422479 | |||||||
chr9:134422532 | C | T | 1 | a0001c0001t0003g0221 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.910+727C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422532 | |||||||
chr9:134422546 | C | T | 1 | a0001c0001t0013g0188 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.910+741C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422546 | |||||||
chr9:134422550 | T | C | 1 | a0001c0001t0060g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.910+745T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422550 | |||||||
chr9:134422557 | GTCCCCAC others(47): Show |
G | 53 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(50): Show |
54 | HG00735.hp1 HG01109.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.910+782_910+835del others(54): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 134422557 | ||||||
chr9:134422587 | GGGACACT others(47): Show |
G | 9 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0069 others(6): Show |
9 | HG01069.hp2 HG02145.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.910+794_910+847del others(54): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 134422587 | ||||||
chr9:134422642 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0033g0171 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.910+837G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422642 | |||||||
chr9:134422659 | C | T | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | NA18939.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.910+854C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422659 | |||||||
chr9:134422688 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.910+883C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134422688 | |||||||
chr9:134423049 | G | A | 1 | a0001c0001t0060g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.910+1244G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423049 | |||||||
chr9:134423097 | C | T | 12 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0081 others(9): Show |
14 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.910+1292C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423097 | |||||||
chr9:134423114 | A | C | 2 | a0001c0001t0001g0194 a0001c0001t0036g0201 |
2 | HG00642.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.910+1309A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423114 | |||||||
chr9:134423145 | C | G | 7 | a0001c0001t0005g0004 a0001c0001t0005g0144 a0001c0001t0005g0183 others(4): Show |
7 | HG00597.hp2 HG02040.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.910+1340C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423145 | |||||||
chr9:134423169 | G | C | 2 | a0001c0001t0027g0086 a0001c0001t0045g0161 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.910+1364G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423169 | |||||||
chr9:134423319 | C | T | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.910+1514C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423319 | |||||||
chr9:134423367 | C | G | 4 | a0001c0001t0012g0038 a0001c0001t0012g0151 a0001c0001t0012g0159 others(1): Show |
4 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.910+1562C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423367 | |||||||
chr9:134423447 | G | A | 16 | a0001c0001t0007g0119 a0001c0001t0007g0203 a0001c0001t0008g0087 others(13): Show |
16 | HG02257.hp2 HG02258.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.910+1642G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423447 | |||||||
chr9:134423645 | G | A | 3 | a0001c0001t0027g0086 a0001c0001t0045g0161 a0001c0001t0060g0100 |
3 | HG02647.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.910+1840G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423645 | |||||||
chr9:134423653 | C | T | 2 | a0001c0001t0027g0086 a0001c0001t0045g0161 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.910+1848C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423653 | |||||||
chr9:134423718 | A | G | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.910+1913A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423718 | |||||||
chr9:134423760 | G | A | 1 | a0001c0001t0048g0024 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.910+1955G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423760 | |||||||
chr9:134423917 | C | T | 1 | a0001c0001t0048g0024 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.910+2112C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134423917 | |||||||
chr9:134423973 | AGGTCCGA others(5): Show |
A | 3 | a0001c0001t0004g0133 a0001c0001t0004g0202 a0001c0001t0004g0225 |
3 | HG00735.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.910+2170_910+2181d others(14): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 134423973 | ||||||
chr9:134424090 | G | A | 2 | a0001c0001t0005g0183 a0001c0001t0005g0184 |
2 | HG00597.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.910+2285G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134424090 | |||||||
chr9:134424342 | C | A | 7 | a0001c0001t0002g0055 a0001c0001t0002g0081 a0001c0001t0002g0214 others(4): Show |
7 | HG01099.hp2 HG01169.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.910+2537C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134424342 | |||||||
chr9:134424374 | G | A | 6 | a0001c0001t0012g0038 a0001c0001t0012g0151 a0001c0001t0012g0159 others(3): Show |
6 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.910+2569G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134424374 | |||||||
chr9:134424413 | G | C | 91 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0069 others(88): Show |
92 | HG00597.hp2 HG00735.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.910+2608G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134424413 | |||||||
chr9:134424546 | A | G | 35 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0069 others(32): Show |
35 | HG00597.hp2 HG00735.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.910+2741A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134424546 | |||||||
chr9:134424686 | A | G | 1 | a0001c0001t0027g0086 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.910+2881A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134424686 | |||||||
chr9:134424695 | T | G | 1 | a0001c0001t0001g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.910+2890T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134424695 | |||||||
chr9:134425158 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.910+3353G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425158 | |||||||
chr9:134425180 | G | A | 1 | a0001c0001t0009g0157 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.910+3375G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425180 | |||||||
chr9:134425394 | G | A | 1 | a0001c0001t0059g0210 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.910+3589G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425394 | |||||||
chr9:134425487 | C | T | 35 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0069 others(32): Show |
35 | HG00597.hp2 HG00735.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.911-3621C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425487 | |||||||
chr9:134425534 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.911-3574G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425534 | |||||||
chr9:134425546 | T | TGGGGGGT others(12): Show |
1 | a0001c0001t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.911-3548_911-3530d others(21): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 134425546 | ||||||
chr9:134425553 | T | G | 1 | a0001c0001t0002g0110 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.911-3555T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425553 | |||||||
chr9:134425553 | T | TG | 25 | a0001c0001t0001g0050 a0001c0001t0001g0093 a0001c0001t0001g0095 others(22): Show |
25 | HG00408.hp1 HG00597.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.911-3546dupG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 134425553 | ||||||
chr9:134425555 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.911-3553G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425555 | |||||||
chr9:134425560 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.911-3548G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425560 | |||||||
chr9:134425560 | G | T | 31 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0004g0005 others(28): Show |
32 | HG00735.hp1 HG01243.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.911-3548G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425560 | |||||||
chr9:134425565 | A | G | 1 | a0001c0004t0005g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.911-3543A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425565 | |||||||
chr9:134425644 | G | A | 1 | a0001c0001t0008g0125 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.911-3464G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425644 | |||||||
chr9:134425804 | C | T | 2 | a0001c0001t0027g0086 a0001c0001t0045g0161 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.911-3304C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425804 | |||||||
chr9:134425955 | C | T | 4 | a0001c0001t0006g0021 a0001c0001t0014g0180 a0001c0001t0039g0206 others(1): Show |
4 | HG01099.hp1 HG02145.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.911-3153C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134425955 | |||||||
chr9:134426004 | G | A | 1 | a0001c0001t0056g0143 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.911-3104G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134426004 | |||||||
chr9:134426010 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0033g0171 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.911-3098G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134426010 | |||||||
chr9:134426017 | AG | A | 4 | a0001c0001t0006g0021 a0001c0001t0014g0180 a0001c0001t0039g0206 others(1): Show |
4 | HG01099.hp1 HG02145.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.911-3087delG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 134426017 | ||||||
chr9:134426232 | G | A | 1 | a0001c0001t0057g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.911-2876G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134426232 | |||||||
chr9:134426332 | C | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(68): Show |
73 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(70): Show |
intron_variant | MODIFIER | c.911-2776C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134426332 | |||||||
chr9:134426371 | T | A | 3 | a0001c0001t0022g0134 a0001c0001t0022g0208 a0001c0004t0005g0126 |
3 | HG02976.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.911-2737T>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134426371 | |||||||
chr9:134426507 | T | C | 2 | a0001c0001t0014g0085 a0001c0001t0014g0173 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.911-2601T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134426507 | |||||||
chr9:134426509 | C | T | 2 | a0001c0001t0009g0157 a0001c0001t0025g0158 |
2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.911-2599C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134426509 | |||||||
chr9:134426536 | C | T | 14 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0002g0081 others(11): Show |
16 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.911-2572C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134426536 | |||||||
chr9:134426654 | C | T | 1 | a0001c0001t0017g0057 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.911-2454C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134426654 | |||||||
chr9:134426995 | G | A | 15 | a0001c0001t0007g0119 a0001c0001t0007g0203 a0001c0001t0008g0087 others(12): Show |
15 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.911-2113G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134426995 | |||||||
chr9:134427159 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.911-1949T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134427159 | |||||||
chr9:134427174 | A | C | 1 | a0001c0001t0049g0041 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.911-1934A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134427174 | |||||||
chr9:134427285 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.911-1823G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134427285 | |||||||
chr9:134427306 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.911-1802G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134427306 | |||||||
chr9:134427419 | G | A | 1 | a0001c0004t0005g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.911-1689G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134427419 | |||||||
chr9:134427670 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.911-1438G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134427670 | |||||||
chr9:134428168 | C | A | 10 | a0001c0001t0009g0098 a0001c0001t0009g0130 a0001c0001t0009g0137 others(7): Show |
10 | HG02257.hp2 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.911-940C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134428168 | |||||||
chr9:134428347 | G | A | 1 | a0001c0001t0059g0210 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.911-761G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134428347 | |||||||
chr9:134428388 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.911-720G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134428388 | |||||||
chr9:134428394 | AGGCTGCT others(94): Show |
A | 9 | a0001c0001t0009g0098 a0001c0001t0009g0130 a0001c0001t0009g0137 others(6): Show |
9 | HG02257.hp2 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.911-641_911-541del | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 134428394 | ||||||
chr9:134428411 | C | G | 2 | a0001c0001t0027g0086 a0001c0001t0045g0161 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.911-697C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134428411 | |||||||
chr9:134428471 | C | T | 1 | a0001c0001t0048g0024 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.911-637C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134428471 | |||||||
chr9:134428566 | C | CCA | 4 | a0001c0001t0006g0021 a0001c0001t0014g0180 a0001c0001t0039g0206 others(1): Show |
4 | HG01099.hp1 HG02145.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.911-541_911-540ins others(2): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 134428566 | ||||||
chr9:134428568 | G | C | 4 | a0001c0001t0006g0021 a0001c0001t0014g0180 a0001c0001t0039g0206 others(1): Show |
4 | HG01099.hp1 HG02145.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.911-540G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134428568 | |||||||
chr9:134428635 | G | A | 7 | a0001c0001t0006g0021 a0001c0001t0014g0180 a0001c0001t0022g0134 others(4): Show |
7 | HG01099.hp1 HG02145.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.911-473G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134428635 | |||||||
chr9:134428791 | C | T | 1 | a0001c0001t0007g0035 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.911-317C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134428791 | |||||||
chr9:134428972 | C | T | 4 | a0001c0001t0007g0090 a0001c0001t0007g0108 a0001c0001t0032g0017 others(1): Show |
4 | HG01255.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.911-136C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134428972 | |||||||
chr9:134429009 | G | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(179): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.911-99G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 6/9 | chr9 | 134429009 | |||||||
chr9:134429310 | A | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(172): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1043+70A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134429310 | |||||||
chr9:134429410 | T | G | 9 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0069 others(6): Show |
9 | HG01069.hp2 HG02145.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.1043+170T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134429410 | |||||||
chr9:134429619 | G | A | 1 | a0001c0001t0007g0203 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1043+379G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134429619 | |||||||
chr9:134429649 | G | A | 2 | a0001c0001t0019g0059 a0001c0001t0019g0190 |
2 | HG02027.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1043+409G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134429649 | |||||||
chr9:134429682 | G | A | 2 | a0001c0001t0007g0119 a0001c0001t0007g0203 |
2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1043+442G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134429682 | |||||||
chr9:134429754 | C | A | 6 | a0001c0001t0007g0119 a0001c0001t0007g0203 a0001c0001t0008g0087 others(3): Show |
6 | HG02258.hp2 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1043+514C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134429754 | |||||||
chr9:134429835 | A | G | 1 | a0001c0001t0060g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1043+595A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134429835 | |||||||
chr9:134429851 | C | T | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1043+611C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134429851 | |||||||
chr9:134429902 | T | C | 1 | a0001c0001t0046g0152 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1043+662T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134429902 | |||||||
chr9:134429914 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0033g0171 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1043+674C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134429914 | |||||||
chr9:134429948 | C | T | 1 | a0001c0001t0050g0042 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1043+708C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134429948 | |||||||
chr9:134429971 | C | T | 2 | a0001c0001t0027g0086 a0001c0001t0045g0161 |
2 | HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1043+731C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134429971 | |||||||
chr9:134430046 | C | T | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1043+806C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430046 | |||||||
chr9:134430060 | G | A | 1 | a0001c0001t0046g0152 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1043+820G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430060 | |||||||
chr9:134430069 | G | A | 2 | a0001c0001t0001g0164 a0001c0001t0033g0171 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1043+829G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430069 | |||||||
chr9:134430113 | C | G | 1 | a0001c0001t0033g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1043+873C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430113 | |||||||
chr9:134430133 | A | G | 111 | a0001c0001t0001g0164 a0001c0001t0002g0001 a0001c0001t0002g0055 others(108): Show |
114 | HG00597.hp2 HG00735.hp1 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.1043+893A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430133 | |||||||
chr9:134430133 | A | T | 1 | a0001c0001t0003g0069 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1043+893A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430133 | |||||||
chr9:134430138 | G | A | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1043+898G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430138 | |||||||
chr9:134430177 | C | T | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1043+937C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430177 | |||||||
chr9:134430207 | C | T | 1 | a0001c0001t0005g0200 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1043+967C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430207 | |||||||
chr9:134430252 | G | A | 10 | a0001c0001t0009g0098 a0001c0001t0009g0130 a0001c0001t0009g0137 others(7): Show |
10 | HG02257.hp2 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1043+1012G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430252 | |||||||
chr9:134430420 | G | A | 3 | a0001c0001t0022g0134 a0001c0001t0022g0208 a0001c0004t0005g0126 |
3 | HG02976.hp2 HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1043+1180G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430420 | |||||||
chr9:134430462 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1043+1222G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430462 | |||||||
chr9:134430508 | C | A | 1 | a0001c0001t0001g0019 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1043+1268C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430508 | |||||||
chr9:134430564 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1043+1324G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430564 | |||||||
chr9:134430641 | TC | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(96): Show |
104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.1044-1260delC | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 134430641 | ||||||
chr9:134430652 | G | C | 2 | a0001c0001t0014g0085 a0001c0001t0014g0173 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1044-1253G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430652 | |||||||
chr9:134430788 | C | T | 4 | a0001c0001t0007g0090 a0001c0001t0011g0121 a0001c0001t0011g0140 others(1): Show |
4 | HG01255.hp1 HG01891.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044-1117C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430788 | |||||||
chr9:134430841 | A | C | 1 | a0001c0001t0046g0152 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1044-1064A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430841 | |||||||
chr9:134430855 | T | C | 1 | a0001c0001t0003g0073 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1044-1050T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430855 | |||||||
chr9:134430864 | T | G | 13 | a0001c0001t0001g0169 a0001c0001t0002g0048 a0001c0001t0002g0054 others(10): Show |
13 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1044-1041T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134430864 | |||||||
chr9:134431061 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1044-844T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134431061 | |||||||
chr9:134431093 | G | C | 16 | a0001c0001t0003g0025 a0001c0001t0003g0043 a0001c0001t0003g0044 others(13): Show |
16 | HG01069.hp2 HG02145.hp1 HG02293.hp1 others(13): Show |
intron_variant | MODIFIER | c.1044-812G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134431093 | |||||||
chr9:134431178 | G | A | 1 | a0001c0001t0003g0221 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1044-727G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134431178 | |||||||
chr9:134431228 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1044-677G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134431228 | |||||||
chr9:134431356 | G | T | 12 | a0001c0001t0003g0025 a0001c0001t0003g0043 a0001c0001t0003g0044 others(9): Show |
12 | HG01069.hp2 HG01433.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1044-549G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134431356 | |||||||
chr9:134431460 | C | T | 1 | a0001c0001t0005g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1044-445C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134431460 | |||||||
chr9:134431650 | G | A | 4 | a0001c0001t0019g0059 a0001c0001t0019g0190 a0001c0001t0054g0018 others(1): Show |
4 | HG01074.hp1 HG01257.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044-255G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134431650 | |||||||
chr9:134431662 | T | C | 1 | a0001c0001t0004g0128 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1044-243T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134431662 | |||||||
chr9:134431695 | AGGGCCAG others(130): Show |
A | 4 | a0001c0001t0008g0125 a0001c0001t0025g0158 a0001c0001t0026g0127 others(1): Show |
4 | HG02717.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1044-207_1044-71de others(1): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 134431695 | ||||||
chr9:134431811 | G | A | 4 | a0001c0001t0019g0059 a0001c0001t0019g0190 a0001c0001t0054g0018 others(1): Show |
4 | HG01074.hp1 HG01257.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044-94G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134431811 | |||||||
chr9:134431877 | A | T | 1 | a0001c0001t0006g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1044-28A>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 7/9 | chr9 | 134431877 | |||||||
chr9:134432030 | G | A | 2 | a0001c0001t0014g0085 a0001c0001t0014g0173 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1135+34G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432030 | |||||||
chr9:134432064 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0216 |
2 | HG00408.hp2 HG00423.hp1 |
intron_variant | MODIFIER | c.1135+68C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432064 | |||||||
chr9:134432102 | A | G | 19 | a0001c0001t0005g0004 a0001c0001t0005g0020 a0001c0001t0005g0144 others(16): Show |
19 | HG00597.hp2 HG01891.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.1135+106A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432102 | |||||||
chr9:134432131 | C | A | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1135+135C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432131 | |||||||
chr9:134432179 | G | T | 1 | a0001c0001t0053g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1135+183G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432179 | |||||||
chr9:134432215 | G | GA | 4 | a0001c0001t0002g0223 a0001c0001t0003g0221 a0001c0001t0003g0222 others(1): Show |
4 | HG00738.hp2 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.1135+220dupA | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 134432215 | ||||||
chr9:134432236 | T | C | 14 | a0001c0001t0001g0164 a0001c0001t0009g0098 a0001c0001t0009g0130 others(11): Show |
14 | HG02257.hp2 HG02615.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.1135+240T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432236 | |||||||
chr9:134432274 | T | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1135+278T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432274 | |||||||
chr9:134432584 | C | G | 1 | a0001c0001t0047g0116 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1135+588C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432584 | |||||||
chr9:134432597 | C | G | 1 | a0001c0001t0048g0024 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1135+601C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432597 | |||||||
chr9:134432626 | T | C | 38 | a0001c0001t0005g0004 a0001c0001t0005g0020 a0001c0001t0005g0144 others(35): Show |
38 | HG00597.hp2 HG01074.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.1135+630T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432626 | |||||||
chr9:134432720 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0033g0171 |
2 | HG03139.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1135+724C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432720 | |||||||
chr9:134432753 | C | A | 1 | a0001c0001t0019g0059 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1135+757C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432753 | |||||||
chr9:134432806 | A | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(172): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1135+810A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134432806 | |||||||
chr9:134433062 | G | A | 19 | a0001c0001t0005g0004 a0001c0001t0005g0020 a0001c0001t0005g0144 others(16): Show |
19 | HG00597.hp2 HG01891.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.1136-1040G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134433062 | |||||||
chr9:134433252 | G | A | 1 | a0001c0001t0003g0166 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1136-850G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134433252 | |||||||
chr9:134433422 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0220 |
2 | HG01070.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1136-680G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134433422 | |||||||
chr9:134433462 | G | T | 2 | a0001c0001t0014g0180 a0001c0001t0046g0152 |
2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1136-640G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134433462 | |||||||
chr9:134433484 | A | AGGCCAAG others(32): Show |
9 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0007g0119 others(6): Show |
9 | HG00735.hp1 HG01243.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1136-579_1136-541d others(41): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 134433484 | ||||||
chr9:134433484 | AGGCCAAG others(32): Show |
A | 2 | a0001c0001t0039g0206 a0001c0001t0061g0156 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1136-579_1136-541d others(41): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 134433484 | ||||||
chr9:134433550 | C | T | 2 | a0001c0001t0022g0134 a0001c0001t0022g0208 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1136-552C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134433550 | |||||||
chr9:134433593 | G | C | 1 | a0001c0001t0008g0131 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1136-509G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134433593 | |||||||
chr9:134433616 | G | A | 1 | a0001c0001t0008g0037 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1136-486G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134433616 | |||||||
chr9:134433813 | G | A | 5 | a0001c0001t0002g0055 a0001c0001t0002g0081 a0001c0001t0057g0053 others(2): Show |
5 | HG01099.hp2 HG01169.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1136-289G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134433813 | |||||||
chr9:134433923 | G | A | 1 | a0001c0001t0045g0161 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1136-179G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134433923 | |||||||
chr9:134433952 | G | A | 2 | a0001c0001t0014g0180 a0001c0001t0046g0152 |
2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1136-150G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134433952 | |||||||
chr9:134433970 | C | T | 1 | a0001c0001t0003g0044 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1136-132C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134433970 | |||||||
chr9:134433976 | T | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1136-126T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134433976 | |||||||
chr9:134434012 | T | C | 14 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0007g0119 others(11): Show |
14 | HG00735.hp1 HG01243.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1136-90T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134434012 | |||||||
chr9:134434026 | C | T | 3 | a0001c0001t0023g0149 a0001c0001t0023g0150 a0001c0001t0045g0161 |
3 | HG02647.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1136-76C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134434026 | |||||||
chr9:134434053 | C | T | 9 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0007g0119 others(6): Show |
9 | HG00735.hp1 HG01243.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1136-49C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 8/9 | chr9 | 134434053 | |||||||
chr9:134434256 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1241+49C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434256 | |||||||
chr9:134434271 | C | A | 1 | a0001c0001t0047g0116 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1241+64C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434271 | |||||||
chr9:134434368 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1241+161C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434368 | |||||||
chr9:134434495 | C | G | 4 | a0001c0001t0002g0223 a0001c0001t0003g0221 a0001c0001t0003g0222 others(1): Show |
4 | HG00738.hp2 HG01106.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241+288C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434495 | |||||||
chr9:134434536 | C | T | 4 | a0001c0001t0019g0059 a0001c0001t0019g0190 a0001c0001t0054g0018 others(1): Show |
4 | HG01074.hp1 HG01257.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241+329C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434536 | |||||||
chr9:134434562 | A | G | 80 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(77): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.1241+355A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434562 | |||||||
chr9:134434655 | C | T | 4 | a0001c0001t0012g0038 a0001c0001t0012g0151 a0001c0001t0012g0159 others(1): Show |
4 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241+448C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434655 | |||||||
chr9:134434676 | C | T | 2 | a0001c0001t0056g0143 a0001c0004t0005g0126 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1241+469C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434676 | |||||||
chr9:134434763 | T | C | 12 | a0001c0001t0009g0098 a0001c0001t0009g0130 a0001c0001t0009g0137 others(9): Show |
12 | HG02257.hp2 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1241+556T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434763 | |||||||
chr9:134434794 | C | T | 12 | a0001c0001t0009g0098 a0001c0001t0009g0130 a0001c0001t0009g0137 others(9): Show |
12 | HG02257.hp2 HG02615.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.1241+587C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434794 | |||||||
chr9:134434861 | C | CG | 24 | a0001c0001t0003g0166 a0001c0001t0005g0004 a0001c0001t0005g0020 others(21): Show |
24 | HG00597.hp2 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1241+658dupG | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 134434861 | ||||||
chr9:134434861 | C | CGG | 12 | a0001c0001t0003g0080 a0001c0001t0009g0098 a0001c0001t0009g0138 others(9): Show |
12 | HG00735.hp1 HG01074.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1241+657_1241+658d others(4): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 134434861 | ||||||
chr9:134434861 | C | CGGG | 6 | a0001c0001t0008g0037 a0001c0001t0016g0155 a0001c0001t0016g0207 others(3): Show |
6 | HG02257.hp2 HG02451.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241+656_1241+658d others(5): Show |
RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 134434861 | ||||||
chr9:134434866 | A | C | 1 | a0001c0001t0012g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1241+659A>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434866 | |||||||
chr9:134434866 | A | G | 55 | a0001c0001t0003g0080 a0001c0001t0003g0166 a0001c0001t0005g0004 others(52): Show |
55 | HG00597.hp2 HG00735.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.1241+659A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434866 | |||||||
chr9:134434867 | G | T | 1 | a0001c0001t0003g0044 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1241+660G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434867 | |||||||
chr9:134434872 | T | G | 2 | a0001c0001t0039g0206 a0001c0001t0061g0156 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1241+665T>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434872 | |||||||
chr9:134434953 | C | T | 2 | a0001c0001t0023g0149 a0001c0001t0023g0150 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1241+746C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434953 | |||||||
chr9:134434955 | C | T | 1 | a0001c0001t0004g0005 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1241+748C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134434955 | |||||||
chr9:134435247 | G | C | 3 | a0001c0001t0001g0013 a0001c0001t0018g0104 a0001c0001t0018g0105 |
3 | HG00423.hp2 NA18944.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1241+1040G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435247 | |||||||
chr9:134435271 | C | G | 2 | a0001c0001t0039g0206 a0001c0001t0061g0156 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1241+1064C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435271 | |||||||
chr9:134435293 | G | C | 1 | a0001c0005t0001g0193 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1241+1086G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435293 | |||||||
chr9:134435361 | C | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.1242-1106C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435361 | |||||||
chr9:134435402 | C | G | 35 | a0001c0001t0005g0004 a0001c0001t0005g0020 a0001c0001t0005g0144 others(32): Show |
35 | HG00597.hp2 HG01109.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.1242-1065C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435402 | |||||||
chr9:134435593 | G | A | 1 | a0001c0001t0002g0001 | 3 | HG01069.hp1 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1242-874G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435593 | |||||||
chr9:134435626 | G | A | 2 | a0001c0001t0054g0018 a0001c0001t0055g0167 |
2 | HG01074.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.1242-841G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435626 | |||||||
chr9:134435635 | C | T | 1 | a0001c0001t0002g0212 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1242-832C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435635 | |||||||
chr9:134435666 | G | C | 5 | a0001c0001t0009g0098 a0001c0001t0009g0130 a0001c0001t0009g0137 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1242-801G>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435666 | |||||||
chr9:134435770 | G | T | 16 | a0001c0001t0005g0004 a0001c0001t0005g0020 a0001c0001t0005g0144 others(13): Show |
16 | HG00597.hp2 HG01891.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1242-697G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435770 | |||||||
chr9:134435781 | T | C | 4 | a0001c0001t0012g0038 a0001c0001t0012g0151 a0001c0001t0012g0159 others(1): Show |
4 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1242-686T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435781 | |||||||
chr9:134435791 | G | T | 6 | a0001c0001t0010g0101 a0001c0001t0010g0122 a0001c0001t0010g0163 others(3): Show |
6 | HG01943.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1242-676G>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435791 | |||||||
chr9:134435842 | C | T | 2 | a0001c0001t0019g0059 a0001c0001t0019g0190 |
2 | HG02027.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1242-625C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435842 | |||||||
chr9:134435853 | G | A | 1 | a0001c0001t0051g0023 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1242-614G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435853 | |||||||
chr9:134435928 | C | T | 1 | a0001c0001t0059g0210 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1242-539C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435928 | |||||||
chr9:134435953 | C | A | 1 | a0001c0001t0008g0037 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1242-514C>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134435953 | |||||||
chr9:134436009 | T | C | 4 | a0001c0001t0001g0030 a0001c0001t0001g0051 a0001c0001t0001g0056 others(1): Show |
4 | HG00733.hp1 HG01346.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1242-458T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134436009 | |||||||
chr9:134436058 | C | T | 1 | a0001c0004t0005g0126 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1242-409C>T | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134436058 | |||||||
chr9:134436228 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1242-239G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134436228 | |||||||
chr9:134436231 | C | G | 1 | a0001c0001t0060g0100 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1242-236C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134436231 | |||||||
chr9:134436307 | C | G | 1 | a0001c0001t0012g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1242-160C>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134436307 | |||||||
chr9:134436329 | T | C | 38 | a0001c0001t0005g0004 a0001c0001t0005g0020 a0001c0001t0005g0144 others(35): Show |
38 | HG00597.hp2 HG01074.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.1242-138T>C | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134436329 | |||||||
chr9:134436370 | G | A | 19 | a0001c0001t0005g0004 a0001c0001t0005g0020 a0001c0001t0005g0144 others(16): Show |
19 | HG00597.hp2 HG01891.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.1242-97G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134436370 | |||||||
chr9:134436398 | A | G | 2 | a0001c0001t0039g0206 a0001c0001t0061g0156 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1242-69A>G | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134436398 | |||||||
chr9:134436440 | G | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(77): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.1242-27G>A | RXRA | ENSG00000186350.12 | transcript | ENST00000481739.2 | protein_coding | 9/9 | chr9 | 134436440 |