Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 949 |
| ensemblid | ENSG00000073060.17 |
| hgncid | 1664 |
| symbol | SCARB1 |
| name | scavenger receptor class B member 1 |
| refseq_nuc | NM_005505.5 |
| refseq_prot | NP_005496.4 |
| ensembl_nuc | ENST00000261693.11 |
| ensembl_prot | ENSP00000261693.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 124776856 |
| end | 124863864 |
| strand | - |
| ver | v1.2 |
| region | chr12:124776856-124863864 |
| region5000 | chr12:124771856-124868864 |
| regionname0 | SCARB1_chr12_124776856_124863864 |
| regionname5000 | SCARB1_chr12_124771856_124868864 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 509 | 330 | 84 | 55 | 140 | 6 | 43 | 99 | SCARB1_chr12_124771856_124868864 | SCARB1 | MGCSA others(504): Show |
chr12 | 124771856 | 124868864 |
| a0002 | 0/0 | 509 | 17 | 3 | 9 | 0 | 4 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | MSCSA others(504): Show |
chr12 | 124771856 | 124868864 |
| a0003 | 0/0 | 509 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | MGCSA others(504): Show |
chr12 | 124771856 | 124868864 |
| a0004 | 0/0 | 509 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | MGCSA others(504): Show |
chr12 | 124771856 | 124868864 |
| a0005 | 0/0 | 509 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | MGCSA others(504): Show |
chr12 | 124771856 | 124868864 |
| a0006 | 0/0 | 509 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | MGCSA others(504): Show |
chr12 | 124771856 | 124868864 |
| a0007 | 0/0 | 509 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | MGCSA others(504): Show |
chr12 | 124771856 | 124868864 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1527 | 153 | 59 | 33 | 44 | 4 | 12 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0001c0002 | 1/0 | 1527 | 76 | 4 | 17 | 30 | 2 | 22 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0001c0003 | 0/0 | 1527 | 57 | 0 | 5 | 51 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0001c0004 | 0/0 | 1527 | 17 | 4 | 0 | 9 | 0 | 4 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0001c0005 | 0/0 | 1527 | 12 | 12 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0001c0007 | 0/0 | 1527 | 8 | 0 | 0 | 6 | 0 | 2 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0001c0010 | 0/0 | 1527 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0001c0013 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0001c0016 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0001c0017 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0001c0018 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0001c0020 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0002c0006 | 0/0 | 1527 | 11 | 3 | 6 | 0 | 2 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGAG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0002c0008 | 0/0 | 1527 | 6 | 0 | 3 | 0 | 2 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGAG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0003c0009 | 0/0 | 1527 | 2 | 1 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0003c0019 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0004c0011 | 0/0 | 1527 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0005c0012 | 0/0 | 1527 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0006c0015 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 | ||
| a0007c0014 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | ATGGG others(1522): Show |
chr12 | 124771856 | 124868864 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3407 | 57 | 7 | 21 | 16 | 2 | 11 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0002 | 0/0 | 3407 | 17 | 0 | 1 | 16 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0003 | 0/1 | 3405 | 33 | 17 | 3 | 9 | 2 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0004 | 0/0 | 3405 | 9 | 7 | 1 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0005 | 0/0 | 3405 | 6 | 3 | 3 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0006 | 0/0 | 3405 | 8 | 7 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0007 | 0/0 | 3407 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0008 | 0/0 | 3407 | 9 | 9 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0011 | 0/0 | 3407 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0012 | 0/0 | 3405 | 3 | 3 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0014 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0016 | 0/0 | 3407 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0017 | 0/0 | 3405 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0018 | 0/0 | 3407 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0019 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0022 | 0/0 | 3407 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0001t0025 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0002t0001 | 0/0 | 3407 | 42 | 3 | 4 | 26 | 1 | 8 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0002t0002 | 0/0 | 3407 | 3 | 0 | 2 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0002t0003 | 0/0 | 3405 | 15 | 1 | 4 | 1 | 0 | 9 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0002t0005 | 1/0 | 3405 | 6 | 0 | 0 | 0 | 1 | 4 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0002t0007 | 0/0 | 3407 | 5 | 0 | 4 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0002t0009 | 0/0 | 3407 | 3 | 0 | 3 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0002t0021 | 0/0 | 3407 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0002t0024 | 0/0 | 3405 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0003t0001 | 0/0 | 3407 | 8 | 0 | 0 | 8 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0003t0002 | 0/0 | 3407 | 39 | 0 | 5 | 33 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0003t0003 | 0/0 | 3405 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0003t0004 | 0/0 | 3405 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0003t0007 | 0/0 | 3407 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0003t0010 | 0/0 | 3407 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0003t0013 | 0/0 | 3407 | 3 | 0 | 0 | 3 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0004t0001 | 0/0 | 3407 | 6 | 0 | 0 | 3 | 0 | 3 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0004t0002 | 0/0 | 3407 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0004t0003 | 0/0 | 3405 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0004t0004 | 0/0 | 3405 | 4 | 0 | 0 | 4 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0004t0011 | 0/0 | 3407 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0004t0014 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0004t0015 | 0/0 | 3405 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0005t0001 | 0/0 | 3407 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0005t0003 | 0/0 | 3405 | 5 | 5 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0005t0004 | 0/0 | 3405 | 4 | 4 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0005t0006 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0005t0020 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0007t0001 | 0/0 | 3407 | 5 | 0 | 0 | 4 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0007t0003 | 0/0 | 3405 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0007t0005 | 0/0 | 3405 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0007t0010 | 0/0 | 3407 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0010t0003 | 0/0 | 3405 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0010t0023 | 0/0 | 3405 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0013t0016 | 0/0 | 3407 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0016t0001 | 0/0 | 3407 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0001c0017t0005 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0018t0006 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0001c0020t0003 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0002c0006t0001 | 0/0 | 3407 | 5 | 0 | 4 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0002c0006t0002 | 0/0 | 3407 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0002c0006t0003 | 0/0 | 3405 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0002c0006t0004 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0002c0006t0005 | 0/0 | 3405 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0002c0006t0006 | 0/0 | 3405 | 2 | 2 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0002c0008t0001 | 0/0 | 3407 | 3 | 0 | 2 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0002c0008t0003 | 0/0 | 3405 | 2 | 0 | 0 | 0 | 1 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0002c0008t0009 | 0/0 | 3407 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0003c0009t0001 | 0/0 | 3407 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0003c0009t0003 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| a0003c0019t0011 | 0/0 | 3407 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0004c0011t0002 | 0/0 | 3407 | 2 | 0 | 0 | 2 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0005c0012t0001 | 0/0 | 3407 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0006c0015t0001 | 0/0 | 3407 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3402): Show |
chr12 | 124771856 | 124868864 |
| a0007c0014t0004 | 0/0 | 3405 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | CCTGC others(3400): Show |
chr12 | 124771856 | 124868864 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0007g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0007g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0008g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0008g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0008g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0008g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0011g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0012g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0014g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0016g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0017g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0017g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0018g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0019g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0022g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0001t0025g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0005g0032 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0005g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0005g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0005g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0005g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0007g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0007g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0007g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0007g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0009g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0009g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0009g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0021g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0002t0024g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0007g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0007g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0007g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0010g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0010g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0013g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0013g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0003t0013g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0011g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0014g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0015g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0004t0015g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0005t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0005t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0005t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0005t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0005t0003g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0005t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0005t0004g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0005t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0005t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0005t0004g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0005t0006g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0005t0020g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0007t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0007t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0007t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0007t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0007t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0007t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0007t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0007t0010g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0010t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0010t0023g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0013t0016g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0016t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0017t0005g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0018t0006g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0001c0020t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0006t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0006t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0006t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0006t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0006t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0006t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0006t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0006t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0006t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0006t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0006t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0008t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0008t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0008t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0008t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0008t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0002c0008t0009g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0003c0009t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0003c0009t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0003c0019t0011g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0004c0011t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0004c0011t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0005c0012t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0005c0012t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0006c0015t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| a0007c0014t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0005 | g0079 | EUR | GBR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00099 | hp2 | a0002 | c0008 | t0001 | g0009 | EUR | GBR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0081 | EUR | GBR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00140 | hp2 | a0002 | c0008 | t0003 | g0015 | EUR | GBR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0087 | EUR | FIN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0086 | EUR | FIN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00408 | hp1 | a0001 | c0004 | t0004 | g0208 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00408 | hp2 | a0001 | c0007 | t0001 | g0150 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00438 | hp1 | a0001 | c0004 | t0004 | g0230 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00438 | hp2 | a0001 | c0003 | t0002 | g0317 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0136 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0098 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00597 | hp1 | a0001 | c0003 | t0002 | g0212 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00597 | hp2 | a0001 | c0003 | t0007 | g0274 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00621 | hp2 | a0001 | c0003 | t0010 | g0283 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00639 | hp1 | a0001 | c0001 | t0022 | g0109 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00673 | hp2 | a0001 | c0004 | t0002 | g0238 | EAS | CHS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00735 | hp1 | a0002 | c0008 | t0001 | g0005 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00735 | hp2 | a0002 | c0008 | t0001 | g0007 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0075 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0073 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01074 | hp1 | a0002 | c0006 | t0001 | g0013 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01099 | hp1 | a0002 | c0008 | t0009 | g0016 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0085 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01106 | hp1 | a0001 | c0002 | t0009 | g0055 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01109 | hp2 | a0002 | c0006 | t0001 | g0003 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01168 | hp1 | a0001 | c0002 | t0003 | g0076 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01169 | hp1 | a0002 | c0006 | t0001 | g0002 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01169 | hp2 | a0001 | c0002 | t0003 | g0077 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01175 | hp2 | a0001 | c0002 | t0003 | g0070 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01243 | hp1 | a0001 | c0001 | t0016 | g0240 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | PUR | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0088 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0158 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01256 | hp2 | a0002 | c0006 | t0005 | g0018 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01257 | hp2 | a0002 | c0006 | t0001 | g0004 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01258 | hp1 | a0002 | c0006 | t0002 | g0017 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0084 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01358 | hp2 | a0001 | c0003 | t0002 | g0300 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01433 | hp1 | a0001 | c0002 | t0007 | g0201 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01496 | hp1 | a0001 | c0002 | t0009 | g0054 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0056 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01515 | hp1 | a0002 | c0006 | t0003 | g0008 | EUR | IBS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01515 | hp2 | a0002 | c0006 | t0001 | g0006 | EUR | IBS | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01884 | hp1 | a0001 | c0001 | t0017 | g0028 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0037 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01891 | hp1 | a0001 | c0005 | t0003 | g0349 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01928 | hp1 | a0001 | c0002 | t0007 | g0216 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01928 | hp2 | a0001 | c0003 | t0002 | g0299 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01934 | hp1 | a0001 | c0003 | t0002 | g0093 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0057 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0243 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01952 | hp1 | a0001 | c0002 | t0007 | g0289 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01993 | hp2 | a0001 | c0002 | t0007 | g0058 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02015 | hp2 | a0001 | c0001 | t0007 | g0323 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02040 | hp1 | a0001 | c0003 | t0002 | g0131 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02055 | hp1 | a0001 | c0005 | t0006 | g0344 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02055 | hp2 | a0001 | c0004 | t0011 | g0119 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02056 | hp1 | a0001 | c0004 | t0001 | g0181 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0307 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02083 | hp1 | a0001 | c0007 | t0001 | g0107 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02083 | hp2 | a0001 | c0001 | t0007 | g0322 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0213 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02132 | hp2 | a0001 | c0002 | t0021 | g0325 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02135 | hp1 | a0001 | c0003 | t0001 | g0215 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0297 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0331 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0329 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | CDX | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02165 | hp1 | a0004 | c0011 | t0002 | g0250 | EAS | CDX | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02165 | hp2 | a0001 | c0007 | t0003 | g0135 | EAS | CDX | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0127 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0169 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0120 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02273 | hp1 | a0001 | c0003 | t0002 | g0291 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02280 | hp2 | a0001 | c0005 | t0004 | g0347 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02293 | hp1 | a0001 | c0002 | t0009 | g0051 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0060 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0118 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02523 | hp2 | a0001 | c0003 | t0002 | g0066 | EAS | KHV | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02572 | hp1 | a0003 | c0009 | t0003 | g0123 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02602 | hp1 | a0001 | c0002 | t0003 | g0083 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02602 | hp2 | a0001 | c0007 | t0001 | g0090 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02615 | hp1 | a0001 | c0001 | t0025 | g0180 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02615 | hp2 | a0001 | c0001 | t0019 | g0061 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0047 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0327 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02647 | hp1 | a0001 | c0005 | t0003 | g0351 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0217 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02698 | hp1 | a0006 | c0015 | t0001 | g0108 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02698 | hp2 | a0002 | c0008 | t0003 | g0014 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02717 | hp2 | a0001 | c0004 | t0015 | g0044 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0027 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02723 | hp2 | a0002 | c0006 | t0006 | g0011 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02735 | hp2 | a0001 | c0010 | t0003 | g0259 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0178 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02738 | hp2 | a0003 | c0009 | t0001 | g0222 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02809 | hp1 | a0001 | c0005 | t0004 | g0353 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0163 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0155 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0256 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0125 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0046 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0324 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02922 | hp1 | a0001 | c0005 | t0004 | g0348 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02965 | hp1 | a0002 | c0006 | t0004 | g0012 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0260 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02970 | hp1 | a0001 | c0001 | t0011 | g0235 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02970 | hp2 | a0001 | c0005 | t0003 | g0354 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0233 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02976 | hp2 | a0001 | c0013 | t0016 | g0334 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0333 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03041 | hp1 | a0003 | c0019 | t0011 | g0342 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | MSL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03098 | hp2 | a0001 | c0004 | t0014 | g0190 | AFR | MSL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03130 | hp1 | a0001 | c0001 | t0008 | g0330 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03139 | hp2 | a0001 | c0005 | t0020 | g0345 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03195 | hp2 | a0001 | c0005 | t0003 | g0355 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0078 | AFR | MSL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | MSL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03239 | hp1 | a0005 | c0012 | t0001 | g0179 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03239 | hp2 | a0001 | c0002 | t0024 | g0265 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03453 | hp1 | a0001 | c0016 | t0001 | g0021 | AFR | MSL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | MSL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | MSL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | MSL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0151 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03491 | hp1 | a0001 | c0002 | t0005 | g0338 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03491 | hp2 | a0001 | c0002 | t0005 | g0255 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03492 | hp1 | a0001 | c0002 | t0005 | g0336 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03516 | hp1 | a0001 | c0001 | t0012 | g0062 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | ESN | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0225 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0035 | AFR | GWD | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03654 | hp1 | a0001 | c0002 | t0003 | g0122 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03669 | hp1 | a0001 | c0004 | t0003 | g0203 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03669 | hp2 | a0001 | c0004 | t0001 | g0293 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0049 | SAS | STU | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0196 | SAS | STU | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0153 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03710 | hp2 | a0001 | c0004 | t0001 | g0154 | SAS | PJL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0091 | SAS | BEB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03831 | hp2 | a0001 | c0002 | t0005 | g0337 | SAS | BEB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | BEB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0138 | SAS | BEB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0249 | SAS | BEB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG04184 | hp2 | a0001 | c0004 | t0001 | g0102 | SAS | BEB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | STU | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0197 | SAS | STU | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG04204 | hp1 | a0001 | c0007 | t0005 | g0191 | SAS | STU | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG04204 | hp2 | a0005 | c0012 | t0001 | g0113 | SAS | STU | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG04228 | hp1 | a0001 | c0003 | t0002 | g0172 | SAS | STU | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG04228 | hp2 | a0001 | c0002 | t0003 | g0207 | SAS | STU | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18522 | hp1 | a0001 | c0005 | t0003 | g0352 | AFR | YRI | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18612 | hp1 | a0001 | c0007 | t0001 | g0134 | EAS | CHB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18747 | hp2 | a0001 | c0004 | t0004 | g0218 | EAS | CHB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18906 | hp1 | a0001 | c0004 | t0015 | g0059 | AFR | YRI | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | YRI | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18939 | hp2 | a0001 | c0003 | t0002 | g0192 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0268 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18942 | hp1 | a0001 | c0003 | t0002 | g0069 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18944 | hp1 | a0001 | c0007 | t0010 | g0156 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18948 | hp1 | a0001 | c0003 | t0002 | g0149 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18953 | hp1 | a0001 | c0003 | t0002 | g0319 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0320 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18957 | hp1 | a0001 | c0003 | t0002 | g0095 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0295 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18960 | hp1 | a0001 | c0007 | t0001 | g0063 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18963 | hp1 | a0001 | c0003 | t0004 | g0321 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18964 | hp1 | a0001 | c0003 | t0002 | g0247 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18965 | hp1 | a0001 | c0004 | t0004 | g0195 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18965 | hp2 | a0001 | c0003 | t0002 | g0231 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18966 | hp1 | a0001 | c0003 | t0010 | g0278 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18966 | hp2 | a0001 | c0003 | t0013 | g0308 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18969 | hp1 | a0001 | c0003 | t0002 | g0110 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0285 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18970 | hp2 | a0001 | c0003 | t0002 | g0129 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18971 | hp2 | a0001 | c0003 | t0013 | g0276 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18974 | hp1 | a0001 | c0003 | t0007 | g0245 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18974 | hp2 | a0001 | c0003 | t0003 | g0137 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18975 | hp2 | a0001 | c0003 | t0002 | g0214 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18981 | hp2 | a0001 | c0003 | t0001 | g0262 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18983 | hp1 | a0004 | c0011 | t0002 | g0210 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18983 | hp2 | a0001 | c0004 | t0001 | g0099 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18985 | hp2 | a0001 | c0003 | t0002 | g0261 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18992 | hp1 | a0001 | c0003 | t0002 | g0263 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18992 | hp2 | a0001 | c0003 | t0001 | g0296 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18994 | hp1 | a0001 | c0003 | t0002 | g0188 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18995 | hp2 | a0001 | c0003 | t0002 | g0100 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19000 | hp1 | a0001 | c0004 | t0001 | g0277 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19001 | hp1 | a0001 | c0003 | t0002 | g0315 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19003 | hp1 | a0001 | c0004 | t0002 | g0271 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19005 | hp2 | a0001 | c0003 | t0002 | g0280 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19007 | hp1 | a0001 | c0003 | t0002 | g0187 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19009 | hp1 | a0001 | c0003 | t0002 | g0160 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19010 | hp1 | a0001 | c0003 | t0007 | g0082 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0139 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19012 | hp1 | a0001 | c0003 | t0002 | g0182 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | LWK | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | LWK | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | LWK | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19056 | hp2 | a0001 | c0003 | t0002 | g0264 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19070 | hp1 | a0001 | c0002 | t0007 | g0309 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19070 | hp2 | a0001 | c0003 | t0002 | g0313 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19077 | hp1 | a0001 | c0003 | t0013 | g0339 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19077 | hp2 | a0001 | c0003 | t0002 | g0275 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19078 | hp2 | a0001 | c0003 | t0002 | g0167 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19080 | hp1 | a0001 | c0003 | t0002 | g0273 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19084 | hp1 | a0001 | c0003 | t0002 | g0064 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0103 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0350 | AFR | YRI | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA19240 | hp2 | a0001 | c0020 | t0003 | g0343 | AFR | YRI | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ASW | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA20129 | hp2 | a0001 | c0018 | t0006 | g0340 | AFR | ASW | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | GIH | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA20905 | hp2 | a0001 | c0010 | t0023 | g0166 | SAS | GIH | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG01123 | hp2 | a0001 | c0001 | t0018 | g0071 | AMR | CLM | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02109 | hp1 | a0001 | c0001 | t0017 | g0030 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02109 | hp2 | a0001 | c0017 | t0005 | g0341 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02486 | hp1 | a0001 | c0005 | t0004 | g0346 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG02559 | hp2 | a0002 | c0006 | t0006 | g0010 | AFR | ACB | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG03471 | hp2 | a0007 | c0014 | t0004 | g0033 | AFR | MSL | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0126 | AFR | USA | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0164 | AFR | USA | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | USA | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | USA | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0148 | REF | REF | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0005 | g0032 | REF | REF | SCARB1_chr12_124771856_124868864 | SCARB1 | chr12 | 124771856 | 124868864 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:124782783 | C | A | 1 | a0006 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.1430G>T | p.Ser477Ile | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/13 | 1574/3405 | 1430/1530 | 477/509 | chr12 | 124782783 | |||
| chr12:124807779 | C | T | 1 | a0007 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.991G>A | p.Val331Ile | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/13 | 1135/3405 | 991/1530 | 331/509 | chr12 | 124807779 | |||
| chr12:124811911 | T | C | 1 | a0004 | 2 | HG02165.hp1 NA18983.hp1 |
missense_variant | MODERATE | c.685A>G | p.Ser229Gly | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/13 | 829/3405 | 685/1530 | 229/509 | chr12 | 124811911 | |||
| chr12:124814996 | C | T | 1 | a0003 | 3 | HG02572.hp1 HG02738.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.403G>A | p.Val135Ile | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 3/13 | 547/3405 | 403/1530 | 135/509 | chr12 | 124814996 | |||
| chr12:124815013 | G | A | 1 | a0005 | 2 | HG03239.hp1 HG04204.hp2 |
missense_variant | MODERATE | c.386C>T | p.Ser129Leu | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 3/13 | 530/3405 | 386/1530 | 129/509 | chr12 | 124815013 | |||
| chr12:124863717 | C | T | 1 | a0002 | 17 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(14): Show |
missense_variant | MODERATE | c.4G>A | p.Gly2Ser | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/13 | 148/3405 | 4/1530 | 2/509 | chr12 | 124863717 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:124800202 | A | G | 14 | a0001c0001 a0001c0003 a0001c0004 others(11): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
synonymous_variant | LOW | c.1050T>C | p.Ala350Ala | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/13 | 1194/3405 | 1050/1530 | 350/509 | chr12 | 124800202 | |||
| chr12:124807837 | C | T | 1 | a0001c0013 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.933G>A | p.Gly311Gly | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/13 | 1077/3405 | 933/1530 | 311/509 | chr12 | 124807837 | |||
| chr12:124807867 | G | A | 1 | a0001c0004 | 17 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(14): Show |
synonymous_variant | LOW | c.903C>T | p.Phe301Phe | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/13 | 1047/3405 | 903/1530 | 301/509 | chr12 | 124807867 | |||
| chr12:124810185 | C | T | 1 | a0001c0010 | 2 | HG02735.hp2 NA20905.hp2 |
synonymous_variant | LOW | c.831G>A | p.Pro277Pro | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/13 | 975/3405 | 831/1530 | 277/509 | chr12 | 124810185 | |||
| chr12:124814331 | G | A | 3 | a0001c0003 a0001c0007 a0004c0011 |
67 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(64): Show |
synonymous_variant | LOW | c.501C>T | p.Gly167Gly | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/13 | 645/3405 | 501/1530 | 167/509 | chr12 | 124814331 | |||
| chr12:124817606 | G | A | 1 | a0001c0016 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.228C>T | p.Ser76Ser | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/13 | 372/3405 | 228/1530 | 76/509 | chr12 | 124817606 | |||
| chr12:124863658 | G | A | 2 | a0001c0017 a0001c0018 |
2 | HG02109.hp2 NA20129.hp2 |
synonymous_variant | LOW | c.63C>T | p.Cys21Cys | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/13 | 207/3405 | 63/1530 | 21/509 | chr12 | 124863658 | |||
| chr12:124863709 | G | A | 3 | a0001c0005 a0001c0020 a0003c0019 |
14 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(11): Show |
synonymous_variant | LOW | c.12C>T | p.Ser4Ser | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/13 | 156/3405 | 12/1530 | 4/509 | chr12 | 124863709 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:124776895 | G | A | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(32): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*1692C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 5788 | chr12 | 124776895 | ||||||
| chr12:124776985 | A | AGG | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(32): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*1600_*1601dupCC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 5697 | chr12 | 124776985 | ||||||
| chr12:124777047 | C | T | 22 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(19): Show |
161 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*1540G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 5636 | chr12 | 124777047 | ||||||
| chr12:124777225 | C | T | 7 | a0001c0001t0004 a0001c0003t0004 a0001c0004t0004 others(4): Show |
21 | HG00408.hp1 HG00438.hp1 HG01109.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1362G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 5458 | chr12 | 124777225 | ||||||
| chr12:124777251 | G | A | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(32): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*1336C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 5432 | chr12 | 124777251 | ||||||
| chr12:124777267 | C | T | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(32): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*1320G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 5416 | chr12 | 124777267 | ||||||
| chr12:124777293 | T | C | 64 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(61): Show |
338 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*1294A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 5390 | chr12 | 124777293 | ||||||
| chr12:124777363 | G | A | 2 | a0001c0001t0016 a0001c0013t0016 |
2 | HG01243.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1224C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 5320 | chr12 | 124777363 | ||||||
| chr12:124777558 | G | A | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(32): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*1029C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 5125 | chr12 | 124777558 | ||||||
| chr12:124777593 | G | A | 1 | a0001c0001t0022 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*994C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 5090 | chr12 | 124777593 | ||||||
| chr12:124777708 | A | G | 1 | a0001c0001t0012 | 3 | HG02451.hp1 HG03209.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*879T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4975 | chr12 | 124777708 | ||||||
| chr12:124777770 | C | T | 2 | a0001c0003t0010 a0001c0007t0010 |
3 | HG00621.hp2 NA18944.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*817G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4913 | chr12 | 124777770 | ||||||
| chr12:124777773 | C | T | 1 | a0001c0002t0021 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*814G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4910 | chr12 | 124777773 | ||||||
| chr12:124777779 | C | G | 4 | a0001c0001t0006 a0001c0005t0006 a0001c0018t0006 others(1): Show |
12 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*808G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4904 | chr12 | 124777779 | ||||||
| chr12:124777827 | G | A | 1 | a0001c0010t0023 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*760C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4856 | chr12 | 124777827 | ||||||
| chr12:124777842 | G | A | 1 | a0001c0002t0024 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*745C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4841 | chr12 | 124777842 | ||||||
| chr12:124777963 | G | A | 6 | a0001c0001t0006 a0001c0001t0025 a0001c0004t0015 others(3): Show |
15 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*624C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4720 | chr12 | 124777963 | ||||||
| chr12:124777967 | G | A | 1 | a0001c0001t0019 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*620C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4716 | chr12 | 124777967 | ||||||
| chr12:124777970 | G | T | 2 | a0001c0002t0009 a0002c0008t0009 |
4 | HG01099.hp1 HG01106.hp1 HG01496.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*617C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4713 | chr12 | 124777970 | ||||||
| chr12:124777986 | G | A | 1 | a0001c0003t0013 | 3 | NA18966.hp2 NA18971.hp2 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*601C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4697 | chr12 | 124777986 | ||||||
| chr12:124778007 | T | C | 2 | a0001c0001t0016 a0001c0013t0016 |
2 | HG01243.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*580A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4676 | chr12 | 124778007 | ||||||
| chr12:124778019 | A | G | 1 | a0001c0005t0020 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4664 | chr12 | 124778019 | ||||||
| chr12:124778029 | G | A | 1 | a0001c0001t0017 | 2 | HG01884.hp1 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*558C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4654 | chr12 | 124778029 | ||||||
| chr12:124778104 | T | C | 1 | a0001c0001t0025 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*483A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4579 | chr12 | 124778104 | ||||||
| chr12:124778233 | G | T | 1 | a0001c0001t0019 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*354C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4450 | chr12 | 124778233 | ||||||
| chr12:124778291 | G | T | 1 | a0001c0001t0018 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*296C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4392 | chr12 | 124778291 | ||||||
| chr12:124778493 | C | T | 6 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0014 others(3): Show |
14 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*94G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4190 | chr12 | 124778493 | ||||||
| chr12:124778515 | C | T | 11 | a0001c0001t0002 a0001c0001t0007 a0001c0002t0002 others(8): Show |
77 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*72G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 13/13 | 4168 | chr12 | 124778515 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:124778658 | A | C | 338 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(335): Show |
339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.*1-72T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124778658 | |||||||
| chr12:124778698 | G | A | 9 | a0001c0001t0008g0027 a0001c0001t0008g0036 a0001c0001t0008g0037 others(6): Show |
9 | HG01884.hp2 HG02145.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.*1-112C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124778698 | |||||||
| chr12:124778729 | G | A | 2 | a0001c0001t0016g0240 a0001c0013t0016g0334 |
2 | HG01243.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.*1-143C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124778729 | |||||||
| chr12:124778952 | A | G | 1 | a0001c0001t0003g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.*1-366T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124778952 | |||||||
| chr12:124778982 | T | C | 1 | a0001c0003t0002g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.*1-396A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124778982 | |||||||
| chr12:124779005 | C | T | 21 | a0001c0001t0004g0026 a0001c0001t0004g0042 a0001c0001t0004g0048 others(18): Show |
21 | HG00408.hp1 HG00438.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.*1-419G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779005 | |||||||
| chr12:124779034 | T | C | 13 | a0001c0001t0006g0022 a0001c0001t0006g0024 a0001c0001t0006g0031 others(10): Show |
13 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.*1-448A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779034 | |||||||
| chr12:124779068 | G | A | 1 | a0001c0001t0019g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*1-482C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779068 | |||||||
| chr12:124779083 | C | T | 1 | a0001c0002t0003g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*1-497G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779083 | |||||||
| chr12:124779113 | C | T | 2 | a0001c0001t0014g0127 a0001c0004t0014g0190 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.*1-527G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779113 | |||||||
| chr12:124779436 | G | A | 1 | a0001c0001t0011g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.*1-850C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779436 | |||||||
| chr12:124779472 | A | G | 341 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(338): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.*1-886T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779472 | |||||||
| chr12:124779621 | G | C | 1 | a0001c0001t0019g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.*1-1035C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779621 | |||||||
| chr12:124779646 | T | G | 1 | a0001c0001t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*1-1060A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779646 | |||||||
| chr12:124779717 | T | C | 3 | a0001c0001t0003g0038 a0001c0001t0003g0224 a0001c0001t0003g0239 |
3 | HG01361.hp1 HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.*1-1131A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779717 | |||||||
| chr12:124779733 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.*1-1147C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779733 | |||||||
| chr12:124779741 | T | G | 162 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(159): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.*1-1155A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779741 | |||||||
| chr12:124779747 | G | A | 120 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0040 others(117): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.*1-1161C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779747 | |||||||
| chr12:124779850 | G | A | 1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*1-1264C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779850 | |||||||
| chr12:124779901 | C | T | 1 | a0001c0001t0011g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.*1-1315G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124779901 | |||||||
| chr12:124780022 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.*1-1436C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780022 | |||||||
| chr12:124780040 | T | G | 2 | a0001c0004t0015g0044 a0001c0004t0015g0059 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*1-1454A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780040 | |||||||
| chr12:124780074 | C | T | 13 | a0001c0001t0003g0025 a0001c0001t0003g0161 a0001c0001t0003g0165 others(10): Show |
13 | HG01891.hp1 HG02055.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.*1-1488G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780074 | |||||||
| chr12:124780141 | T | A | 1 | a0001c0003t0001g0215 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.*1-1555A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780141 | |||||||
| chr12:124780583 | T | C | 2 | a0001c0001t0004g0121 a0001c0017t0005g0341 |
2 | HG02109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.*1-1997A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780583 | |||||||
| chr12:124780655 | G | A | 117 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0052 others(114): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.1530+2028C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780655 | |||||||
| chr12:124780667 | G | A | 2 | a0001c0004t0015g0044 a0001c0004t0015g0059 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1530+2016C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780667 | |||||||
| chr12:124780729 | A | C | 1 | a0001c0001t0006g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1530+1954T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780729 | |||||||
| chr12:124780886 | C | T | 1 | a0002c0008t0003g0015 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1530+1797G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780886 | |||||||
| chr12:124780946 | C | T | 1 | a0001c0001t0014g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1530+1737G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780946 | |||||||
| chr12:124780950 | G | A | 1 | a0001c0001t0014g0127 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1530+1733C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780950 | |||||||
| chr12:124780961 | G | A | 83 | a0001c0001t0002g0065 a0001c0001t0002g0096 a0001c0001t0002g0104 others(80): Show |
83 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.1530+1722C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780961 | |||||||
| chr12:124780974 | C | T | 31 | a0001c0001t0003g0025 a0001c0001t0003g0161 a0001c0001t0003g0165 others(28): Show |
31 | HG00408.hp1 HG00438.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1530+1709G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124780974 | |||||||
| chr12:124781090 | A | G | 297 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(294): Show |
298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.1530+1593T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781090 | |||||||
| chr12:124781165 | G | A | 1 | a0001c0003t0002g0315 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1530+1518C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781165 | |||||||
| chr12:124781354 | C | T | 1 | a0001c0002t0001g0303 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1530+1329G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781354 | |||||||
| chr12:124781413 | A | G | 11 | a0001c0001t0002g0305 a0001c0001t0003g0068 a0001c0001t0003g0140 others(8): Show |
11 | HG02015.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.1530+1270T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781413 | |||||||
| chr12:124781427 | G | C | 233 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(230): Show |
233 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1530+1256C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781427 | |||||||
| chr12:124781428 | G | A | 70 | a0001c0001t0002g0065 a0001c0001t0002g0096 a0001c0001t0002g0104 others(67): Show |
70 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1530+1255C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781428 | |||||||
| chr12:124781578 | G | A | 1 | a0001c0002t0001g0311 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1530+1105C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781578 | |||||||
| chr12:124781680 | G | A | 1 | a0001c0001t0005g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1530+1003C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781680 | |||||||
| chr12:124781696 | C | T | 2 | a0001c0001t0001g0185 a0001c0002t0001g0081 |
2 | HG00140.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1530+987G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781696 | |||||||
| chr12:124781775 | G | GTTTGTTT others(23): Show |
4 | a0001c0002t0009g0051 a0001c0002t0009g0054 a0001c0002t0009g0055 others(1): Show |
4 | HG01099.hp1 HG01106.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1530+878_1530+907d others(32): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781775 | |||||||
| chr12:124781832 | C | G | 1 | a0001c0002t0001g0252 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1530+851G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781832 | |||||||
| chr12:124781886 | T | C | 81 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0111 others(78): Show |
82 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1530+797A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781886 | |||||||
| chr12:124781928 | C | T | 1 | a0001c0003t0002g0315 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1530+755G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781928 | |||||||
| chr12:124781929 | G | A | 5 | a0001c0001t0008g0046 a0001c0001t0008g0330 a0001c0001t0008g0331 others(2): Show |
5 | HG02145.hp1 HG02257.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1530+754C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124781929 | |||||||
| chr12:124782009 | G | A | 1 | a0002c0006t0004g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1530+674C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782009 | |||||||
| chr12:124782046 | C | A | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1530+637G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782046 | |||||||
| chr12:124782071 | A | C | 183 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(180): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1530+612T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782071 | |||||||
| chr12:124782072 | A | T | 1 | a0001c0003t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1530+611T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782072 | |||||||
| chr12:124782264 | T | G | 2 | a0001c0004t0015g0044 a0001c0004t0015g0059 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1530+419A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782264 | |||||||
| chr12:124782316 | A | G | 1 | a0002c0006t0004g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1530+367T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782316 | |||||||
| chr12:124782367 | G | T | 70 | a0001c0001t0002g0065 a0001c0001t0002g0096 a0001c0001t0002g0104 others(67): Show |
70 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1530+316C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782367 | |||||||
| chr12:124782537 | T | C | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1530+146A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782537 | |||||||
| chr12:124782540 | A | G | 5 | a0001c0001t0005g0045 a0001c0001t0008g0036 a0001c0001t0008g0037 others(2): Show |
5 | HG01884.hp2 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1530+143T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782540 | |||||||
| chr12:124782605 | C | T | 2 | a0001c0001t0012g0060 a0001c0001t0012g0062 |
2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1530+78G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782605 | |||||||
| chr12:124782622 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1530+61C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782622 | |||||||
| chr12:124782634 | C | T | 4 | a0001c0001t0006g0022 a0001c0001t0006g0024 a0001c0001t0006g0031 others(1): Show |
4 | HG01243.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1530+49G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782634 | |||||||
| chr12:124782655 | G | A | 2 | a0001c0002t0001g0252 a0001c0002t0001g0304 |
2 | HG02027.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1530+28C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 12/12 | chr12 | 124782655 | |||||||
| chr12:124782873 | G | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0281 |
2 | NA18982.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1402-62C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124782873 | |||||||
| chr12:124782955 | G | A | 5 | a0001c0001t0005g0045 a0001c0001t0008g0036 a0001c0001t0008g0037 others(2): Show |
5 | HG01884.hp2 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-144C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124782955 | |||||||
| chr12:124782977 | G | A | 4 | a0001c0003t0004g0321 a0001c0004t0004g0208 a0001c0004t0004g0218 others(1): Show |
4 | HG00408.hp1 HG00438.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402-166C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124782977 | |||||||
| chr12:124783167 | G | A | 1 | a0001c0002t0001g0332 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1402-356C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124783167 | |||||||
| chr12:124783432 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1402-621G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124783432 | |||||||
| chr12:124783440 | AT | A | 13 | a0001c0001t0001g0223 a0001c0001t0001g0270 a0001c0001t0002g0234 others(10): Show |
13 | HG01243.hp2 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1402-630delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124783440 | |||||||
| chr12:124783653 | A | G | 164 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(161): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1402-842T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124783653 | |||||||
| chr12:124783659 | C | T | 5 | a0001c0001t0011g0235 a0001c0001t0017g0028 a0001c0004t0015g0044 others(2): Show |
5 | HG01884.hp1 HG02717.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1402-848G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124783659 | |||||||
| chr12:124783661 | GGAGGCT | G | 4 | a0001c0001t0003g0239 a0001c0001t0005g0043 a0001c0001t0005g0047 others(1): Show |
4 | HG01943.hp1 HG02622.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402-856_1402-851d others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124783661 | |||||||
| chr12:124783661 | GGAGGCTG others(11): Show |
G | 12 | a0001c0001t0004g0026 a0001c0001t0004g0042 a0001c0001t0004g0124 others(9): Show |
12 | HG01109.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1402-868_1402-851d others(20): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124783661 | |||||||
| chr12:124783695 | A | G | 164 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(161): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1402-884T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124783695 | |||||||
| chr12:124783791 | C | A | 1 | a0001c0003t0002g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1402-980G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124783791 | |||||||
| chr12:124783835 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1402-1024A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124783835 | |||||||
| chr12:124783886 | G | A | 162 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(159): Show |
162 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.1402-1075C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124783886 | |||||||
| chr12:124783919 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1402-1108A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124783919 | |||||||
| chr12:124784126 | A | C | 4 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0016g0240 others(1): Show |
4 | HG01243.hp1 HG02258.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402-1315T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124784126 | |||||||
| chr12:124784171 | T | C | 1 | a0001c0001t0017g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1402-1360A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124784171 | |||||||
| chr12:124784341 | G | C | 1 | a0001c0002t0001g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1402-1530C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124784341 | |||||||
| chr12:124784367 | A | G | 1 | a0001c0001t0003g0237 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1402-1556T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124784367 | |||||||
| chr12:124784462 | C | T | 1 | a0001c0003t0002g0136 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1402-1651G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124784462 | |||||||
| chr12:124784684 | G | A | 3 | a0001c0001t0017g0030 a0001c0001t0019g0061 a0003c0019t0011g0342 |
3 | HG02109.hp1 HG02615.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1401+1673C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124784684 | |||||||
| chr12:124784689 | C | T | 1 | a0002c0006t0001g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1401+1668G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124784689 | |||||||
| chr12:124784777 | A | C | 178 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(175): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1401+1580T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124784777 | |||||||
| chr12:124784783 | C | T | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1401+1574G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124784783 | |||||||
| chr12:124784929 | T | C | 175 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(172): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.1401+1428A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124784929 | |||||||
| chr12:124784941 | A | ATT | 175 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(172): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.1401+1415_1401+141 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124784941 | |||||||
| chr12:124784950 | C | T | 175 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(172): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.1401+1407G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124784950 | |||||||
| chr12:124785085 | C | T | 1 | a0001c0001t0004g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1401+1272G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124785085 | |||||||
| chr12:124785122 | T | C | 1 | a0001c0001t0005g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1401+1235A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124785122 | |||||||
| chr12:124785146 | G | C | 175 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(172): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.1401+1211C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124785146 | |||||||
| chr12:124785176 | T | G | 1 | a0001c0001t0019g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1401+1181A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124785176 | |||||||
| chr12:124785193 | G | A | 2 | a0001c0004t0015g0044 a0001c0004t0015g0059 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1401+1164C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124785193 | |||||||
| chr12:124785253 | C | G | 180 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(177): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1401+1104G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124785253 | |||||||
| chr12:124785292 | T | C | 1 | a0001c0002t0007g0058 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1401+1065A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124785292 | |||||||
| chr12:124785349 | T | C | 2 | a0001c0001t0019g0061 a0002c0006t0004g0012 |
2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1401+1008A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124785349 | |||||||
| chr12:124785623 | C | T | 2 | a0001c0002t0003g0091 a0001c0002t0003g0249 |
2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1401+734G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124785623 | |||||||
| chr12:124785625 | G | C | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1401+732C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124785625 | |||||||
| chr12:124785796 | T | C | 1 | a0003c0019t0011g0342 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1401+561A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124785796 | |||||||
| chr12:124786050 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1401+307C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124786050 | |||||||
| chr12:124786183 | A | G | 3 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0016g0240 |
3 | HG01243.hp1 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1401+174T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124786183 | |||||||
| chr12:124786224 | G | A | 1 | a0001c0002t0001g0168 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1401+133C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124786224 | |||||||
| chr12:124786227 | A | G | 123 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0301 others(120): Show |
123 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.1401+130T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 11/12 | chr12 | 124786227 | |||||||
| chr12:124786544 | G | C | 123 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0111 others(120): Show |
123 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1255-41C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 10/12 | chr12 | 124786544 | |||||||
| chr12:124786555 | A | C | 67 | a0001c0001t0001g0301 a0001c0001t0001g0318 a0001c0001t0002g0065 others(64): Show |
67 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.1255-52T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 10/12 | chr12 | 124786555 | |||||||
| chr12:124786559 | C | T | 2 | a0001c0003t0002g0103 a0001c0003t0002g0261 |
2 | NA18985.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1255-56G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 10/12 | chr12 | 124786559 | |||||||
| chr12:124786572 | C | T | 8 | a0001c0001t0005g0045 a0001c0001t0008g0036 a0001c0001t0008g0037 others(5): Show |
8 | HG01884.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1255-69G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 10/12 | chr12 | 124786572 | |||||||
| chr12:124786719 | T | C | 1 | a0003c0019t0011g0342 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1255-216A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 10/12 | chr12 | 124786719 | |||||||
| chr12:124786922 | G | C | 2 | a0001c0001t0002g0104 a0001c0001t0002g0221 |
2 | HG00673.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1255-419C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 10/12 | chr12 | 124786922 | |||||||
| chr12:124787063 | T | C | 1 | a0001c0001t0003g0246 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1254+343A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 10/12 | chr12 | 124787063 | |||||||
| chr12:124787065 | A | G | 1 | a0001c0003t0001g0262 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1254+341T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 10/12 | chr12 | 124787065 | |||||||
| chr12:124787132 | C | T | 81 | a0001c0001t0001g0301 a0001c0001t0001g0318 a0001c0001t0002g0065 others(78): Show |
81 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1254+274G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 10/12 | chr12 | 124787132 | |||||||
| chr12:124787186 | C | G | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1254+220G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 10/12 | chr12 | 124787186 | |||||||
| chr12:124787292 | T | C | 1 | a0001c0004t0014g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1254+114A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 10/12 | chr12 | 124787292 | |||||||
| chr12:124787507 | C | G | 1 | a0001c0001t0019g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1203-50G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124787507 | |||||||
| chr12:124787562 | C | T | 1 | a0001c0001t0008g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1203-105G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124787562 | |||||||
| chr12:124787598 | C | T | 1 | a0001c0003t0001g0262 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1203-141G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124787598 | |||||||
| chr12:124787602 | A | T | 1 | a0001c0003t0001g0262 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1203-145T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124787602 | |||||||
| chr12:124787694 | A | T | 1 | a0001c0004t0002g0271 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1203-237T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124787694 | |||||||
| chr12:124787712 | GT | G | 24 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0038 others(21): Show |
24 | HG00408.hp1 HG00438.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1203-256delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124787712 | |||||||
| chr12:124787714 | T | G | 1 | a0001c0003t0002g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1203-257A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124787714 | |||||||
| chr12:124787723 | T | A | 24 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0038 others(21): Show |
24 | HG00408.hp1 HG00438.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1203-266A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124787723 | |||||||
| chr12:124787724 | C | A | 24 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0038 others(21): Show |
24 | HG00408.hp1 HG00438.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1203-267G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124787724 | |||||||
| chr12:124787972 | T | G | 1 | a0001c0003t0001g0262 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1203-515A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124787972 | |||||||
| chr12:124788217 | A | T | 134 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0301 others(131): Show |
134 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1203-760T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124788217 | |||||||
| chr12:124788440 | G | A | 1 | a0001c0004t0001g0099 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1203-983C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124788440 | |||||||
| chr12:124788497 | T | C | 24 | a0001c0001t0003g0161 a0001c0001t0003g0165 a0001c0001t0003g0169 others(21): Show |
24 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1203-1040A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124788497 | |||||||
| chr12:124788770 | T | C | 5 | a0001c0001t0005g0045 a0001c0001t0008g0036 a0001c0001t0008g0037 others(2): Show |
5 | HG01884.hp2 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203-1313A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124788770 | |||||||
| chr12:124788791 | C | T | 5 | a0001c0001t0003g0161 a0001c0001t0003g0165 a0001c0005t0003g0349 others(2): Show |
5 | HG01891.hp1 HG02647.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203-1334G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124788791 | |||||||
| chr12:124788792 | G | T | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1203-1335C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124788792 | |||||||
| chr12:124788833 | A | G | 1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1203-1376T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124788833 | |||||||
| chr12:124788957 | C | G | 1 | a0001c0001t0003g0232 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1203-1500G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124788957 | |||||||
| chr12:124788995 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1203-1538G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124788995 | |||||||
| chr12:124789014 | A | C | 1 | a0001c0003t0001g0262 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1203-1557T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789014 | |||||||
| chr12:124789113 | A | T | 135 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0301 others(132): Show |
135 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1203-1656T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789113 | |||||||
| chr12:124789121 | T | C | 135 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0301 others(132): Show |
135 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1203-1664A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789121 | |||||||
| chr12:124789196 | G | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0038 others(12): Show |
15 | HG01081.hp2 HG01123.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1203-1739C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789196 | |||||||
| chr12:124789197 | G | A | 1 | a0001c0001t0008g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1203-1740C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789197 | |||||||
| chr12:124789208 | A | G | 93 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0301 others(90): Show |
93 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1203-1751T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789208 | |||||||
| chr12:124789221 | C | T | 135 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0301 others(132): Show |
135 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.1203-1764G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789221 | |||||||
| chr12:124789238 | C | T | 2 | a0001c0002t0001g0151 a0001c0002t0005g0255 |
2 | HG03490.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1203-1781G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789238 | |||||||
| chr12:124789312 | T | A | 1 | a0001c0003t0001g0262 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1203-1855A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789312 | |||||||
| chr12:124789402 | TAAG | T | 3 | a0001c0001t0017g0030 a0001c0004t0011g0119 a0002c0006t0004g0012 |
3 | HG02055.hp2 HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1203-1948_1203-194 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789402 | |||||||
| chr12:124789412 | G | A | 1 | a0001c0001t0019g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1203-1955C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789412 | |||||||
| chr12:124789454 | C | T | 1 | a0002c0008t0001g0007 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1203-1997G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789454 | |||||||
| chr12:124789473 | A | C | 1 | a0001c0004t0014g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1203-2016T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789473 | |||||||
| chr12:124789495 | A | C | 1 | a0001c0003t0001g0262 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1203-2038T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789495 | |||||||
| chr12:124789560 | A | G | 1 | a0001c0001t0005g0243 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1203-2103T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789560 | |||||||
| chr12:124789627 | CG | C | 6 | a0001c0001t0002g0221 a0001c0001t0005g0045 a0001c0001t0008g0036 others(3): Show |
6 | HG01884.hp2 HG02976.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203-2171delC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789627 | |||||||
| chr12:124789734 | G | A | 1 | a0002c0006t0004g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1203-2277C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789734 | |||||||
| chr12:124789778 | C | T | 1 | a0002c0006t0006g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1203-2321G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789778 | |||||||
| chr12:124789779 | G | T | 1 | a0001c0003t0001g0262 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1203-2322C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789779 | |||||||
| chr12:124789826 | C | G | 1 | a0001c0002t0001g0049 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1203-2369G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789826 | |||||||
| chr12:124789849 | A | G | 14 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0038 others(11): Show |
14 | HG01081.hp2 HG01123.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1203-2392T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789849 | |||||||
| chr12:124789861 | A | T | 1 | a0001c0003t0001g0262 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1203-2404T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789861 | |||||||
| chr12:124789881 | C | T | 1 | a0001c0001t0019g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1203-2424G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789881 | |||||||
| chr12:124789984 | C | T | 10 | a0001c0004t0001g0099 a0001c0004t0001g0154 a0001c0004t0001g0277 others(7): Show |
10 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.1203-2527G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789984 | |||||||
| chr12:124789988 | C | T | 8 | a0001c0001t0002g0128 a0001c0001t0005g0084 a0001c0002t0005g0079 others(5): Show |
8 | HG00099.hp1 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1203-2531G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789988 | |||||||
| chr12:124789991 | C | A | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1203-2534G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124789991 | |||||||
| chr12:124790009 | C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0040 a0001c0001t0005g0084 a0001c0002t0005g0079 others(5): Show |
8 | HG00099.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1203-2560_1203-255 others(12): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790009 | |||||||
| chr12:124790009 | C | CAAAAAAA others(2): Show |
23 | a0001c0001t0001g0111 a0001c0001t0003g0038 a0001c0001t0003g0117 others(20): Show |
23 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1203-2561_1203-255 others(13): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790009 | |||||||
| chr12:124790009 | C | CAAAAAAA others(3): Show |
9 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0016g0240 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1203-2562_1203-255 others(14): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790009 | |||||||
| chr12:124790009 | C | CAAAAAAA others(4): Show |
70 | a0001c0001t0001g0301 a0001c0001t0001g0318 a0001c0001t0002g0065 others(67): Show |
70 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1203-2563_1203-255 others(15): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790009 | |||||||
| chr12:124790009 | C | CAAAAAAA others(5): Show |
23 | a0001c0001t0003g0161 a0001c0001t0003g0165 a0001c0001t0003g0226 others(20): Show |
23 | HG00544.hp1 HG01358.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1203-2564_1203-255 others(16): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790009 | |||||||
| chr12:124790009 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0006g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1203-2565_1203-255 others(17): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790009 | |||||||
| chr12:124790097 | A | T | 1 | a0001c0003t0001g0262 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1203-2640T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790097 | |||||||
| chr12:124790104 | G | A | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1203-2647C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790104 | |||||||
| chr12:124790377 | T | TCAACAA | 13 | a0001c0001t0002g0128 a0001c0001t0005g0045 a0001c0001t0005g0084 others(10): Show |
13 | HG00099.hp1 HG01256.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1203-2926_1203-292 others(10): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790377 | |||||||
| chr12:124790377 | T | TCAACAAC others(5): Show |
10 | a0001c0004t0001g0099 a0001c0004t0001g0154 a0001c0004t0001g0277 others(7): Show |
10 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.1203-2932_1203-292 others(16): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790377 | |||||||
| chr12:124790435 | A | C | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1203-2978T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790435 | |||||||
| chr12:124790505 | A | T | 1 | a0001c0002t0001g0333 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1203-3048T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790505 | |||||||
| chr12:124790698 | A | G | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1203-3241T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790698 | |||||||
| chr12:124790772 | G | A | 18 | a0001c0001t0003g0161 a0001c0001t0003g0165 a0001c0001t0003g0226 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1203-3315C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790772 | |||||||
| chr12:124790836 | G | A | 1 | a0001c0001t0003g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1203-3379C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790836 | |||||||
| chr12:124790868 | T | G | 103 | a0001c0001t0001g0301 a0001c0001t0001g0318 a0001c0001t0002g0065 others(100): Show |
103 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1203-3411A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790868 | |||||||
| chr12:124790886 | G | A | 5 | a0001c0001t0005g0045 a0001c0001t0008g0036 a0001c0001t0008g0037 others(2): Show |
5 | HG01884.hp2 HG02976.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203-3429C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790886 | |||||||
| chr12:124790984 | T | G | 11 | a0001c0004t0001g0099 a0001c0004t0001g0102 a0001c0004t0001g0154 others(8): Show |
11 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.1203-3527A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124790984 | |||||||
| chr12:124791061 | G | C | 1 | a0001c0002t0001g0327 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1203-3604C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791061 | |||||||
| chr12:124791127 | T | C | 9 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0117 others(6): Show |
9 | HG01081.hp2 HG01123.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1203-3670A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791127 | |||||||
| chr12:124791241 | T | C | 15 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0038 others(12): Show |
15 | HG01081.hp2 HG01123.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1203-3784A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791241 | |||||||
| chr12:124791273 | C | T | 1 | a0001c0002t0003g0122 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1203-3816G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791273 | |||||||
| chr12:124791347 | C | A | 3 | a0001c0002t0005g0336 a0001c0002t0005g0337 a0001c0002t0005g0338 |
3 | HG03491.hp1 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1202+3848G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791347 | |||||||
| chr12:124791359 | C | T | 3 | a0001c0001t0017g0030 a0001c0004t0011g0119 a0002c0006t0004g0012 |
3 | HG02055.hp2 HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1202+3836G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791359 | |||||||
| chr12:124791418 | T | C | 1 | a0001c0001t0003g0257 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1202+3777A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791418 | |||||||
| chr12:124791539 | T | C | 8 | a0001c0001t0002g0128 a0001c0001t0005g0084 a0001c0002t0005g0079 others(5): Show |
8 | HG00099.hp1 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1202+3656A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791539 | |||||||
| chr12:124791556 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1202+3639T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791556 | |||||||
| chr12:124791678 | C | T | 1 | a0001c0003t0002g0100 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1202+3517G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791678 | |||||||
| chr12:124791682 | C | T | 9 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0117 others(6): Show |
9 | HG01081.hp2 HG01123.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202+3513G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791682 | |||||||
| chr12:124791685 | A | G | 347 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(344): Show |
348 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.1202+3510T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791685 | |||||||
| chr12:124791708 | G | A | 2 | a0001c0004t0015g0044 a0001c0004t0015g0059 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1202+3487C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791708 | |||||||
| chr12:124791720 | GCTGAGGC others(1730): Show |
G | 1 | a0001c0001t0003g0232 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1202+1738_1202+347 others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791720 | |||||||
| chr12:124791759 | C | G | 1 | a0001c0004t0001g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1202+3436G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791759 | |||||||
| chr12:124791780 | A | G | 3 | a0001c0001t0017g0030 a0001c0004t0011g0119 a0002c0006t0004g0012 |
3 | HG02055.hp2 HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1202+3415T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791780 | |||||||
| chr12:124791817 | G | A | 3 | a0001c0001t0017g0030 a0001c0004t0011g0119 a0002c0006t0004g0012 |
3 | HG02055.hp2 HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1202+3378C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791817 | |||||||
| chr12:124791911 | G | A | 6 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0016g0240 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1202+3284C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791911 | |||||||
| chr12:124791966 | A | G | 3 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0016g0240 |
3 | HG01243.hp1 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1202+3229T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124791966 | |||||||
| chr12:124792128 | A | G | 1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1202+3067T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792128 | |||||||
| chr12:124792197 | G | A | 8 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0005g0045 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1202+2998C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792197 | |||||||
| chr12:124792226 | G | A | 5 | a0001c0001t0003g0117 a0001c0001t0003g0239 a0001c0001t0005g0043 others(2): Show |
5 | HG01943.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1202+2969C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792226 | |||||||
| chr12:124792360 | G | A | 1 | a0001c0001t0017g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1202+2835C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792360 | |||||||
| chr12:124792380 | G | A | 4 | a0001c0002t0009g0051 a0001c0002t0009g0054 a0001c0002t0009g0055 others(1): Show |
4 | HG01099.hp1 HG01106.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+2815C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792380 | |||||||
| chr12:124792423 | G | A | 13 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(10): Show |
14 | HG00280.hp1 HG00735.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.1202+2772C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792423 | |||||||
| chr12:124792459 | G | A | 3 | a0001c0001t0017g0030 a0001c0004t0011g0119 a0002c0006t0004g0012 |
3 | HG02055.hp2 HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1202+2736C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792459 | |||||||
| chr12:124792588 | A | G | 135 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0258 others(132): Show |
135 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1202+2607T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792588 | |||||||
| chr12:124792721 | C | CA | 31 | a0001c0001t0001g0185 a0001c0001t0002g0104 a0001c0001t0002g0157 others(28): Show |
31 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1202+2473dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792721 | |||||||
| chr12:124792721 | CA | C | 22 | a0001c0001t0001g0270 a0001c0001t0001g0281 a0001c0001t0002g0221 others(19): Show |
22 | HG01070.hp1 HG01256.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.1202+2473delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792721 | |||||||
| chr12:124792767 | TA | T | 3 | a0001c0001t0001g0223 a0001c0002t0001g0256 a0001c0020t0003g0343 |
3 | HG02559.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1202+2427delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792767 | |||||||
| chr12:124792777 | T | C | 130 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0301 others(127): Show |
130 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1202+2418A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792777 | |||||||
| chr12:124792852 | G | A | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1202+2343C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792852 | |||||||
| chr12:124792914 | G | A | 5 | a0001c0001t0001g0130 a0001c0002t0001g0133 a0001c0002t0001g0282 others(2): Show |
5 | HG00408.hp2 HG02083.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1202+2281C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792914 | |||||||
| chr12:124792926 | T | TG | 352 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(349): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1202+2268dupC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124792926 | |||||||
| chr12:124793107 | G | A | 4 | a0001c0001t0008g0046 a0001c0001t0008g0330 a0001c0001t0008g0331 others(1): Show |
4 | HG02145.hp1 HG02896.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+2088C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793107 | |||||||
| chr12:124793111 | T | C | 1 | a0001c0001t0012g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1202+2084A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793111 | |||||||
| chr12:124793253 | C | T | 19 | a0001c0001t0003g0161 a0001c0001t0003g0165 a0001c0001t0003g0226 others(16): Show |
19 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1202+1942G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793253 | |||||||
| chr12:124793296 | G | A | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1202+1899C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793296 | |||||||
| chr12:124793425 | T | TG | 352 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(349): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1202+1769dupC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793425 | |||||||
| chr12:124793457 | C | G | 13 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0038 others(10): Show |
13 | HG01081.hp2 HG01123.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.1202+1738G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793457 | |||||||
| chr12:124793457 | C | T | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0005g0057 |
3 | HG01358.hp1 HG01934.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1202+1738G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793457 | |||||||
| chr12:124793490 | G | A | 4 | a0001c0001t0003g0117 a0001c0001t0003g0239 a0001c0001t0005g0043 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202+1705C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793490 | |||||||
| chr12:124793546 | A | G | 1 | a0001c0001t0008g0331 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1202+1649T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793546 | |||||||
| chr12:124793625 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1202+1570C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793625 | |||||||
| chr12:124793656 | G | A | 1 | a0001c0005t0020g0345 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1202+1539C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793656 | |||||||
| chr12:124793685 | T | C | 1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1202+1510A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793685 | |||||||
| chr12:124793692 | C | CA | 25 | a0001c0001t0001g0185 a0001c0001t0002g0229 a0001c0001t0003g0086 others(22): Show |
25 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(22): Show |
intron_variant | MODIFIER | c.1202+1502dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793692 | |||||||
| chr12:124793692 | C | CAA | 8 | a0001c0001t0003g0237 a0001c0001t0005g0045 a0001c0001t0008g0036 others(5): Show |
8 | HG01243.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1202+1501_1202+150 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793692 | |||||||
| chr12:124793692 | C | CAAAA | 11 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0038 others(8): Show |
11 | HG01081.hp2 HG01123.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1202+1499_1202+150 others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793692 | |||||||
| chr12:124793692 | CA | C | 7 | a0001c0001t0001g0034 a0001c0001t0001g0241 a0001c0001t0017g0030 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202+1502delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793692 | |||||||
| chr12:124793739 | G | T | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1202+1456C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793739 | |||||||
| chr12:124793795 | G | A | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1202+1400C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124793795 | |||||||
| chr12:124794092 | G | A | 1 | a0001c0001t0019g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1202+1103C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794092 | |||||||
| chr12:124794101 | G | A | 1 | a0001c0001t0003g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1202+1094C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794101 | |||||||
| chr12:124794127 | T | A | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1202+1068A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794127 | |||||||
| chr12:124794135 | G | A | 1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1202+1060C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794135 | |||||||
| chr12:124794196 | T | C | 4 | a0001c0001t0017g0030 a0001c0001t0019g0061 a0001c0004t0011g0119 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202+999A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794196 | |||||||
| chr12:124794245 | G | A | 97 | a0001c0001t0001g0301 a0001c0001t0001g0318 a0001c0001t0002g0065 others(94): Show |
97 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1202+950C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794245 | |||||||
| chr12:124794272 | A | AG | 15 | a0001c0004t0001g0099 a0001c0004t0001g0102 a0001c0004t0001g0154 others(12): Show |
15 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1202+922dupC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794272 | |||||||
| chr12:124794400 | C | CT | 76 | a0001c0001t0001g0050 a0001c0001t0001g0067 a0001c0001t0001g0080 others(73): Show |
76 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1202+794dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794400 | |||||||
| chr12:124794400 | C | CTTTTTT | 9 | a0001c0001t0001g0040 a0001c0001t0005g0045 a0001c0001t0005g0243 others(6): Show |
9 | HG01884.hp2 HG01943.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1202+789_1202+794d others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794400 | |||||||
| chr12:124794400 | C | CTTTTTTT | 79 | a0001c0001t0001g0111 a0001c0001t0001g0301 a0001c0001t0001g0318 others(76): Show |
79 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1202+788_1202+794d others(9): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794400 | |||||||
| chr12:124794400 | C | CTTTTTTT others(1): Show |
20 | a0001c0001t0002g0221 a0001c0001t0003g0038 a0001c0001t0003g0169 others(17): Show |
20 | HG00438.hp1 HG00621.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1202+787_1202+794d others(10): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794400 | |||||||
| chr12:124794652 | C | T | 67 | a0001c0001t0001g0301 a0001c0001t0001g0318 a0001c0001t0002g0065 others(64): Show |
67 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.1202+543G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794652 | |||||||
| chr12:124794682 | G | A | 4 | a0001c0001t0003g0038 a0001c0001t0003g0224 a0001c0001t0008g0027 others(1): Show |
4 | HG01361.hp1 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1202+513C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794682 | |||||||
| chr12:124794737 | C | G | 1 | a0001c0003t0002g0317 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1202+458G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794737 | |||||||
| chr12:124794845 | G | A | 3 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0016g0240 |
3 | HG01243.hp1 HG02258.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1202+350C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794845 | |||||||
| chr12:124794879 | A | G | 2 | a0001c0002t0003g0076 a0001c0002t0003g0077 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1202+316T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794879 | |||||||
| chr12:124794886 | C | T | 25 | a0001c0001t0002g0128 a0001c0001t0003g0161 a0001c0001t0003g0165 others(22): Show |
25 | HG01243.hp2 HG01256.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1202+309G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794886 | |||||||
| chr12:124794978 | TG | T | 99 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0301 others(96): Show |
99 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1202+216delC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124794978 | |||||||
| chr12:124795115 | C | T | 32 | a0001c0001t0001g0301 a0001c0001t0002g0234 a0001c0001t0002g0310 others(29): Show |
32 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1202+80G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124795115 | |||||||
| chr12:124795177 | C | T | 1 | a0001c0004t0001g0102 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1202+18G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 9/12 | chr12 | 124795177 | |||||||
| chr12:124795275 | C | T | 18 | a0001c0001t0003g0161 a0001c0001t0003g0165 a0001c0001t0003g0226 others(15): Show |
18 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.1129-7G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124795275 | |||||||
| chr12:124795362 | C | T | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1129-94G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124795362 | |||||||
| chr12:124795363 | G | A | 1 | a0001c0003t0002g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1129-95C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124795363 | |||||||
| chr12:124795421 | TG | T | 99 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0301 others(96): Show |
99 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1129-154delC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124795421 | |||||||
| chr12:124795429 | G | T | 6 | a0001c0001t0005g0045 a0001c0001t0008g0036 a0001c0001t0008g0037 others(3): Show |
6 | HG01884.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1129-161C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124795429 | |||||||
| chr12:124795673 | A | G | 1 | a0001c0002t0001g0168 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1129-405T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124795673 | |||||||
| chr12:124795724 | T | C | 1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1129-456A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124795724 | |||||||
| chr12:124795886 | G | A | 68 | a0001c0001t0001g0301 a0001c0001t0001g0318 a0001c0001t0002g0065 others(65): Show |
68 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1129-618C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124795886 | |||||||
| chr12:124795961 | T | C | 110 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0301 others(107): Show |
110 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1129-693A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124795961 | |||||||
| chr12:124796177 | C | G | 14 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0038 others(11): Show |
14 | HG01081.hp2 HG01123.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1129-909G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124796177 | |||||||
| chr12:124796199 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1129-931G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124796199 | |||||||
| chr12:124796231 | G | A | 11 | a0001c0004t0001g0099 a0001c0004t0001g0102 a0001c0004t0001g0154 others(8): Show |
11 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.1129-963C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124796231 | |||||||
| chr12:124796265 | A | G | 1 | a0001c0002t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1129-997T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124796265 | |||||||
| chr12:124796349 | C | T | 68 | a0001c0001t0001g0301 a0001c0001t0001g0318 a0001c0001t0002g0065 others(65): Show |
68 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1129-1081G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124796349 | |||||||
| chr12:124796403 | C | CT | 19 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0117 others(16): Show |
19 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.1129-1136dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124796403 | |||||||
| chr12:124796491 | T | C | 3 | a0001c0001t0017g0030 a0001c0004t0011g0119 a0002c0006t0004g0012 |
3 | HG02055.hp2 HG02109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1129-1223A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124796491 | |||||||
| chr12:124796515 | G | A | 25 | a0001c0001t0002g0128 a0001c0001t0003g0161 a0001c0001t0003g0165 others(22): Show |
25 | HG01243.hp2 HG01256.hp2 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1129-1247C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124796515 | |||||||
| chr12:124796534 | G | A | 6 | a0001c0001t0005g0045 a0001c0001t0008g0036 a0001c0001t0008g0037 others(3): Show |
6 | HG01884.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1129-1266C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124796534 | |||||||
| chr12:124796556 | G | T | 135 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0001g0301 others(132): Show |
135 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1129-1288C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124796556 | |||||||
| chr12:124796851 | C | T | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1129-1583G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124796851 | |||||||
| chr12:124797128 | T | C | 1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1129-1860A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124797128 | |||||||
| chr12:124797217 | C | T | 2 | a0001c0016t0001g0021 a0001c0017t0005g0341 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1129-1949G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124797217 | |||||||
| chr12:124797274 | C | T | 97 | a0001c0001t0001g0301 a0001c0001t0001g0318 a0001c0001t0002g0065 others(94): Show |
97 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1129-2006G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124797274 | |||||||
| chr12:124797309 | G | A | 2 | a0001c0016t0001g0021 a0001c0017t0005g0341 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1129-2041C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124797309 | |||||||
| chr12:124797503 | C | T | 1 | a0002c0008t0001g0005 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1129-2235G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124797503 | |||||||
| chr12:124797535 | C | T | 77 | a0001c0001t0001g0301 a0001c0001t0001g0318 a0001c0001t0002g0065 others(74): Show |
77 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1129-2267G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124797535 | |||||||
| chr12:124797653 | C | T | 79 | a0001c0001t0001g0067 a0001c0001t0001g0301 a0001c0001t0001g0318 others(76): Show |
79 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1129-2385G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124797653 | |||||||
| chr12:124797660 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1129-2392A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124797660 | |||||||
| chr12:124797700 | G | A | 3 | a0001c0001t0003g0086 a0001c0001t0003g0087 a0001c0001t0003g0089 |
3 | HG00280.hp2 HG00323.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1128+2424C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124797700 | |||||||
| chr12:124798023 | C | T | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1128+2101G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798023 | |||||||
| chr12:124798142 | G | A | 14 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0016g0240 others(11): Show |
14 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.1128+1982C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798142 | |||||||
| chr12:124798148 | C | T | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1128+1976G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798148 | |||||||
| chr12:124798160 | C | G | 1 | a0001c0001t0003g0232 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1128+1964G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798160 | |||||||
| chr12:124798336 | A | G | 261 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(258): Show |
261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.1128+1788T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798336 | |||||||
| chr12:124798415 | A | C | 94 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(91): Show |
94 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1128+1709T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798415 | |||||||
| chr12:124798425 | T | A | 2 | a0001c0002t0001g0205 a0001c0007t0001g0090 |
2 | HG02602.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1128+1699A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798425 | |||||||
| chr12:124798557 | T | G | 2 | a0001c0002t0001g0220 a0001c0002t0001g0311 |
2 | NA18944.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1128+1567A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798557 | |||||||
| chr12:124798608 | C | T | 32 | a0001c0001t0002g0128 a0001c0001t0003g0232 a0001c0001t0004g0026 others(29): Show |
32 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.1128+1516G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798608 | |||||||
| chr12:124798609 | G | A | 1 | a0001c0007t0003g0135 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1128+1515C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798609 | |||||||
| chr12:124798613 | C | T | 1 | a0001c0002t0005g0255 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1128+1511G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798613 | |||||||
| chr12:124798650 | A | G | 261 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(258): Show |
261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.1128+1474T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798650 | |||||||
| chr12:124798668 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0184 |
2 | HG01975.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1128+1456G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798668 | |||||||
| chr12:124798685 | A | C | 10 | a0001c0002t0001g0158 a0001c0002t0001g0205 a0001c0002t0003g0075 others(7): Show |
10 | HG01069.hp2 HG01256.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.1128+1439T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798685 | |||||||
| chr12:124798811 | T | C | 2 | a0001c0003t0002g0095 a0001c0003t0002g0192 |
2 | NA18939.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1128+1313A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798811 | |||||||
| chr12:124798828 | G | A | 1 | a0001c0002t0009g0055 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1128+1296C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798828 | |||||||
| chr12:124798846 | G | GA | 92 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0145 others(89): Show |
92 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1128+1277dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798846 | |||||||
| chr12:124798851 | A | T | 1 | a0001c0001t0003g0114 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1128+1273T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798851 | |||||||
| chr12:124798857 | G | A | 261 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(258): Show |
261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.1128+1267C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798857 | |||||||
| chr12:124798975 | C | T | 94 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(91): Show |
94 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1128+1149G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124798975 | |||||||
| chr12:124799051 | A | G | 1 | a0001c0001t0017g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1128+1073T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124799051 | |||||||
| chr12:124799175 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0228 |
2 | HG02040.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1128+949G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124799175 | |||||||
| chr12:124799189 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1128+935C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124799189 | |||||||
| chr12:124799220 | C | T | 262 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(259): Show |
262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.1128+904G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124799220 | |||||||
| chr12:124799305 | G | A | 1 | a0001c0003t0002g0182 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1128+819C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124799305 | |||||||
| chr12:124799308 | T | G | 1 | a0001c0001t0019g0061 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1128+816A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124799308 | |||||||
| chr12:124799345 | C | T | 149 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0111 others(146): Show |
149 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.1128+779G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124799345 | |||||||
| chr12:124799388 | G | A | 5 | a0001c0001t0003g0038 a0001c0001t0003g0170 a0001c0001t0003g0224 others(2): Show |
5 | HG01361.hp1 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1128+736C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124799388 | |||||||
| chr12:124799509 | C | T | 10 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0117 others(7): Show |
10 | HG01081.hp2 HG01123.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.1128+615G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124799509 | |||||||
| chr12:124799822 | C | T | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1128+302G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124799822 | |||||||
| chr12:124800051 | G | T | 14 | a0001c0001t0001g0223 a0001c0001t0003g0023 a0001c0001t0003g0029 others(11): Show |
14 | HG01884.hp2 HG02257.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1128+73C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 8/12 | chr12 | 124800051 | |||||||
| chr12:124800627 | C | T | 3 | a0001c0001t0003g0086 a0001c0001t0003g0087 a0001c0001t0003g0089 |
3 | HG00280.hp2 HG00323.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1010-385G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124800627 | |||||||
| chr12:124800628 | G | A | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1010-386C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124800628 | |||||||
| chr12:124800826 | A | C | 3 | a0001c0001t0003g0086 a0001c0001t0003g0087 a0001c0001t0003g0089 |
3 | HG00280.hp2 HG00323.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1010-584T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124800826 | |||||||
| chr12:124800851 | C | T | 1 | a0001c0001t0017g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1010-609G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124800851 | |||||||
| chr12:124800901 | C | T | 1 | a0001c0007t0003g0135 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1010-659G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124800901 | |||||||
| chr12:124801071 | T | G | 1 | a0001c0002t0003g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1010-829A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801071 | |||||||
| chr12:124801114 | G | A | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1010-872C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801114 | |||||||
| chr12:124801159 | A | T | 32 | a0001c0001t0002g0128 a0001c0001t0003g0232 a0001c0001t0004g0026 others(29): Show |
32 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.1010-917T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801159 | |||||||
| chr12:124801188 | G | A | 1 | a0001c0001t0004g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1010-946C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801188 | |||||||
| chr12:124801407 | T | C | 259 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(256): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1010-1165A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801407 | |||||||
| chr12:124801491 | T | C | 259 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(256): Show |
259 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1010-1249A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801491 | |||||||
| chr12:124801678 | GC | G | 4 | a0001c0001t0002g0128 a0001c0001t0005g0084 a0002c0006t0002g0017 others(1): Show |
4 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1010-1437delG | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801678 | |||||||
| chr12:124801702 | C | G | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1010-1460G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801702 | |||||||
| chr12:124801708 | C | A | 108 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(105): Show |
108 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1010-1466G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801708 | |||||||
| chr12:124801721 | G | A | 1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1010-1479C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801721 | |||||||
| chr12:124801770 | T | C | 12 | a0001c0004t0001g0099 a0001c0004t0001g0102 a0001c0004t0001g0154 others(9): Show |
12 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1010-1528A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801770 | |||||||
| chr12:124801796 | A | G | 3 | a0001c0004t0001g0099 a0001c0004t0002g0271 a0001c0004t0004g0195 |
3 | NA18965.hp1 NA18983.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1010-1554T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801796 | |||||||
| chr12:124801962 | C | T | 1 | a0001c0002t0003g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1010-1720G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801962 | |||||||
| chr12:124801988 | T | C | 1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1010-1746A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124801988 | |||||||
| chr12:124802104 | T | C | 108 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(105): Show |
108 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1010-1862A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802104 | |||||||
| chr12:124802149 | C | CA | 53 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0145 others(50): Show |
53 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.1010-1908dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802149 | |||||||
| chr12:124802149 | C | CAA | 23 | a0001c0001t0001g0080 a0001c0001t0001g0152 a0001c0001t0003g0161 others(20): Show |
23 | HG00323.hp2 HG00639.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1010-1909_1010-190 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802149 | |||||||
| chr12:124802149 | C | CAAA | 82 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(79): Show |
82 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1010-1910_1010-190 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802149 | |||||||
| chr12:124802149 | CA | C | 9 | a0001c0001t0011g0235 a0001c0002t0001g0177 a0001c0002t0002g0320 others(6): Show |
9 | HG00639.hp2 HG01256.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1010-1908delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802149 | |||||||
| chr12:124802182 | A | G | 90 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(87): Show |
90 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1010-1940T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802182 | |||||||
| chr12:124802359 | A | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0038 others(12): Show |
15 | HG01081.hp2 HG01123.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1010-2117T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802359 | |||||||
| chr12:124802427 | C | G | 2 | a0001c0004t0015g0044 a0001c0004t0015g0059 |
2 | HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1010-2185G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802427 | |||||||
| chr12:124802533 | C | T | 12 | a0001c0001t0004g0026 a0001c0001t0004g0042 a0001c0001t0004g0124 others(9): Show |
12 | HG01109.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1010-2291G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802533 | |||||||
| chr12:124802565 | G | A | 148 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0111 others(145): Show |
148 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1010-2323C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802565 | |||||||
| chr12:124802620 | C | T | 1 | a0001c0002t0001g0158 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1010-2378G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802620 | |||||||
| chr12:124802670 | A | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(88): Show |
91 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1010-2428T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802670 | |||||||
| chr12:124802834 | C | A | 34 | a0001c0001t0001g0223 a0001c0001t0003g0023 a0001c0001t0003g0029 others(31): Show |
34 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1010-2592G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802834 | |||||||
| chr12:124802992 | A | C | 15 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0003g0038 others(12): Show |
15 | HG01081.hp2 HG01123.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.1010-2750T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802992 | |||||||
| chr12:124802995 | A | T | 1 | a0001c0003t0001g0098 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1010-2753T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124802995 | |||||||
| chr12:124803036 | G | C | 1 | a0001c0002t0001g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1010-2794C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803036 | |||||||
| chr12:124803081 | A | G | 1 | a0001c0002t0003g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1010-2839T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803081 | |||||||
| chr12:124803099 | C | G | 2 | a0001c0002t0002g0073 a0001c0002t0002g0088 |
2 | HG01070.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1010-2857G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803099 | |||||||
| chr12:124803100 | G | A | 2 | a0001c0004t0011g0119 a0001c0004t0014g0190 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1010-2858C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803100 | |||||||
| chr12:124803102 | A | G | 150 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(147): Show |
150 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.1010-2860T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803102 | |||||||
| chr12:124803399 | G | A | 2 | a0001c0004t0011g0119 a0001c0004t0014g0190 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1010-3157C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803399 | |||||||
| chr12:124803487 | A | G | 1 | a0001c0001t0003g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1010-3245T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803487 | |||||||
| chr12:124803513 | T | A | 1 | a0001c0001t0005g0243 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1010-3271A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803513 | |||||||
| chr12:124803562 | T | C | 131 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0111 others(128): Show |
131 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1010-3320A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803562 | |||||||
| chr12:124803689 | C | CA | 30 | a0001c0001t0003g0161 a0001c0001t0003g0165 a0001c0001t0003g0226 others(27): Show |
30 | HG00621.hp1 HG01106.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1010-3448dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803689 | |||||||
| chr12:124803689 | CA | C | 22 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0004g0026 others(19): Show |
22 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.1010-3448delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803689 | |||||||
| chr12:124803689 | CAAA | C | 18 | a0001c0001t0001g0040 a0001c0001t0001g0111 a0001c0001t0002g0065 others(15): Show |
18 | HG01081.hp2 HG01123.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.1010-3450_1010-344 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803689 | |||||||
| chr12:124803689 | CAAAA | C | 75 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0145 others(72): Show |
75 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1010-3451_1010-344 others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803689 | |||||||
| chr12:124803689 | CAAAAA | C | 6 | a0001c0003t0002g0069 a0001c0003t0002g0268 a0001c0003t0002g0275 others(3): Show |
6 | HG02109.hp2 HG03453.hp1 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.1010-3452_1010-344 others(9): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803689 | |||||||
| chr12:124803689 | CAAAAAAA others(2): Show |
C | 10 | a0001c0004t0001g0099 a0001c0004t0001g0154 a0001c0004t0001g0293 others(7): Show |
10 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.1010-3456_1010-344 others(13): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803689 | |||||||
| chr12:124803689 | CAAAAAAA others(6): Show |
C | 16 | a0001c0001t0001g0223 a0001c0001t0003g0023 a0001c0001t0003g0029 others(13): Show |
16 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1010-3460_1010-344 others(17): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803689 | |||||||
| chr12:124803714 | AAT | A | 80 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0067 others(77): Show |
80 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1010-3474_1010-347 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803714 | |||||||
| chr12:124803715 | AT | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0003g0020 others(4): Show |
7 | HG01109.hp2 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1010-3474delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803715 | |||||||
| chr12:124803716 | T | A | 2 | a0001c0001t0004g0297 a0001c0001t0012g0062 |
2 | HG02135.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1010-3474A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803716 | |||||||
| chr12:124803725 | GATAAA | G | 11 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(8): Show |
11 | HG01175.hp1 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1010-3488_1010-348 others(9): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803725 | |||||||
| chr12:124803922 | A | G | 2 | a0001c0001t0008g0027 a0001c0001t0008g0125 |
2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1010-3680T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803922 | |||||||
| chr12:124803942 | G | A | 12 | a0001c0004t0001g0099 a0001c0004t0001g0102 a0001c0004t0001g0154 others(9): Show |
12 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1010-3700C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803942 | |||||||
| chr12:124803982 | C | T | 1 | a0001c0005t0004g0347 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1010-3740G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803982 | |||||||
| chr12:124803983 | G | A | 1 | a0001c0001t0017g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1010-3741C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124803983 | |||||||
| chr12:124804002 | G | A | 1 | a0001c0001t0008g0046 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1009+3759C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804002 | |||||||
| chr12:124804031 | T | C | 4 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0016g0240 others(1): Show |
4 | HG01243.hp1 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009+3730A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804031 | |||||||
| chr12:124804032 | C | T | 4 | a0001c0001t0002g0128 a0001c0001t0005g0084 a0002c0006t0002g0017 others(1): Show |
4 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009+3729G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804032 | |||||||
| chr12:124804058 | C | T | 150 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0111 others(147): Show |
150 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.1009+3703G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804058 | |||||||
| chr12:124804115 | G | C | 90 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(87): Show |
90 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1009+3646C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804115 | |||||||
| chr12:124804121 | T | G | 90 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(87): Show |
90 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1009+3640A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804121 | |||||||
| chr12:124804139 | G | A | 17 | a0001c0001t0003g0161 a0001c0001t0003g0165 a0001c0001t0003g0226 others(14): Show |
17 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1009+3622C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804139 | |||||||
| chr12:124804177 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1009+3584A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804177 | |||||||
| chr12:124804195 | T | A | 1 | a0001c0005t0004g0353 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1009+3566A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804195 | |||||||
| chr12:124804236 | T | C | 4 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0016g0240 others(1): Show |
4 | HG01243.hp1 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1009+3525A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804236 | |||||||
| chr12:124804259 | T | TG | 3 | a0001c0004t0001g0181 a0001c0004t0001g0293 a0001c0004t0002g0238 |
3 | HG00673.hp2 HG02056.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1009+3501dupC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804259 | |||||||
| chr12:124804344 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1009+3417C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804344 | |||||||
| chr12:124804517 | C | T | 1 | a0001c0002t0003g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1009+3244G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804517 | |||||||
| chr12:124804518 | G | A | 7 | a0001c0001t0002g0128 a0001c0001t0005g0084 a0001c0016t0001g0021 others(4): Show |
7 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009+3243C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804518 | |||||||
| chr12:124804544 | G | T | 7 | a0001c0001t0002g0128 a0001c0001t0005g0084 a0001c0016t0001g0021 others(4): Show |
7 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009+3217C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804544 | |||||||
| chr12:124804638 | G | A | 3 | a0001c0001t0002g0292 a0001c0001t0002g0316 a0001c0001t0002g0335 |
3 | NA18970.hp1 NA19001.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1009+3123C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804638 | |||||||
| chr12:124804693 | G | A | 7 | a0001c0001t0002g0128 a0001c0001t0005g0084 a0001c0016t0001g0021 others(4): Show |
7 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009+3068C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804693 | |||||||
| chr12:124804719 | G | A | 90 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(87): Show |
90 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.1009+3042C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804719 | |||||||
| chr12:124804805 | G | A | 19 | a0001c0001t0003g0161 a0001c0001t0003g0165 a0001c0001t0003g0226 others(16): Show |
19 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1009+2956C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124804805 | |||||||
| chr12:124805106 | CACCAAGA others(21): Show |
C | 127 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0111 others(124): Show |
127 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1009+2627_1009+265 others(32): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805106 | |||||||
| chr12:124805122 | G | A | 6 | a0001c0001t0002g0253 a0001c0001t0003g0294 a0001c0001t0004g0297 others(3): Show |
6 | HG02015.hp2 HG02083.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1009+2639C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805122 | |||||||
| chr12:124805129 | A | G | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1009+2632T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805129 | |||||||
| chr12:124805137 | C | CTAGCTCT others(1267): Show |
1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1009+2623_1009+262 others(1278): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805137 | |||||||
| chr12:124805140 | G | A | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1009+2621C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805140 | |||||||
| chr12:124805142 | C | A | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1009+2619G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805142 | |||||||
| chr12:124805145 | G | A | 1 | a0001c0001t0017g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1009+2616C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805145 | |||||||
| chr12:124805439 | T | C | 155 | a0001c0001t0001g0040 a0001c0001t0001g0072 a0001c0001t0001g0111 others(152): Show |
155 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1009+2322A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805439 | |||||||
| chr12:124805440 | G | C | 1 | a0001c0003t0002g0069 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1009+2321C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805440 | |||||||
| chr12:124805490 | A | G | 85 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0067 others(82): Show |
85 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1009+2271T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805490 | |||||||
| chr12:124805525 | G | A | 1 | a0001c0003t0002g0231 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1009+2236C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805525 | |||||||
| chr12:124805704 | A | G | 3 | a0001c0002t0001g0178 a0001c0002t0001g0217 a0001c0002t0024g0265 |
3 | HG02683.hp2 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1009+2057T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805704 | |||||||
| chr12:124805725 | A | AT | 86 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0067 others(83): Show |
86 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1009+2035dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805725 | |||||||
| chr12:124805725 | A | ATT | 16 | a0001c0001t0001g0039 a0001c0001t0001g0144 a0001c0001t0001g0146 others(13): Show |
16 | HG01175.hp1 HG01175.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1009+2034_1009+203 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805725 | |||||||
| chr12:124805725 | A | ATTT | 22 | a0001c0001t0001g0132 a0001c0001t0001g0272 a0001c0001t0002g0128 others(19): Show |
22 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.1009+2033_1009+203 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805725 | |||||||
| chr12:124805725 | A | ATTTT | 7 | a0001c0001t0017g0030 a0001c0002t0007g0201 a0001c0004t0001g0102 others(4): Show |
7 | HG01433.hp1 HG02056.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009+2032_1009+203 others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805725 | |||||||
| chr12:124805725 | AT | A | 6 | a0001c0001t0001g0052 a0001c0002t0001g0141 a0001c0002t0001g0282 others(3): Show |
6 | HG01070.hp2 HG02602.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.1009+2035delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805725 | |||||||
| chr12:124805725 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0002g0229 a0001c0002t0001g0306 |
2 | HG02027.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1009+2025_1009+203 others(15): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805725 | |||||||
| chr12:124805746 | TTTTG | T | 91 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0145 others(88): Show |
91 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1009+2011_1009+201 others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805746 | |||||||
| chr12:124805747 | TTTG | T | 17 | a0001c0001t0001g0223 a0001c0001t0003g0029 a0001c0001t0003g0183 others(14): Show |
17 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1009+2011_1009+201 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805747 | |||||||
| chr12:124805748 | TTG | T | 15 | a0001c0001t0003g0023 a0001c0001t0003g0169 a0001c0001t0003g0237 others(12): Show |
15 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1009+2011_1009+201 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805748 | |||||||
| chr12:124805750 | G | T | 27 | a0001c0001t0002g0128 a0001c0001t0005g0084 a0001c0001t0017g0030 others(24): Show |
27 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.1009+2011C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805750 | |||||||
| chr12:124805812 | C | T | 1 | a0001c0001t0018g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1009+1949G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805812 | |||||||
| chr12:124805822 | G | A | 1 | a0002c0006t0003g0008 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1009+1939C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805822 | |||||||
| chr12:124805865 | C | T | 1 | a0001c0002t0003g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1009+1896G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805865 | |||||||
| chr12:124805891 | C | G | 153 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0145 others(150): Show |
153 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1009+1870G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124805891 | |||||||
| chr12:124806007 | G | A | 19 | a0001c0001t0003g0161 a0001c0001t0003g0165 a0001c0001t0003g0226 others(16): Show |
19 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1009+1754C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806007 | |||||||
| chr12:124806151 | T | C | 1 | a0001c0001t0017g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1009+1610A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806151 | |||||||
| chr12:124806177 | C | T | 1 | a0001c0003t0001g0098 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1009+1584G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806177 | |||||||
| chr12:124806184 | G | A | 2 | a0001c0004t0011g0119 a0001c0004t0014g0190 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1009+1577C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806184 | |||||||
| chr12:124806206 | G | T | 1 | a0001c0001t0017g0030 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1009+1555C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806206 | |||||||
| chr12:124806228 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0146 a0001c0001t0001g0162 others(4): Show |
7 | HG01175.hp1 HG02257.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009+1533C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806228 | |||||||
| chr12:124806228 | G | C | 1 | a0001c0007t0010g0156 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1009+1533C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806228 | |||||||
| chr12:124806277 | G | A | 1 | a0001c0004t0011g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1009+1484C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806277 | |||||||
| chr12:124806310 | A | T | 243 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(240): Show |
243 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.1009+1451T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806310 | |||||||
| chr12:124806319 | C | T | 13 | a0001c0004t0001g0099 a0001c0004t0001g0102 a0001c0004t0001g0154 others(10): Show |
13 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1009+1442G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806319 | |||||||
| chr12:124806444 | A | C | 12 | a0001c0001t0003g0038 a0001c0001t0003g0117 a0001c0001t0003g0170 others(9): Show |
12 | HG01123.hp2 HG01361.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1009+1317T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806444 | |||||||
| chr12:124806460 | A | G | 153 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0145 others(150): Show |
153 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.1009+1301T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806460 | |||||||
| chr12:124806571 | C | T | 1 | a0003c0019t0011g0342 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1009+1190G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806571 | |||||||
| chr12:124806577 | G | T | 1 | a0002c0006t0006g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1009+1184C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806577 | |||||||
| chr12:124806691 | T | C | 27 | a0001c0001t0001g0223 a0001c0001t0003g0023 a0001c0001t0003g0029 others(24): Show |
27 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1009+1070A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806691 | |||||||
| chr12:124806781 | G | A | 3 | a0001c0002t0001g0327 a0001c0004t0011g0119 a0001c0004t0014g0190 |
3 | HG02055.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1009+980C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806781 | |||||||
| chr12:124806917 | G | A | 13 | a0001c0004t0001g0099 a0001c0004t0001g0102 a0001c0004t0001g0154 others(10): Show |
13 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1009+844C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806917 | |||||||
| chr12:124806924 | C | T | 1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1009+837G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124806924 | |||||||
| chr12:124807001 | C | T | 1 | a0001c0003t0004g0321 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1009+760G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124807001 | |||||||
| chr12:124807094 | G | A | 13 | a0001c0004t0001g0099 a0001c0004t0001g0102 a0001c0004t0001g0154 others(10): Show |
13 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1009+667C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124807094 | |||||||
| chr12:124807132 | C | T | 13 | a0001c0004t0001g0099 a0001c0004t0001g0102 a0001c0004t0001g0154 others(10): Show |
13 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1009+629G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124807132 | |||||||
| chr12:124807209 | T | A | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1009+552A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124807209 | |||||||
| chr12:124807260 | T | C | 13 | a0001c0004t0001g0099 a0001c0004t0001g0102 a0001c0004t0001g0154 others(10): Show |
13 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1009+501A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124807260 | |||||||
| chr12:124807333 | T | G | 1 | a0001c0003t0002g0315 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1009+428A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124807333 | |||||||
| chr12:124807382 | C | T | 123 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0145 others(120): Show |
123 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.1009+379G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124807382 | |||||||
| chr12:124807431 | G | A | 12 | a0001c0004t0001g0099 a0001c0004t0001g0102 a0001c0004t0001g0154 others(9): Show |
12 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1009+330C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124807431 | |||||||
| chr12:124807466 | C | T | 93 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0145 others(90): Show |
93 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1009+295G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124807466 | |||||||
| chr12:124807622 | C | T | 1 | a0001c0001t0005g0243 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1009+139G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124807622 | |||||||
| chr12:124807638 | G | A | 2 | a0001c0016t0001g0021 a0001c0017t0005g0341 |
2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1009+123C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 7/12 | chr12 | 124807638 | |||||||
| chr12:124807970 | C | T | 2 | a0002c0006t0004g0012 a0002c0006t0006g0011 |
2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.843-43G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124807970 | |||||||
| chr12:124808107 | C | T | 9 | a0001c0001t0002g0128 a0001c0001t0005g0084 a0001c0002t0001g0332 others(6): Show |
9 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.843-180G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124808107 | |||||||
| chr12:124808129 | T | C | 141 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0145 others(138): Show |
141 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.843-202A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124808129 | |||||||
| chr12:124808161 | A | G | 3 | a0001c0004t0011g0119 a0001c0004t0014g0190 a0002c0006t0004g0012 |
3 | HG02055.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.843-234T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124808161 | |||||||
| chr12:124808338 | A | C | 29 | a0001c0001t0001g0223 a0001c0001t0003g0023 a0001c0001t0003g0029 others(26): Show |
29 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.843-411T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124808338 | |||||||
| chr12:124808557 | C | T | 5 | a0001c0001t0003g0038 a0001c0001t0003g0170 a0001c0001t0003g0224 others(2): Show |
5 | HG01361.hp1 HG01891.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.843-630G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124808557 | |||||||
| chr12:124808621 | G | A | 4 | a0001c0001t0002g0229 a0001c0001t0003g0267 a0001c0002t0001g0282 others(1): Show |
4 | HG02027.hp1 HG02155.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.843-694C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124808621 | |||||||
| chr12:124808625 | C | T | 2 | a0001c0002t0001g0252 a0001c0002t0001g0304 |
2 | HG02027.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.843-698G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124808625 | |||||||
| chr12:124808714 | A | G | 1 | a0001c0004t0003g0203 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.843-787T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124808714 | |||||||
| chr12:124808730 | C | G | 1 | a0001c0002t0001g0306 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.843-803G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124808730 | |||||||
| chr12:124808839 | CA | C | 47 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0186 others(44): Show |
47 | HG00621.hp1 HG01069.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.843-913delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124808839 | |||||||
| chr12:124808948 | T | C | 1 | a0001c0003t0002g0066 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.843-1021A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124808948 | |||||||
| chr12:124809011 | G | A | 40 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0186 others(37): Show |
40 | HG00621.hp1 HG01069.hp2 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.843-1084C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809011 | |||||||
| chr12:124809051 | T | C | 174 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0072 others(171): Show |
174 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(171): Show |
intron_variant | MODIFIER | c.842+1123A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809051 | |||||||
| chr12:124809069 | A | G | 27 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0186 others(24): Show |
27 | HG00621.hp1 HG01069.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.842+1105T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809069 | |||||||
| chr12:124809073 | T | C | 83 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(80): Show |
83 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.842+1101A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809073 | |||||||
| chr12:124809140 | A | G | 88 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.842+1034T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809140 | |||||||
| chr12:124809197 | G | A | 1 | a0001c0003t0001g0098 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.842+977C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809197 | |||||||
| chr12:124809349 | C | T | 28 | a0001c0001t0001g0223 a0001c0001t0003g0023 a0001c0001t0003g0029 others(25): Show |
28 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.842+825G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809349 | |||||||
| chr12:124809603 | C | G | 1 | a0001c0001t0004g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.842+571G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809603 | |||||||
| chr12:124809603 | C | T | 1 | a0001c0002t0001g0158 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.842+571G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809603 | |||||||
| chr12:124809704 | C | T | 1 | a0001c0002t0001g0049 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.842+470G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809704 | |||||||
| chr12:124809843 | A | G | 1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.842+331T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809843 | |||||||
| chr12:124809873 | G | T | 12 | a0001c0001t0003g0267 a0001c0004t0001g0099 a0001c0004t0001g0102 others(9): Show |
12 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.842+301C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809873 | |||||||
| chr12:124809895 | A | G | 1 | a0001c0001t0025g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.842+279T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809895 | |||||||
| chr12:124809979 | T | A | 13 | a0001c0001t0001g0112 a0001c0001t0001g0199 a0001c0001t0002g0253 others(10): Show |
13 | HG02015.hp1 HG02015.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.842+195A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 6/12 | chr12 | 124809979 | |||||||
| chr12:124810347 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.727-58G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810347 | |||||||
| chr12:124810388 | G | A | 1 | a0001c0004t0004g0195 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.727-99C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810388 | |||||||
| chr12:124810482 | C | T | 21 | a0001c0001t0003g0038 a0001c0001t0003g0117 a0001c0001t0003g0170 others(18): Show |
21 | HG00621.hp1 HG01123.hp2 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.727-193G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810482 | |||||||
| chr12:124810485 | G | A | 1 | a0001c0002t0001g0049 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.727-196C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810485 | |||||||
| chr12:124810498 | C | T | 1 | a0001c0003t0001g0098 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.727-209G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810498 | |||||||
| chr12:124810499 | G | A | 5 | a0001c0001t0005g0045 a0001c0001t0008g0046 a0001c0004t0015g0044 others(2): Show |
5 | HG02717.hp2 HG02896.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.727-210C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810499 | |||||||
| chr12:124810529 | T | C | 5 | a0001c0001t0005g0045 a0001c0001t0008g0046 a0001c0004t0015g0044 others(2): Show |
5 | HG02717.hp2 HG02896.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.727-240A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810529 | |||||||
| chr12:124810607 | C | T | 4 | a0001c0001t0002g0096 a0001c0002t0001g0141 a0001c0002t0001g0143 others(1): Show |
4 | NA18960.hp1 NA18990.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-318G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810607 | |||||||
| chr12:124810819 | G | C | 1 | a0001c0003t0004g0321 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.727-530C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810819 | |||||||
| chr12:124810837 | T | C | 143 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0052 others(140): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.727-548A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810837 | |||||||
| chr12:124810933 | G | T | 1 | a0001c0002t0021g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.727-644C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810933 | |||||||
| chr12:124810936 | G | A | 1 | a0001c0002t0003g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.727-647C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810936 | |||||||
| chr12:124810980 | C | T | 22 | a0001c0001t0002g0157 a0001c0001t0003g0038 a0001c0001t0003g0117 others(19): Show |
22 | HG00621.hp1 HG01123.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.727-691G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810980 | |||||||
| chr12:124810984 | G | C | 2 | a0001c0001t0007g0322 a0001c0001t0007g0323 |
2 | HG02015.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.727-695C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124810984 | |||||||
| chr12:124811073 | G | A | 1 | a0001c0005t0006g0344 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.727-784C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811073 | |||||||
| chr12:124811112 | G | A | 1 | a0001c0007t0001g0150 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.726+758C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811112 | |||||||
| chr12:124811129 | T | C | 246 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.726+741A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811129 | |||||||
| chr12:124811131 | T | C | 246 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.726+739A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811131 | |||||||
| chr12:124811184 | T | C | 248 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.726+686A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811184 | |||||||
| chr12:124811284 | T | G | 1 | a0001c0001t0002g0234 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.726+586A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811284 | |||||||
| chr12:124811315 | C | G | 1 | a0001c0001t0012g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.726+555G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811315 | |||||||
| chr12:124811335 | G | A | 29 | a0001c0001t0002g0157 a0001c0001t0003g0025 a0001c0001t0003g0038 others(26): Show |
29 | HG00621.hp1 HG01123.hp2 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.726+535C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811335 | |||||||
| chr12:124811368 | T | G | 11 | a0001c0001t0002g0128 a0001c0001t0005g0084 a0001c0002t0001g0332 others(8): Show |
11 | HG01256.hp2 HG01257.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.726+502A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811368 | |||||||
| chr12:124811448 | AT | A | 29 | a0001c0001t0002g0157 a0001c0001t0003g0025 a0001c0001t0003g0038 others(26): Show |
29 | HG00621.hp1 HG01123.hp2 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.726+421delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811448 | |||||||
| chr12:124811493 | G | A | 11 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.726+377C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811493 | |||||||
| chr12:124811520 | C | G | 3 | a0001c0002t0005g0336 a0001c0002t0005g0337 a0001c0002t0005g0338 |
3 | HG03491.hp1 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.726+350G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811520 | |||||||
| chr12:124811525 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.726+345G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811525 | |||||||
| chr12:124811534 | A | G | 56 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0105 others(53): Show |
57 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.726+336T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811534 | |||||||
| chr12:124811602 | G | A | 1 | a0002c0006t0004g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.726+268C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811602 | |||||||
| chr12:124811615 | C | T | 3 | a0001c0001t0008g0330 a0001c0001t0008g0331 a0001c0005t0020g0345 |
3 | HG02145.hp1 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.726+255G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811615 | |||||||
| chr12:124811815 | C | T | 6 | a0001c0001t0005g0045 a0001c0001t0008g0046 a0001c0004t0015g0044 others(3): Show |
6 | HG02717.hp2 HG02896.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.726+55G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811815 | |||||||
| chr12:124811816 | G | A | 3 | a0001c0001t0001g0144 a0002c0006t0001g0003 a0002c0006t0001g0004 |
3 | HG01109.hp2 HG01255.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.726+54C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811816 | |||||||
| chr12:124811840 | C | T | 1 | a0001c0002t0003g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.726+30G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 5/12 | chr12 | 124811840 | |||||||
| chr12:124812018 | G | A | 6 | a0001c0001t0005g0045 a0001c0001t0008g0046 a0001c0004t0015g0044 others(3): Show |
6 | HG02717.hp2 HG02896.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.631-53C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812018 | |||||||
| chr12:124812055 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.631-90G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812055 | |||||||
| chr12:124812158 | G | A | 2 | a0001c0017t0005g0341 a0002c0006t0006g0011 |
2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.631-193C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812158 | |||||||
| chr12:124812168 | G | A | 13 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0003g0260 others(10): Show |
13 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.631-203C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812168 | |||||||
| chr12:124812204 | G | A | 37 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0002g0128 others(34): Show |
37 | HG01243.hp2 HG01256.hp2 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.631-239C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812204 | |||||||
| chr12:124812326 | G | C | 1 | a0002c0006t0001g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.631-361C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812326 | |||||||
| chr12:124812364 | G | A | 78 | a0001c0001t0001g0034 a0001c0001t0003g0169 a0001c0001t0003g0237 others(75): Show |
78 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.631-399C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812364 | |||||||
| chr12:124812418 | C | T | 88 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0067 others(85): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.631-453G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812418 | |||||||
| chr12:124812454 | C | T | 2 | a0001c0017t0005g0341 a0002c0006t0006g0011 |
2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.631-489G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812454 | |||||||
| chr12:124812455 | G | A | 3 | a0001c0001t0001g0034 a0001c0016t0001g0021 a0003c0009t0003g0123 |
3 | HG02572.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.631-490C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812455 | |||||||
| chr12:124812775 | C | G | 27 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0161 others(24): Show |
27 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.631-810G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812775 | |||||||
| chr12:124812810 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.631-845T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812810 | |||||||
| chr12:124812843 | G | A | 1 | a0001c0003t0002g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.631-878C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812843 | |||||||
| chr12:124812878 | T | C | 225 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(222): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.631-913A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812878 | |||||||
| chr12:124812999 | A | C | 352 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(349): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.631-1034T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124812999 | |||||||
| chr12:124813023 | G | A | 1 | a0001c0001t0004g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.631-1058C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124813023 | |||||||
| chr12:124813080 | A | G | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.631-1115T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124813080 | |||||||
| chr12:124813086 | A | G | 342 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(339): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.630+1116T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124813086 | |||||||
| chr12:124813217 | C | T | 64 | a0001c0003t0001g0098 a0001c0003t0001g0106 a0001c0003t0001g0215 others(61): Show |
64 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.630+985G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124813217 | |||||||
| chr12:124813357 | A | C | 15 | a0001c0001t0003g0161 a0001c0001t0003g0226 a0001c0001t0004g0048 others(12): Show |
15 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.630+845T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124813357 | |||||||
| chr12:124813381 | A | G | 1 | a0004c0011t0002g0250 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.630+821T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124813381 | |||||||
| chr12:124813501 | A | G | 13 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0003g0260 others(10): Show |
13 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.630+701T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124813501 | |||||||
| chr12:124813632 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0004g0048 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.630+570G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124813632 | |||||||
| chr12:124813693 | A | C | 1 | a0006c0015t0001g0108 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.630+509T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124813693 | |||||||
| chr12:124813748 | T | C | 67 | a0001c0002t0001g0286 a0001c0003t0001g0098 a0001c0003t0001g0106 others(64): Show |
67 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.630+454A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124813748 | |||||||
| chr12:124813818 | C | T | 1 | a0001c0004t0002g0238 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.630+384G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124813818 | |||||||
| chr12:124814133 | G | GT | 4 | a0001c0001t0001g0132 a0001c0001t0001g0159 a0001c0001t0001g0228 others(1): Show |
4 | HG02040.hp2 NA18612.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+68dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124814133 | |||||||
| chr12:124814187 | C | T | 1 | a0001c0007t0001g0150 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.630+15G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 4/12 | chr12 | 124814187 | |||||||
| chr12:124814443 | G | A | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.427-38C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 3/12 | chr12 | 124814443 | |||||||
| chr12:124814470 | A | C | 1 | a0001c0007t0001g0063 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.427-65T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 3/12 | chr12 | 124814470 | |||||||
| chr12:124814485 | C | A | 2 | a0001c0001t0003g0232 a0001c0020t0003g0343 |
2 | HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.427-80G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 3/12 | chr12 | 124814485 | |||||||
| chr12:124814542 | G | A | 1 | a0001c0002t0003g0070 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.427-137C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 3/12 | chr12 | 124814542 | |||||||
| chr12:124814547 | T | C | 1 | a0001c0001t0025g0180 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.427-142A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 3/12 | chr12 | 124814547 | |||||||
| chr12:124814594 | T | C | 2 | a0001c0017t0005g0341 a0002c0006t0006g0011 |
2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.427-189A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 3/12 | chr12 | 124814594 | |||||||
| chr12:124814598 | C | T | 13 | a0001c0001t0002g0104 a0001c0001t0002g0221 a0001c0004t0001g0102 others(10): Show |
13 | HG00408.hp1 HG00438.hp1 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.427-193G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 3/12 | chr12 | 124814598 | |||||||
| chr12:124814823 | A | G | 94 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0105 others(91): Show |
95 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.426+150T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 3/12 | chr12 | 124814823 | |||||||
| chr12:124814856 | G | A | 4 | a0001c0001t0001g0132 a0001c0001t0001g0272 a0001c0001t0003g0232 others(1): Show |
4 | HG02572.hp2 NA19005.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.426+117C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 3/12 | chr12 | 124814856 | |||||||
| chr12:124814867 | C | T | 3 | a0001c0003t0002g0131 a0001c0003t0002g0317 a0001c0007t0003g0135 |
3 | HG00438.hp2 HG02040.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.426+106G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 3/12 | chr12 | 124814867 | |||||||
| chr12:124815131 | T | G | 2 | a0001c0001t0003g0142 a0001c0001t0003g0284 |
2 | HG02074.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.285-17A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124815131 | |||||||
| chr12:124815284 | C | T | 137 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.285-170G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124815284 | |||||||
| chr12:124815403 | AG | A | 24 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0003g0020 others(21): Show |
24 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.285-290delC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124815403 | |||||||
| chr12:124815437 | A | G | 333 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(330): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.285-323T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124815437 | |||||||
| chr12:124815495 | T | C | 23 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0003g0020 others(20): Show |
23 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.285-381A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124815495 | |||||||
| chr12:124815505 | G | C | 1 | a0001c0002t0003g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.285-391C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124815505 | |||||||
| chr12:124815530 | A | C | 1 | a0001c0003t0002g0069 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.285-416T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124815530 | |||||||
| chr12:124815593 | C | T | 1 | a0003c0009t0003g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.285-479G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124815593 | |||||||
| chr12:124815629 | G | T | 1 | a0001c0001t0001g0130 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.285-515C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124815629 | |||||||
| chr12:124815686 | C | T | 333 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(330): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.285-572G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124815686 | |||||||
| chr12:124815693 | A | C | 113 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0052 others(110): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.285-579T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124815693 | |||||||
| chr12:124815926 | G | T | 90 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0105 others(87): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.285-812C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124815926 | |||||||
| chr12:124816005 | G | A | 90 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0105 others(87): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.285-891C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816005 | |||||||
| chr12:124816029 | G | GT | 23 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0003g0020 others(20): Show |
23 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.285-916dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816029 | |||||||
| chr12:124816126 | T | G | 333 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(330): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.285-1012A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816126 | |||||||
| chr12:124816164 | C | T | 16 | a0001c0001t0002g0157 a0001c0001t0003g0025 a0001c0001t0003g0267 others(13): Show |
16 | HG00621.hp1 HG02055.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.285-1050G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816164 | |||||||
| chr12:124816180 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.285-1066G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816180 | |||||||
| chr12:124816238 | T | TTGTCCAC others(338): Show |
2 | a0001c0002t0001g0101 a0002c0006t0001g0002 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.285-1125_285-1124i others(347): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816238 | |||||||
| chr12:124816306 | G | A | 2 | a0003c0009t0003g0123 a0003c0019t0011g0342 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.285-1192C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816306 | |||||||
| chr12:124816428 | C | G | 4 | a0001c0001t0003g0117 a0001c0001t0003g0239 a0001c0001t0005g0043 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+1122G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816428 | |||||||
| chr12:124816491 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.284+1059A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816491 | |||||||
| chr12:124816668 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.284+882T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816668 | |||||||
| chr12:124816738 | G | A | 2 | a0001c0002t0001g0236 a0001c0002t0002g0320 |
2 | NA18948.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.284+812C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816738 | |||||||
| chr12:124816990 | T | TG | 17 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(14): Show |
17 | HG00099.hp2 HG00738.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.284+559dupC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816990 | |||||||
| chr12:124816998 | C | T | 3 | a0001c0001t0002g0253 a0001c0001t0007g0322 a0001c0001t0007g0323 |
3 | HG02015.hp2 HG02083.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.284+552G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124816998 | |||||||
| chr12:124817020 | A | ATG | 12 | a0001c0001t0001g0145 a0001c0001t0001g0272 a0001c0001t0006g0024 others(9): Show |
12 | HG01243.hp2 HG01433.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.284+528_284+529dup others(2): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817020 | |||||||
| chr12:124817020 | ATG | A | 79 | a0001c0001t0001g0130 a0001c0001t0003g0161 a0001c0001t0003g0226 others(76): Show |
79 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.284+528_284+529del others(2): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817020 | |||||||
| chr12:124817020 | ATGTG | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0094 a0001c0001t0018g0071 others(4): Show |
7 | HG01123.hp2 HG02647.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.284+526_284+529del others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817020 | |||||||
| chr12:124817020 | ATGTGTG | A | 98 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0105 others(95): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.284+524_284+529del others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817020 | |||||||
| chr12:124817020 | ATGTGTGT others(1): Show |
A | 6 | a0001c0001t0005g0045 a0001c0001t0008g0046 a0001c0004t0015g0044 others(3): Show |
6 | HG02717.hp2 HG02896.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+522_284+529del others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817020 | |||||||
| chr12:124817020 | ATGTGTGT others(9): Show |
A | 14 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0003g0260 others(11): Show |
14 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.284+514_284+529del others(16): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817020 | |||||||
| chr12:124817046 | GTGTATGT others(47): Show |
G | 1 | a0001c0002t0003g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.284+450_284+503del others(54): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817046 | |||||||
| chr12:124817050 | A | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0006g0041 others(4): Show |
7 | HG01884.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.284+500T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817050 | |||||||
| chr12:124817080 | GTGTA | G | 14 | a0001c0001t0003g0169 a0001c0001t0003g0237 a0001c0001t0003g0260 others(11): Show |
14 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.284+466_284+469del others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817080 | |||||||
| chr12:124817088 | ATG | A | 3 | a0001c0001t0003g0074 a0001c0001t0025g0180 a0001c0013t0016g0334 |
3 | HG01074.hp2 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.284+460_284+461del others(2): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817088 | |||||||
| chr12:124817112 | G | A | 1 | a0001c0007t0001g0107 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.284+438C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817112 | |||||||
| chr12:124817128 | GTGTGTA | G | 130 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.284+416_284+421del others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817128 | |||||||
| chr12:124817134 | A | ATGTATGT others(3): Show |
1 | a0001c0001t0011g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.284+415_284+416ins others(10): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817134 | |||||||
| chr12:124817134 | A | G | 2 | a0001c0017t0005g0341 a0002c0006t0006g0011 |
2 | HG02109.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.284+416T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817134 | |||||||
| chr12:124817274 | C | T | 1 | a0001c0001t0016g0240 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.284+276G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817274 | |||||||
| chr12:124817353 | T | TA | 89 | a0001c0001t0001g0034 a0001c0001t0001g0176 a0001c0001t0001g0184 others(86): Show |
89 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.284+196dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817353 | |||||||
| chr12:124817353 | T | TAA | 26 | a0001c0001t0001g0130 a0001c0001t0002g0305 a0001c0001t0003g0183 others(23): Show |
26 | HG00438.hp2 HG01934.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.284+195_284+196dup others(2): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817353 | |||||||
| chr12:124817353 | TA | T | 85 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0067 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.284+196delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817353 | |||||||
| chr12:124817353 | TAA | T | 41 | a0001c0001t0001g0039 a0001c0001t0001g0080 a0001c0001t0001g0092 others(38): Show |
41 | HG00323.hp2 HG00597.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.284+195_284+196del others(2): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817353 | |||||||
| chr12:124817374 | A | C | 4 | a0001c0001t0003g0232 a0001c0017t0005g0341 a0001c0020t0003g0343 others(1): Show |
4 | HG02109.hp2 HG02572.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+176T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817374 | |||||||
| chr12:124817482 | C | T | 5 | a0001c0001t0003g0023 a0001c0001t0003g0029 a0001c0001t0003g0183 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.284+68G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817482 | |||||||
| chr12:124817487 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.284+63G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 2/12 | chr12 | 124817487 | |||||||
| chr12:124817739 | G | A | 1 | a0001c0002t0003g0070 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.127-32C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124817739 | |||||||
| chr12:124817795 | C | T | 64 | a0001c0001t0001g0130 a0001c0001t0002g0305 a0001c0003t0001g0098 others(61): Show |
64 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.127-88G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124817795 | |||||||
| chr12:124817854 | C | T | 66 | a0001c0001t0001g0130 a0001c0001t0002g0305 a0001c0002t0002g0073 others(63): Show |
66 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.127-147G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124817854 | |||||||
| chr12:124817971 | G | A | 5 | a0001c0002t0001g0332 a0001c0002t0007g0058 a0001c0002t0007g0201 others(2): Show |
5 | HG01433.hp1 HG01928.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-264C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124817971 | |||||||
| chr12:124818007 | C | A | 66 | a0001c0001t0001g0130 a0001c0001t0002g0305 a0001c0002t0002g0073 others(63): Show |
66 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.127-300G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818007 | |||||||
| chr12:124818010 | C | T | 4 | a0001c0001t0003g0232 a0001c0017t0005g0341 a0001c0020t0003g0343 others(1): Show |
4 | HG02109.hp2 HG02572.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-303G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818010 | |||||||
| chr12:124818185 | C | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0281 |
2 | NA18982.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.127-478G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818185 | |||||||
| chr12:124818346 | T | C | 19 | a0001c0001t0003g0023 a0001c0001t0003g0029 a0001c0001t0003g0169 others(16): Show |
19 | HG01109.hp1 HG02145.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.127-639A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818346 | |||||||
| chr12:124818356 | C | G | 1 | a0001c0016t0001g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.127-649G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818356 | |||||||
| chr12:124818426 | G | A | 4 | a0001c0001t0003g0232 a0001c0017t0005g0341 a0001c0020t0003g0343 others(1): Show |
4 | HG02109.hp2 HG02572.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-719C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818426 | |||||||
| chr12:124818707 | G | A | 87 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0067 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.127-1000C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818707 | |||||||
| chr12:124818708 | C | T | 43 | a0001c0001t0001g0039 a0001c0001t0001g0080 a0001c0001t0001g0092 others(40): Show |
43 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.127-1001G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818708 | |||||||
| chr12:124818728 | CT | C | 187 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0052 others(184): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.127-1022delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818728 | |||||||
| chr12:124818736 | T | C | 229 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0052 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.127-1029A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818736 | |||||||
| chr12:124818771 | G | A | 2 | a0001c0007t0001g0090 a0001c0007t0005g0191 |
2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.127-1064C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818771 | |||||||
| chr12:124818863 | G | A | 1 | a0002c0006t0001g0004 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.127-1156C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818863 | |||||||
| chr12:124818979 | T | A | 89 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0067 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.127-1272A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124818979 | |||||||
| chr12:124819060 | G | A | 1 | a0001c0002t0005g0337 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.127-1353C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819060 | |||||||
| chr12:124819083 | C | T | 9 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0003g0020 others(6): Show |
9 | HG01884.hp1 HG02630.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-1376G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819083 | |||||||
| chr12:124819084 | G | A | 13 | a0001c0001t0003g0161 a0001c0001t0003g0226 a0001c0001t0004g0048 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-1377C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819084 | |||||||
| chr12:124819129 | T | TA | 63 | a0001c0001t0001g0130 a0001c0001t0002g0305 a0001c0003t0001g0098 others(60): Show |
63 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.127-1423dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819129 | |||||||
| chr12:124819129 | TA | T | 214 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0052 others(211): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.127-1423delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819129 | |||||||
| chr12:124819245 | G | A | 22 | a0001c0001t0003g0023 a0001c0001t0003g0029 a0001c0001t0003g0169 others(19): Show |
22 | HG01109.hp1 HG01433.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.127-1538C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819245 | |||||||
| chr12:124819248 | G | A | 1 | a0001c0002t0001g0081 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.127-1541C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819248 | |||||||
| chr12:124819288 | G | A | 1 | a0002c0006t0004g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-1581C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819288 | |||||||
| chr12:124819347 | T | C | 6 | a0001c0001t0003g0232 a0001c0001t0017g0028 a0001c0013t0016g0334 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-1640A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819347 | |||||||
| chr12:124819350 | G | A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0241 a0001c0001t0001g0242 others(2): Show |
5 | HG01099.hp2 HG01358.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-1643C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819350 | |||||||
| chr12:124819458 | C | T | 100 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0105 others(97): Show |
101 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.127-1751G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819458 | |||||||
| chr12:124819543 | C | T | 1 | a0001c0005t0003g0354 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.127-1836G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819543 | |||||||
| chr12:124819543 | CT | C | 62 | a0001c0001t0001g0130 a0001c0001t0002g0305 a0001c0001t0003g0114 others(59): Show |
62 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.127-1837delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819543 | |||||||
| chr12:124819682 | C | T | 4 | a0001c0001t0003g0086 a0001c0001t0003g0087 a0001c0001t0003g0089 others(1): Show |
4 | HG00280.hp2 HG00323.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-1975G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819682 | |||||||
| chr12:124819867 | C | A | 59 | a0001c0001t0001g0130 a0001c0001t0002g0305 a0001c0001t0003g0114 others(56): Show |
59 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.127-2160G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819867 | |||||||
| chr12:124819885 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.127-2178A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819885 | |||||||
| chr12:124819951 | G | A | 1 | a0001c0001t0006g0041 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.127-2244C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124819951 | |||||||
| chr12:124820160 | G | A | 1 | a0001c0002t0001g0327 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.127-2453C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124820160 | |||||||
| chr12:124820300 | C | G | 12 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0200 others(9): Show |
12 | HG00099.hp1 HG00280.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-2593G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124820300 | |||||||
| chr12:124820371 | T | C | 17 | a0001c0001t0003g0023 a0001c0001t0003g0029 a0001c0001t0003g0169 others(14): Show |
17 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.127-2664A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124820371 | |||||||
| chr12:124820457 | C | T | 2 | a0001c0004t0011g0119 a0001c0004t0014g0190 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.127-2750G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124820457 | |||||||
| chr12:124820480 | C | A | 1 | a0001c0002t0003g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127-2773G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124820480 | |||||||
| chr12:124820634 | C | A | 3 | a0001c0002t0003g0138 a0001c0002t0003g0139 a0001c0002t0003g0197 |
3 | HG03927.hp1 HG04199.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.127-2927G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124820634 | |||||||
| chr12:124820700 | C | A | 3 | a0001c0001t0003g0142 a0001c0001t0003g0284 a0001c0002t0001g0097 |
3 | HG02074.hp2 NA19000.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.127-2993G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124820700 | |||||||
| chr12:124820726 | G | A | 3 | a0001c0001t0003g0142 a0001c0001t0003g0284 a0001c0002t0001g0097 |
3 | HG02074.hp2 NA19000.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.127-3019C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124820726 | |||||||
| chr12:124820791 | G | A | 1 | a0001c0016t0001g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.127-3084C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124820791 | |||||||
| chr12:124820795 | G | A | 1 | a0001c0002t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.127-3088C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124820795 | |||||||
| chr12:124820857 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.127-3150G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124820857 | |||||||
| chr12:124821074 | C | T | 1 | a0002c0008t0001g0007 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.127-3367G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821074 | |||||||
| chr12:124821099 | G | A | 348 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(345): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.127-3392C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821099 | |||||||
| chr12:124821236 | T | TCA | 83 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0040 others(80): Show |
83 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.127-3531_127-3530d others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821236 | |||||||
| chr12:124821236 | T | TCACA | 5 | a0001c0001t0001g0251 a0001c0001t0002g0065 a0001c0001t0002g0244 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-3533_127-3530d others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821236 | |||||||
| chr12:124821236 | TCA | T | 87 | a0001c0001t0001g0130 a0001c0001t0001g0223 a0001c0001t0002g0305 others(84): Show |
87 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.127-3531_127-3530d others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821236 | |||||||
| chr12:124821236 | TCACA | T | 135 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0053 others(132): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.127-3533_127-3530d others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821236 | |||||||
| chr12:124821240 | A | T | 1 | a0001c0001t0008g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.127-3533T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821240 | |||||||
| chr12:124821433 | C | T | 40 | a0001c0001t0001g0034 a0001c0001t0003g0023 a0001c0001t0003g0029 others(37): Show |
40 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.127-3726G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821433 | |||||||
| chr12:124821477 | A | ATC | 42 | a0001c0001t0001g0034 a0001c0001t0003g0023 a0001c0001t0003g0029 others(39): Show |
42 | HG01070.hp1 HG01109.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.127-3772_127-3771d others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821477 | |||||||
| chr12:124821504 | A | G | 1 | a0004c0011t0002g0250 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.127-3797T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821504 | |||||||
| chr12:124821578 | C | A | 1 | a0001c0002t0001g0254 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.127-3871G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821578 | |||||||
| chr12:124821702 | G | A | 63 | a0001c0001t0001g0130 a0001c0001t0002g0305 a0001c0001t0003g0114 others(60): Show |
63 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.127-3995C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821702 | |||||||
| chr12:124821744 | G | A | 33 | a0001c0001t0001g0034 a0001c0001t0003g0023 a0001c0001t0003g0029 others(30): Show |
33 | HG01070.hp1 HG01109.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.127-4037C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821744 | |||||||
| chr12:124821787 | T | G | 1 | a0001c0002t0001g0101 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.127-4080A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821787 | |||||||
| chr12:124821794 | C | T | 1 | a0001c0002t0001g0248 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.127-4087G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821794 | |||||||
| chr12:124821937 | A | G | 348 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(345): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.127-4230T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124821937 | |||||||
| chr12:124822026 | C | T | 6 | a0001c0003t0001g0295 a0001c0003t0001g0296 a0001c0003t0002g0064 others(3): Show |
6 | NA18942.hp1 NA18957.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-4319G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124822026 | |||||||
| chr12:124822084 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.127-4377C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124822084 | |||||||
| chr12:124822192 | C | T | 1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.127-4485G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124822192 | |||||||
| chr12:124822253 | AT | A | 63 | a0001c0001t0001g0130 a0001c0001t0002g0305 a0001c0001t0003g0114 others(60): Show |
63 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.127-4547delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124822253 | |||||||
| chr12:124822302 | G | T | 63 | a0001c0001t0001g0130 a0001c0001t0002g0305 a0001c0001t0003g0114 others(60): Show |
63 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.127-4595C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124822302 | |||||||
| chr12:124822318 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.127-4611T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124822318 | |||||||
| chr12:124822444 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.127-4737C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124822444 | |||||||
| chr12:124822477 | G | C | 1 | a0001c0001t0001g0050 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.127-4770C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124822477 | |||||||
| chr12:124822507 | G | A | 38 | a0001c0001t0001g0039 a0001c0001t0001g0080 a0001c0001t0001g0092 others(35): Show |
38 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.127-4800C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124822507 | |||||||
| chr12:124822518 | G | A | 1 | a0001c0016t0001g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.127-4811C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124822518 | |||||||
| chr12:124822622 | C | T | 1 | a0003c0019t0011g0342 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.127-4915G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124822622 | |||||||
| chr12:124822884 | T | G | 24 | a0001c0001t0003g0023 a0001c0001t0003g0029 a0001c0001t0003g0169 others(21): Show |
24 | HG01109.hp1 HG01243.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.127-5177A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124822884 | |||||||
| chr12:124823143 | C | G | 27 | a0001c0001t0003g0114 a0001c0003t0001g0215 a0001c0003t0001g0262 others(24): Show |
27 | HG00544.hp1 HG00597.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.127-5436G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124823143 | |||||||
| chr12:124823325 | C | G | 288 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(285): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.127-5618G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124823325 | |||||||
| chr12:124823342 | G | T | 263 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(260): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.127-5635C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124823342 | |||||||
| chr12:124823388 | C | T | 1 | a0001c0002t0003g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.127-5681G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124823388 | |||||||
| chr12:124823476 | A | G | 1 | a0001c0004t0004g0230 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.127-5769T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124823476 | |||||||
| chr12:124823572 | G | A | 1 | a0001c0002t0001g0143 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.127-5865C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124823572 | |||||||
| chr12:124823715 | C | T | 6 | a0001c0001t0001g0034 a0001c0001t0005g0045 a0001c0001t0008g0046 others(3): Show |
6 | HG02717.hp2 HG02896.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-6008G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124823715 | |||||||
| chr12:124823716 | G | A | 1 | a0001c0002t0003g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127-6009C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124823716 | |||||||
| chr12:124823750 | C | T | 1 | a0001c0003t0002g0187 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.127-6043G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124823750 | |||||||
| chr12:124823815 | C | G | 347 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(344): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.127-6108G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124823815 | |||||||
| chr12:124823902 | C | T | 3 | a0001c0001t0003g0267 a0001c0003t0002g0273 a0001c0003t0007g0274 |
3 | HG00597.hp2 NA18982.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.127-6195G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124823902 | |||||||
| chr12:124823962 | C | A | 3 | a0002c0006t0004g0012 a0003c0009t0003g0123 a0003c0019t0011g0342 |
3 | HG02572.hp1 HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-6255G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124823962 | |||||||
| chr12:124824009 | A | T | 2 | a0001c0001t0001g0200 a0001c0002t0005g0079 |
2 | HG00099.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.127-6302T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824009 | |||||||
| chr12:124824011 | A | T | 101 | a0001c0001t0001g0034 a0001c0001t0001g0052 a0001c0001t0001g0053 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.127-6304T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824011 | |||||||
| chr12:124824012 | ATAT | A | 18 | a0001c0001t0003g0023 a0001c0001t0003g0029 a0001c0001t0003g0169 others(15): Show |
18 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.127-6308_127-6306d others(5): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824012 | |||||||
| chr12:124824013 | T | A | 94 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0050 others(91): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.127-6306A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824013 | |||||||
| chr12:124824015 | T | A | 94 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0050 others(91): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.127-6308A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824015 | |||||||
| chr12:124824018 | A | G | 112 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0050 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.127-6311T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824018 | |||||||
| chr12:124824020 | A | G | 14 | a0001c0001t0001g0034 a0001c0001t0005g0045 a0001c0001t0008g0046 others(11): Show |
14 | HG01433.hp1 HG01928.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-6313T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824020 | |||||||
| chr12:124824051 | G | A | 1 | a0001c0004t0002g0271 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.127-6344C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824051 | |||||||
| chr12:124824067 | G | A | 1 | a0002c0006t0006g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-6360C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824067 | |||||||
| chr12:124824105 | C | T | 6 | a0001c0001t0001g0034 a0001c0001t0005g0045 a0001c0001t0008g0046 others(3): Show |
6 | HG02717.hp2 HG02896.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-6398G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824105 | |||||||
| chr12:124824136 | G | A | 200 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0050 others(197): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.127-6429C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824136 | |||||||
| chr12:124824175 | C | CA | 8 | a0001c0001t0003g0232 a0001c0001t0004g0048 a0001c0001t0006g0118 others(5): Show |
8 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-6469dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824175 | |||||||
| chr12:124824175 | CA | C | 195 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0050 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.127-6469delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824175 | |||||||
| chr12:124824190 | A | AAG | 7 | a0001c0001t0003g0025 a0001c0001t0012g0060 a0001c0001t0012g0062 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-6485_127-6484d others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824190 | |||||||
| chr12:124824190 | A | AG | 33 | a0001c0001t0001g0039 a0001c0001t0001g0080 a0001c0001t0001g0092 others(30): Show |
33 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.127-6484_127-6483i others(3): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824190 | |||||||
| chr12:124824403 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.127-6696C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824403 | |||||||
| chr12:124824417 | C | T | 75 | a0001c0001t0001g0130 a0001c0001t0001g0184 a0001c0001t0001g0186 others(72): Show |
75 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.127-6710G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824417 | |||||||
| chr12:124824464 | C | A | 1 | a0002c0008t0003g0015 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.127-6757G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824464 | |||||||
| chr12:124824469 | C | A | 1 | a0001c0002t0001g0177 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.127-6762G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824469 | |||||||
| chr12:124824936 | G | A | 4 | a0001c0018t0006g0340 a0002c0006t0004g0012 a0003c0009t0003g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-7229C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824936 | |||||||
| chr12:124824962 | C | T | 89 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0050 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.127-7255G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824962 | |||||||
| chr12:124824963 | G | A | 17 | a0001c0001t0001g0034 a0001c0001t0003g0161 a0001c0001t0003g0226 others(14): Show |
17 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.127-7256C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124824963 | |||||||
| chr12:124825068 | C | CA | 5 | a0001c0002t0001g0332 a0001c0002t0007g0058 a0001c0002t0007g0201 others(2): Show |
5 | HG01433.hp1 HG01928.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-7362dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825068 | |||||||
| chr12:124825108 | C | T | 86 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0094 others(83): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.127-7401G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825108 | |||||||
| chr12:124825156 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.127-7449G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825156 | |||||||
| chr12:124825185 | A | G | 1 | a0001c0005t0004g0353 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.127-7478T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825185 | |||||||
| chr12:124825224 | CA | C | 303 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0040 others(300): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.127-7518delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825224 | |||||||
| chr12:124825224 | CAA | C | 30 | a0001c0001t0001g0019 a0001c0001t0001g0094 a0001c0001t0001g0184 others(27): Show |
30 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.127-7519_127-7518d others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825224 | |||||||
| chr12:124825224 | CAAAAAAA others(4): Show |
C | 1 | a0001c0003t0002g0172 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.127-7528_127-7518d others(13): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825224 | |||||||
| chr12:124825280 | C | G | 1 | a0001c0001t0002g0335 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.127-7573G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825280 | |||||||
| chr12:124825446 | G | A | 18 | a0001c0001t0003g0023 a0001c0001t0003g0029 a0001c0001t0003g0169 others(15): Show |
18 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.127-7739C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825446 | |||||||
| chr12:124825499 | C | T | 3 | a0001c0003t0002g0131 a0001c0003t0002g0317 a0001c0007t0003g0135 |
3 | HG00438.hp2 HG02040.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.127-7792G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825499 | |||||||
| chr12:124825521 | A | C | 4 | a0001c0001t0005g0045 a0001c0001t0008g0046 a0001c0004t0015g0044 others(1): Show |
4 | HG02717.hp2 HG02896.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-7814T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825521 | |||||||
| chr12:124825563 | C | T | 18 | a0001c0001t0003g0023 a0001c0001t0003g0029 a0001c0001t0003g0169 others(15): Show |
18 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.127-7856G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825563 | |||||||
| chr12:124825603 | G | A | 1 | a0001c0002t0001g0314 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.127-7896C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825603 | |||||||
| chr12:124825759 | G | A | 73 | a0001c0001t0001g0130 a0001c0001t0001g0184 a0001c0001t0001g0186 others(70): Show |
73 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.127-8052C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825759 | |||||||
| chr12:124825792 | A | T | 1 | a0004c0011t0002g0250 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.127-8085T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825792 | |||||||
| chr12:124825807 | G | A | 2 | a0001c0001t0006g0118 a0001c0001t0006g0120 |
2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.127-8100C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825807 | |||||||
| chr12:124825822 | C | T | 1 | a0002c0006t0001g0002 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.127-8115G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124825822 | |||||||
| chr12:124826200 | G | A | 1 | a0001c0002t0003g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127-8493C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826200 | |||||||
| chr12:124826279 | C | T | 1 | a0001c0001t0005g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.127-8572G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826279 | |||||||
| chr12:124826308 | G | A | 5 | a0001c0002t0001g0332 a0001c0002t0007g0058 a0001c0002t0007g0201 others(2): Show |
5 | HG01433.hp1 HG01928.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-8601C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826308 | |||||||
| chr12:124826317 | C | T | 17 | a0001c0001t0001g0034 a0001c0001t0003g0161 a0001c0001t0003g0226 others(14): Show |
17 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.127-8610G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826317 | |||||||
| chr12:124826330 | C | CA | 145 | a0001c0001t0001g0039 a0001c0001t0001g0080 a0001c0001t0001g0092 others(142): Show |
145 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.127-8624dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826330 | |||||||
| chr12:124826330 | CA | C | 12 | a0001c0001t0003g0161 a0001c0001t0003g0226 a0001c0001t0004g0121 others(9): Show |
12 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-8624delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826330 | |||||||
| chr12:124826493 | C | T | 1 | a0001c0003t0002g0187 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.127-8786G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826493 | |||||||
| chr12:124826494 | G | T | 40 | a0001c0001t0001g0034 a0001c0001t0003g0023 a0001c0001t0003g0029 others(37): Show |
40 | HG01109.hp1 HG01433.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.127-8787C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826494 | |||||||
| chr12:124826529 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.127-8822C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826529 | |||||||
| chr12:124826608 | CTATTTTT others(1): Show |
C | 3 | a0001c0002t0001g0081 a0001c0003t0002g0291 a0001c0003t0002g0299 |
3 | HG00140.hp1 HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.127-8909_127-8902d others(10): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826608 | |||||||
| chr12:124826753 | C | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0185 a0002c0006t0003g0008 |
3 | HG00738.hp2 HG01515.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.127-9046G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826753 | |||||||
| chr12:124826785 | A | C | 4 | a0001c0018t0006g0340 a0002c0006t0004g0012 a0003c0009t0003g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-9078T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826785 | |||||||
| chr12:124826960 | G | C | 73 | a0001c0001t0001g0130 a0001c0001t0001g0184 a0001c0001t0001g0186 others(70): Show |
73 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.127-9253C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124826960 | |||||||
| chr12:124827042 | A | G | 2 | a0001c0001t0006g0118 a0001c0001t0006g0120 |
2 | HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.127-9335T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827042 | |||||||
| chr12:124827174 | C | T | 22 | a0001c0001t0001g0034 a0001c0001t0001g0080 a0001c0001t0001g0152 others(19): Show |
22 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-9467G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827174 | |||||||
| chr12:124827218 | A | G | 1 | a0001c0007t0001g0063 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.127-9511T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827218 | |||||||
| chr12:124827310 | T | C | 18 | a0001c0001t0003g0023 a0001c0001t0003g0029 a0001c0001t0003g0169 others(15): Show |
18 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.127-9603A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827310 | |||||||
| chr12:124827388 | C | T | 32 | a0001c0001t0001g0072 a0001c0001t0001g0112 a0001c0001t0001g0145 others(29): Show |
32 | HG00140.hp2 HG01123.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.127-9681G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827388 | |||||||
| chr12:124827401 | G | C | 2 | a0001c0002t0001g0219 a0001c0002t0001g0248 |
2 | NA18953.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.127-9694C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827401 | |||||||
| chr12:124827413 | A | ATAT | 5 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
5 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-9709_127-9707d others(5): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827413 | |||||||
| chr12:124827413 | ATAT | A | 121 | a0001c0001t0001g0034 a0001c0001t0001g0130 a0001c0001t0001g0184 others(118): Show |
121 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.127-9709_127-9707d others(5): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827413 | |||||||
| chr12:124827527 | C | G | 223 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(220): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.127-9820G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827527 | |||||||
| chr12:124827657 | C | G | 19 | a0001c0001t0001g0094 a0001c0001t0001g0199 a0001c0001t0002g0104 others(16): Show |
19 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.127-9950G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827657 | |||||||
| chr12:124827658 | C | T | 345 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(342): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.127-9951G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827658 | |||||||
| chr12:124827805 | G | A | 1 | a0001c0003t0002g0275 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.127-10098C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827805 | |||||||
| chr12:124827813 | G | A | 8 | a0001c0001t0005g0045 a0001c0001t0008g0046 a0001c0004t0015g0044 others(5): Show |
8 | HG02572.hp1 HG02717.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-10106C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827813 | |||||||
| chr12:124827849 | C | T | 101 | a0001c0001t0001g0034 a0001c0001t0001g0130 a0001c0001t0001g0184 others(98): Show |
101 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.127-10142G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827849 | |||||||
| chr12:124827879 | G | C | 163 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0080 others(160): Show |
163 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.127-10172C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827879 | |||||||
| chr12:124827989 | A | G | 2 | a0001c0001t0016g0240 a0001c0005t0004g0353 |
2 | HG01243.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.127-10282T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124827989 | |||||||
| chr12:124828045 | T | C | 5 | a0001c0002t0001g0332 a0001c0002t0007g0058 a0001c0002t0007g0201 others(2): Show |
5 | HG01433.hp1 HG01928.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-10338A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124828045 | |||||||
| chr12:124828066 | G | C | 144 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0053 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.127-10359C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124828066 | |||||||
| chr12:124828434 | C | T | 1 | a0001c0001t0003g0246 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.127-10727G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124828434 | |||||||
| chr12:124828508 | G | A | 1 | a0001c0003t0002g0136 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.127-10801C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124828508 | |||||||
| chr12:124828513 | A | G | 247 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.127-10806T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124828513 | |||||||
| chr12:124828527 | G | A | 203 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0040 others(200): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.127-10820C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124828527 | |||||||
| chr12:124828792 | G | A | 22 | a0001c0001t0001g0112 a0001c0001t0001g0318 a0001c0001t0002g0065 others(19): Show |
22 | HG00140.hp2 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-11085C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124828792 | |||||||
| chr12:124828880 | C | T | 81 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0050 others(78): Show |
81 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.127-11173G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124828880 | |||||||
| chr12:124829316 | G | A | 2 | a0001c0001t0002g0316 a0001c0004t0004g0195 |
2 | NA18965.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.127-11609C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124829316 | |||||||
| chr12:124829326 | C | T | 103 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0050 others(100): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.127-11619G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124829326 | |||||||
| chr12:124829354 | C | A | 247 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.127-11647G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124829354 | |||||||
| chr12:124829488 | A | C | 1 | a0001c0001t0002g0234 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.127-11781T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124829488 | |||||||
| chr12:124829550 | C | T | 73 | a0001c0001t0001g0130 a0001c0001t0001g0184 a0001c0001t0001g0186 others(70): Show |
73 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.127-11843G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124829550 | |||||||
| chr12:124829555 | ACT | A | 80 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0050 others(77): Show |
80 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.127-11850_127-1184 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124829555 | |||||||
| chr12:124829570 | C | T | 3 | a0001c0002t0005g0336 a0001c0002t0005g0337 a0001c0002t0005g0338 |
3 | HG03491.hp1 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.127-11863G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124829570 | |||||||
| chr12:124829620 | C | T | 2 | a0001c0001t0016g0240 a0001c0005t0004g0353 |
2 | HG01243.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.127-11913G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124829620 | |||||||
| chr12:124829868 | A | G | 247 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.127-12161T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124829868 | |||||||
| chr12:124830042 | G | A | 3 | a0001c0001t0003g0087 a0001c0001t0016g0240 a0001c0005t0004g0353 |
3 | HG00280.hp2 HG01243.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.127-12335C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830042 | |||||||
| chr12:124830328 | C | G | 2 | a0001c0001t0016g0240 a0001c0005t0004g0353 |
2 | HG01243.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.127-12621G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830328 | |||||||
| chr12:124830369 | A | C | 1 | a0001c0002t0003g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.127-12662T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830369 | |||||||
| chr12:124830375 | A | G | 247 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.127-12668T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830375 | |||||||
| chr12:124830401 | G | A | 1 | a0001c0001t0002g0096 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.127-12694C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830401 | |||||||
| chr12:124830437 | T | C | 247 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.127-12730A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830437 | |||||||
| chr12:124830476 | C | T | 1 | a0001c0004t0003g0203 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.127-12769G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830476 | |||||||
| chr12:124830500 | A | C | 247 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.127-12793T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830500 | |||||||
| chr12:124830562 | G | A | 1 | a0001c0002t0001g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.127-12855C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830562 | |||||||
| chr12:124830660 | G | T | 1 | a0002c0008t0001g0009 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.127-12953C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830660 | |||||||
| chr12:124830746 | C | A | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0176 |
3 | HG00738.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.127-13039G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830746 | |||||||
| chr12:124830746 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.127-13039G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830746 | |||||||
| chr12:124830770 | C | T | 247 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.127-13063G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830770 | |||||||
| chr12:124830835 | C | T | 247 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.127-13128G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830835 | |||||||
| chr12:124830852 | G | A | 7 | a0001c0001t0003g0025 a0001c0001t0012g0060 a0001c0001t0012g0062 others(4): Show |
7 | HG02109.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-13145C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830852 | |||||||
| chr12:124830908 | G | A | 247 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.127-13201C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830908 | |||||||
| chr12:124830961 | C | T | 247 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.127-13254G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830961 | |||||||
| chr12:124830963 | C | T | 1 | a0001c0004t0014g0190 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.127-13256G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830963 | |||||||
| chr12:124830979 | A | AT | 75 | a0001c0001t0001g0130 a0001c0001t0001g0184 a0001c0001t0001g0186 others(72): Show |
75 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.127-13273dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830979 | |||||||
| chr12:124830979 | A | ATT | 149 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(146): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.127-13274_127-1327 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830979 | |||||||
| chr12:124830979 | A | ATTT | 23 | a0001c0001t0003g0023 a0001c0001t0003g0029 a0001c0001t0003g0169 others(20): Show |
23 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.127-13275_127-1327 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124830979 | |||||||
| chr12:124831015 | A | G | 247 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.127-13308T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831015 | |||||||
| chr12:124831038 | C | T | 104 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0050 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.127-13331G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831038 | |||||||
| chr12:124831045 | G | A | 247 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(244): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.127-13338C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831045 | |||||||
| chr12:124831059 | T | C | 4 | a0001c0018t0006g0340 a0002c0006t0004g0012 a0003c0009t0003g0123 others(1): Show |
4 | HG02572.hp1 HG02965.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-13352A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831059 | |||||||
| chr12:124831101 | A | G | 144 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0080 others(141): Show |
144 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.127-13394T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831101 | |||||||
| chr12:124831124 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0185 a0002c0006t0003g0008 |
3 | HG00738.hp2 HG01515.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.127-13417G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831124 | |||||||
| chr12:124831192 | T | G | 4 | a0001c0001t0003g0117 a0001c0001t0003g0239 a0001c0001t0005g0043 others(1): Show |
4 | HG02622.hp1 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-13485A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831192 | |||||||
| chr12:124831443 | T | G | 169 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(166): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.127-13736A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831443 | |||||||
| chr12:124831485 | G | T | 61 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0080 others(58): Show |
61 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.127-13778C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831485 | |||||||
| chr12:124831509 | A | C | 43 | a0001c0001t0001g0039 a0001c0001t0001g0080 a0001c0001t0001g0092 others(40): Show |
43 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.127-13802T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831509 | |||||||
| chr12:124831606 | G | A | 36 | a0001c0001t0001g0034 a0001c0001t0003g0023 a0001c0001t0003g0029 others(33): Show |
36 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.127-13899C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831606 | |||||||
| chr12:124831670 | C | A | 1 | a0001c0002t0001g0256 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.127-13963G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831670 | |||||||
| chr12:124831734 | T | C | 96 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0067 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.127-14027A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831734 | |||||||
| chr12:124831889 | G | T | 1 | a0001c0001t0001g0039 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.127-14182C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831889 | |||||||
| chr12:124831969 | G | T | 3 | a0001c0001t0002g0292 a0001c0001t0002g0335 a0001c0004t0001g0099 |
3 | NA18970.hp1 NA18983.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.127-14262C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124831969 | |||||||
| chr12:124832104 | T | C | 10 | a0001c0001t0001g0067 a0001c0001t0001g0194 a0001c0001t0001g0326 others(7): Show |
10 | HG00609.hp2 HG02523.hp1 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-14397A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832104 | |||||||
| chr12:124832114 | T | G | 96 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0067 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.127-14407A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832114 | |||||||
| chr12:124832197 | C | T | 65 | a0001c0001t0001g0039 a0001c0001t0001g0080 a0001c0001t0001g0092 others(62): Show |
65 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.127-14490G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832197 | |||||||
| chr12:124832224 | T | C | 144 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0053 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.127-14517A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832224 | |||||||
| chr12:124832243 | C | T | 1 | a0002c0008t0003g0015 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.127-14536G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832243 | |||||||
| chr12:124832407 | C | T | 1 | a0001c0002t0001g0227 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.127-14700G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832407 | |||||||
| chr12:124832517 | C | G | 148 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0053 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.127-14810G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832517 | |||||||
| chr12:124832519 | C | CA | 241 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0040 others(238): Show |
241 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.127-14813dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832519 | |||||||
| chr12:124832519 | C | CAA | 12 | a0001c0001t0001g0019 a0001c0001t0002g0116 a0001c0001t0003g0165 others(9): Show |
12 | HG00597.hp2 HG01928.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-14814_127-1481 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832519 | |||||||
| chr12:124832520 | A | C | 5 | a0001c0002t0001g0151 a0001c0002t0003g0138 a0001c0002t0003g0139 others(2): Show |
5 | HG01074.hp1 HG03239.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-14813T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832520 | |||||||
| chr12:124832579 | G | A | 41 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0094 others(38): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.127-14872C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832579 | |||||||
| chr12:124832684 | G | A | 330 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(327): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.127-14977C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832684 | |||||||
| chr12:124832701 | A | G | 52 | a0001c0001t0001g0067 a0001c0001t0001g0199 a0001c0001t0001g0301 others(49): Show |
52 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.127-14994T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832701 | |||||||
| chr12:124832845 | C | A | 132 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0080 others(129): Show |
133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.127-15138G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832845 | |||||||
| chr12:124832895 | T | C | 66 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0092 others(63): Show |
66 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.127-15188A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832895 | |||||||
| chr12:124832909 | C | T | 1 | a0002c0006t0004g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-15202G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832909 | |||||||
| chr12:124832912 | G | C | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0038 others(1): Show |
4 | HG01361.hp1 HG02615.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-15205C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832912 | |||||||
| chr12:124832915 | G | A | 1 | a0001c0001t0004g0026 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.127-15208C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832915 | |||||||
| chr12:124832958 | A | G | 51 | a0001c0001t0001g0159 a0001c0001t0001g0199 a0001c0001t0001g0200 others(48): Show |
51 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.127-15251T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124832958 | |||||||
| chr12:124833036 | C | T | 150 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0052 others(147): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.127-15329G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833036 | |||||||
| chr12:124833143 | T | C | 13 | a0001c0001t0001g0146 a0001c0001t0001g0162 a0001c0001t0003g0161 others(10): Show |
13 | HG01175.hp1 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-15436A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833143 | |||||||
| chr12:124833193 | C | CT | 148 | a0001c0001t0001g0034 a0001c0001t0001g0040 a0001c0001t0001g0050 others(145): Show |
148 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.127-15487dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833193 | |||||||
| chr12:124833193 | CT | C | 12 | a0001c0001t0003g0038 a0001c0001t0003g0232 a0001c0001t0004g0026 others(9): Show |
12 | HG01361.hp1 HG01884.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-15487delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833193 | |||||||
| chr12:124833193 | CTT | C | 78 | a0001c0001t0001g0019 a0001c0001t0001g0072 a0001c0001t0001g0130 others(75): Show |
78 | HG00140.hp1 HG00621.hp1 HG01070.hp1 others(75): Show |
intron_variant | MODIFIER | c.127-15488_127-1548 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833193 | |||||||
| chr12:124833204 | T | C | 3 | a0001c0001t0006g0031 a0001c0001t0006g0035 a0001c0001t0008g0036 |
3 | HG03486.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.127-15497A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833204 | |||||||
| chr12:124833275 | G | A | 15 | a0001c0001t0003g0117 a0001c0001t0003g0165 a0001c0001t0004g0121 others(12): Show |
15 | HG01243.hp1 HG01891.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-15568C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833275 | |||||||
| chr12:124833336 | T | C | 302 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(299): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.127-15629A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833336 | |||||||
| chr12:124833395 | G | A | 86 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0132 others(83): Show |
86 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.127-15688C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833395 | |||||||
| chr12:124833599 | T | C | 10 | a0001c0001t0003g0267 a0001c0002t0001g0081 a0001c0002t0001g0254 others(7): Show |
10 | HG00140.hp1 HG00621.hp1 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-15892A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833599 | |||||||
| chr12:124833707 | C | T | 76 | a0001c0001t0001g0072 a0001c0001t0001g0186 a0001c0001t0001g0198 others(73): Show |
76 | HG00609.hp2 HG00621.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.127-16000G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833707 | |||||||
| chr12:124833738 | G | A | 1 | a0001c0001t0003g0260 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.127-16031C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833738 | |||||||
| chr12:124833763 | C | T | 172 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(169): Show |
173 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.127-16056G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833763 | |||||||
| chr12:124833809 | G | A | 1 | a0001c0004t0001g0277 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.127-16102C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833809 | |||||||
| chr12:124833825 | C | T | 15 | a0001c0001t0001g0186 a0001c0001t0001g0198 a0001c0001t0001g0206 others(12): Show |
15 | HG01069.hp2 HG01074.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-16118G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833825 | |||||||
| chr12:124833859 | T | C | 1 | a0001c0001t0002g0221 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.127-16152A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833859 | |||||||
| chr12:124833902 | G | C | 167 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(164): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.127-16195C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833902 | |||||||
| chr12:124833915 | A | G | 173 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(170): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.127-16208T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124833915 | |||||||
| chr12:124834030 | C | T | 1 | a0001c0003t0002g0300 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.127-16323G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834030 | |||||||
| chr12:124834075 | G | A | 1 | a0001c0003t0002g0212 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.127-16368C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834075 | |||||||
| chr12:124834082 | G | A | 1 | a0001c0001t0004g0026 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.127-16375C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834082 | |||||||
| chr12:124834121 | T | C | 1 | a0001c0001t0008g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-16414A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834121 | |||||||
| chr12:124834226 | C | T | 170 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(167): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.127-16519G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834226 | |||||||
| chr12:124834593 | T | C | 167 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(164): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.127-16886A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834593 | |||||||
| chr12:124834635 | T | C | 16 | a0001c0001t0001g0152 a0001c0001t0005g0045 a0001c0001t0008g0046 others(13): Show |
16 | HG00639.hp1 HG01106.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.127-16928A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834635 | |||||||
| chr12:124834679 | A | G | 167 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(164): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.127-16972T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834679 | |||||||
| chr12:124834694 | G | C | 167 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(164): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.127-16987C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834694 | |||||||
| chr12:124834847 | G | A | 5 | a0001c0001t0003g0038 a0001c0001t0003g0239 a0001c0001t0005g0047 others(2): Show |
5 | HG01361.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-17140C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834847 | |||||||
| chr12:124834909 | C | T | 166 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(163): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.127-17202G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834909 | |||||||
| chr12:124834911 | C | T | 3 | a0001c0001t0001g0326 a0001c0001t0002g0234 a0001c0002t0001g0236 |
3 | NA18948.hp2 NA18990.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.127-17204G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834911 | |||||||
| chr12:124834914 | C | A | 3 | a0001c0001t0017g0030 a0001c0005t0006g0344 a0003c0019t0011g0342 |
3 | HG02055.hp1 HG02109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.127-17207G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834914 | |||||||
| chr12:124834915 | A | C | 50 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0152 others(47): Show |
51 | HG00639.hp1 HG00673.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.127-17208T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834915 | |||||||
| chr12:124834935 | A | T | 1 | a0001c0002t0003g0249 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.127-17228T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124834935 | |||||||
| chr12:124835074 | A | G | 3 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0003c0009t0001g0222 |
3 | HG02056.hp2 HG02738.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.127-17367T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835074 | |||||||
| chr12:124835225 | G | A | 166 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(163): Show |
167 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.127-17518C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835225 | |||||||
| chr12:124835256 | G | A | 5 | a0001c0001t0003g0232 a0001c0001t0006g0022 a0001c0001t0008g0233 others(2): Show |
5 | HG02559.hp2 HG02572.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-17549C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835256 | |||||||
| chr12:124835262 | A | AT | 27 | a0001c0001t0001g0019 a0001c0001t0002g0157 a0001c0001t0003g0020 others(24): Show |
27 | HG01168.hp2 HG01243.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.127-17556dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835262 | |||||||
| chr12:124835262 | A | ATT | 140 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0072 others(137): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.127-17557_127-1755 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835262 | |||||||
| chr12:124835291 | C | T | 165 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(162): Show |
166 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.127-17584G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835291 | |||||||
| chr12:124835428 | T | A | 1 | a0001c0001t0006g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.127-17721A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835428 | |||||||
| chr12:124835433 | CATTTTTT others(9): Show |
C | 1 | a0001c0002t0001g0049 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.127-17742_127-1772 others(20): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835433 | |||||||
| chr12:124835609 | T | G | 64 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0132 others(61): Show |
64 | HG00438.hp1 HG00639.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.127-17902A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835609 | |||||||
| chr12:124835641 | T | TA | 49 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(46): Show |
49 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.127-17935dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835641 | |||||||
| chr12:124835713 | T | G | 327 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(324): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.127-18006A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835713 | |||||||
| chr12:124835845 | T | C | 337 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(334): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.127-18138A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835845 | |||||||
| chr12:124835846 | G | A | 6 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0003g0161 others(3): Show |
6 | HG02922.hp2 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-18139C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835846 | |||||||
| chr12:124835863 | G | A | 1 | a0001c0001t0008g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-18156C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835863 | |||||||
| chr12:124835920 | G | A | 1 | a0001c0001t0008g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-18213C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124835920 | |||||||
| chr12:124836017 | C | T | 64 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0132 others(61): Show |
64 | HG00438.hp1 HG00639.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.127-18310G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836017 | |||||||
| chr12:124836032 | T | C | 64 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0132 others(61): Show |
64 | HG00438.hp1 HG00639.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.127-18325A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836032 | |||||||
| chr12:124836104 | G | A | 6 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0003g0161 others(3): Show |
6 | HG02922.hp2 HG02965.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-18397C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836104 | |||||||
| chr12:124836125 | G | C | 1 | a0001c0003t0001g0215 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.127-18418C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836125 | |||||||
| chr12:124836137 | C | A | 1 | a0001c0001t0008g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-18430G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836137 | |||||||
| chr12:124836169 | C | T | 163 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(160): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.127-18462G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836169 | |||||||
| chr12:124836282 | A | G | 233 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(230): Show |
234 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.127-18575T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836282 | |||||||
| chr12:124836286 | C | T | 1 | a0002c0008t0001g0009 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.127-18579G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836286 | |||||||
| chr12:124836304 | C | T | 163 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(160): Show |
164 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.127-18597G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836304 | |||||||
| chr12:124836404 | A | T | 6 | a0001c0001t0003g0232 a0001c0001t0004g0324 a0001c0001t0006g0022 others(3): Show |
6 | HG02559.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-18697T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836404 | |||||||
| chr12:124836478 | G | A | 4 | a0001c0001t0003g0038 a0001c0001t0003g0239 a0001c0001t0005g0047 others(1): Show |
4 | HG01361.hp1 HG02145.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-18771C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836478 | |||||||
| chr12:124836651 | A | G | 47 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(44): Show |
47 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.127-18944T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836651 | |||||||
| chr12:124836653 | A | G | 243 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(240): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.127-18946T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836653 | |||||||
| chr12:124836748 | C | T | 149 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(146): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.127-19041G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836748 | |||||||
| chr12:124836837 | T | C | 148 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(145): Show |
149 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.127-19130A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836837 | |||||||
| chr12:124836844 | A | G | 6 | a0001c0001t0003g0232 a0001c0001t0004g0324 a0001c0001t0006g0022 others(3): Show |
6 | HG02559.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-19137T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836844 | |||||||
| chr12:124836915 | T | G | 149 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(146): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.127-19208A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836915 | |||||||
| chr12:124836944 | C | CAT | 149 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(146): Show |
150 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.127-19238_127-1923 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836944 | |||||||
| chr12:124836985 | G | A | 148 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(145): Show |
149 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.127-19278C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124836985 | |||||||
| chr12:124837010 | C | A | 1 | a0001c0002t0007g0216 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.127-19303G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837010 | |||||||
| chr12:124837010 | C | T | 3 | a0001c0001t0002g0310 a0001c0002t0001g0302 a0001c0002t0001g0303 |
3 | HG00609.hp2 NA19056.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.127-19303G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837010 | |||||||
| chr12:124837051 | G | A | 1 | a0001c0001t0008g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-19344C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837051 | |||||||
| chr12:124837074 | C | T | 148 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(145): Show |
149 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.127-19367G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837074 | |||||||
| chr12:124837103 | A | T | 148 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(145): Show |
149 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.127-19396T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837103 | |||||||
| chr12:124837221 | G | A | 5 | a0001c0001t0003g0038 a0001c0001t0003g0239 a0001c0001t0005g0047 others(2): Show |
5 | HG01361.hp1 HG02145.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-19514C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837221 | |||||||
| chr12:124837380 | G | A | 1 | a0001c0002t0001g0311 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.127-19673C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837380 | |||||||
| chr12:124837398 | T | A | 1 | a0001c0001t0008g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-19691A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837398 | |||||||
| chr12:124837468 | A | G | 8 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0003g0161 others(5): Show |
8 | HG02717.hp2 HG02723.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-19761T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837468 | |||||||
| chr12:124837468 | AAAGAAAG others(1): Show |
A | 70 | a0001c0001t0001g0034 a0001c0001t0001g0050 a0001c0001t0001g0052 others(67): Show |
70 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.127-19769_127-1976 others(12): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837468 | |||||||
| chr12:124837468 | AAAGAAAG others(5): Show |
A | 33 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0228 others(30): Show |
33 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.127-19773_127-1976 others(16): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837468 | |||||||
| chr12:124837472 | A | AAAGG | 10 | a0001c0001t0001g0251 a0001c0001t0002g0096 a0001c0001t0002g0157 others(7): Show |
10 | HG02074.hp1 HG02486.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-19769_127-1976 others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837472 | |||||||
| chr12:124837472 | A | AAAGGAAG others(1): Show |
4 | a0001c0001t0003g0232 a0001c0001t0008g0233 a0001c0001t0008g0331 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-19773_127-1976 others(12): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837472 | |||||||
| chr12:124837472 | A | AAAGGAAG others(13): Show |
3 | a0001c0001t0003g0038 a0001c0001t0003g0239 a0001c0001t0005g0047 |
3 | HG01361.hp1 HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.127-19785_127-1976 others(24): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837472 | |||||||
| chr12:124837472 | A | G | 94 | a0001c0001t0001g0019 a0001c0001t0001g0072 a0001c0001t0001g0152 others(91): Show |
94 | HG00609.hp2 HG00621.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.127-19765T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837472 | |||||||
| chr12:124837472 | AAAGG | A | 24 | a0001c0001t0001g0144 a0001c0001t0003g0086 a0001c0001t0003g0087 others(21): Show |
25 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.127-19769_127-1976 others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837472 | |||||||
| chr12:124837497 | A | G | 1 | a0003c0009t0003g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.127-19790T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837497 | |||||||
| chr12:124837503 | GGGA | G | 7 | a0001c0001t0003g0020 a0001c0001t0003g0165 a0001c0001t0008g0027 others(4): Show |
7 | HG02572.hp1 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-19799_127-1979 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837503 | |||||||
| chr12:124837504 | GGAGAAAA | G | 10 | a0001c0001t0001g0152 a0001c0001t0003g0025 a0001c0001t0003g0029 others(7): Show |
10 | HG00639.hp1 HG01106.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-19804_127-1979 others(11): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837504 | |||||||
| chr12:124837504 | GGAGAAAA others(5): Show |
G | 3 | a0001c0001t0003g0140 a0001c0001t0003g0142 a0001c0001t0006g0022 |
3 | HG03041.hp2 NA18971.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.127-19809_127-1979 others(16): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837504 | |||||||
| chr12:124837505 | G | A | 95 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0072 others(92): Show |
95 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.127-19798C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837505 | |||||||
| chr12:124837506 | A | AG | 5 | a0001c0001t0001g0019 a0001c0001t0003g0161 a0001c0016t0001g0021 others(2): Show |
5 | HG02109.hp2 HG03453.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-19800dupC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837506 | |||||||
| chr12:124837507 | G | A | 1 | a0003c0009t0003g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.127-19800C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837507 | |||||||
| chr12:124837507 | GA | G | 39 | a0001c0001t0001g0072 a0001c0001t0001g0173 a0001c0001t0001g0174 others(36): Show |
39 | HG00609.hp2 HG00738.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.127-19801delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837507 | |||||||
| chr12:124837507 | GAAAAAAG others(1): Show |
G | 13 | a0001c0001t0001g0132 a0001c0001t0001g0281 a0001c0001t0008g0126 others(10): Show |
13 | HG01884.hp1 HG02165.hp2 HG03471.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-19808_127-1980 others(12): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837507 | |||||||
| chr12:124837508 | A | G | 38 | a0001c0001t0001g0039 a0001c0001t0001g0272 a0001c0001t0002g0115 others(35): Show |
38 | HG00438.hp1 HG00621.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.127-19801T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837508 | |||||||
| chr12:124837509 | A | AAGG | 16 | a0001c0001t0001g0272 a0001c0001t0002g0115 a0001c0001t0002g0116 others(13): Show |
16 | HG00621.hp2 HG02056.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.127-19803_127-1980 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837509 | |||||||
| chr12:124837509 | A | G | 52 | a0001c0001t0001g0072 a0001c0001t0001g0173 a0001c0001t0001g0174 others(49): Show |
52 | HG00609.hp2 HG00738.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.127-19802T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837509 | |||||||
| chr12:124837510 | A | AGG | 3 | a0001c0001t0008g0125 a0001c0003t0001g0285 a0001c0003t0002g0319 |
3 | HG02886.hp1 NA18953.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.127-19804_127-1980 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837510 | |||||||
| chr12:124837510 | A | G | 120 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0067 others(117): Show |
121 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.127-19803T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837510 | |||||||
| chr12:124837510 | AAAAG | A | 6 | a0001c0001t0001g0039 a0001c0001t0004g0324 a0001c0001t0005g0043 others(3): Show |
6 | HG00438.hp1 HG02257.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-19807_127-1980 others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837510 | |||||||
| chr12:124837511 | A | G | 24 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0161 others(21): Show |
24 | HG01243.hp1 HG01256.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.127-19804T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837511 | |||||||
| chr12:124837512 | A | G | 55 | a0001c0001t0001g0072 a0001c0001t0001g0173 a0001c0001t0001g0174 others(52): Show |
55 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.127-19805T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837512 | |||||||
| chr12:124837513 | A | G | 58 | a0001c0001t0001g0072 a0001c0001t0001g0173 a0001c0001t0001g0174 others(55): Show |
58 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.127-19806T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837513 | |||||||
| chr12:124837515 | A | G | 27 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0152 others(24): Show |
27 | HG00438.hp1 HG00639.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.127-19808T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837515 | |||||||
| chr12:124837516 | A | G | 74 | a0001c0001t0001g0039 a0001c0001t0001g0072 a0001c0001t0001g0132 others(71): Show |
74 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.127-19809T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837516 | |||||||
| chr12:124837517 | A | G | 3 | a0001c0001t0008g0125 a0001c0003t0001g0285 a0001c0003t0002g0319 |
3 | HG02886.hp1 NA18953.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.127-19810T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837517 | |||||||
| chr12:124837517 | AAGAAAG | A | 13 | a0001c0001t0004g0121 a0001c0001t0016g0240 a0001c0002t0001g0143 others(10): Show |
13 | HG01243.hp1 HG01256.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-19816_127-1981 others(10): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837517 | |||||||
| chr12:124837518 | A | G | 24 | a0001c0001t0001g0019 a0001c0001t0001g0152 a0001c0001t0003g0020 others(21): Show |
24 | HG00639.hp1 HG01106.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.127-19811T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837518 | |||||||
| chr12:124837520 | A | G | 22 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0281 others(19): Show |
22 | HG00438.hp1 HG01884.hp1 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-19813T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837520 | |||||||
| chr12:124837521 | A | G | 3 | a0001c0001t0008g0125 a0001c0003t0001g0285 a0001c0003t0002g0319 |
3 | HG02886.hp1 NA18953.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.127-19814T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837521 | |||||||
| chr12:124837522 | A | G | 21 | a0001c0001t0001g0019 a0001c0001t0001g0152 a0001c0001t0003g0020 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.127-19815T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837522 | |||||||
| chr12:124837522 | AG | A | 55 | a0001c0001t0001g0072 a0001c0001t0001g0173 a0001c0001t0001g0174 others(52): Show |
55 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.127-19816delC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837522 | |||||||
| chr12:124837523 | G | A | 3 | a0001c0001t0008g0125 a0001c0003t0001g0285 a0001c0003t0002g0319 |
3 | HG02886.hp1 NA18953.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.127-19816C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837523 | |||||||
| chr12:124837526 | A | G | 21 | a0001c0001t0001g0019 a0001c0001t0001g0152 a0001c0001t0003g0020 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.127-19819T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837526 | |||||||
| chr12:124837527 | A | G | 22 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0281 others(19): Show |
22 | HG00438.hp1 HG01884.hp1 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-19820T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837527 | |||||||
| chr12:124837527 | AG | A | 21 | a0001c0001t0001g0019 a0001c0001t0001g0152 a0001c0001t0003g0020 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.127-19821delC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837527 | |||||||
| chr12:124837528 | GA | G | 69 | a0001c0001t0001g0072 a0001c0001t0001g0173 a0001c0001t0001g0174 others(66): Show |
69 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.127-19822delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837528 | |||||||
| chr12:124837529 | A | G | 22 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0281 others(19): Show |
22 | HG00438.hp1 HG01884.hp1 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-19822T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837529 | |||||||
| chr12:124837530 | A | G | 21 | a0001c0001t0001g0019 a0001c0001t0001g0152 a0001c0001t0003g0020 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.127-19823T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837530 | |||||||
| chr12:124837531 | A | G | 22 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0281 others(19): Show |
22 | HG00438.hp1 HG01884.hp1 HG02165.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-19824T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837531 | |||||||
| chr12:124837534 | G | GAAAGA | 4 | a0001c0001t0003g0170 a0001c0001t0003g0224 a0001c0001t0006g0225 others(1): Show |
4 | HG01891.hp2 HG02280.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-19832_127-1982 others(9): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837534 | |||||||
| chr12:124837534 | G | GAAAGAAA others(3): Show |
3 | a0001c0001t0003g0023 a0001c0001t0003g0183 a0001c0001t0003g0328 |
3 | HG02257.hp2 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.127-19837_127-1982 others(14): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837534 | |||||||
| chr12:124837534 | G | GAAAGAAA others(13): Show |
1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-19847_127-1982 others(24): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837534 | |||||||
| chr12:124837538 | GA | G | 59 | a0001c0001t0001g0092 a0001c0001t0001g0105 a0001c0001t0001g0144 others(56): Show |
60 | HG00280.hp2 HG00323.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.127-19832delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837538 | |||||||
| chr12:124837538 | GAAAAGA | G | 38 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0112 others(35): Show |
38 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.127-19837_127-1983 others(10): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837538 | |||||||
| chr12:124837538 | GAAAAGAA others(4): Show |
G | 7 | a0001c0001t0002g0244 a0001c0001t0002g0316 a0001c0002t0001g0097 others(4): Show |
7 | HG00544.hp2 HG02602.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-19842_127-1983 others(15): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837538 | |||||||
| chr12:124837538 | GAAAAGAA others(9): Show |
G | 2 | a0002c0006t0002g0017 a0002c0006t0005g0018 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.127-19847_127-1983 others(20): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837538 | |||||||
| chr12:124837539 | A | G | 71 | a0001c0001t0001g0072 a0001c0001t0001g0173 a0001c0001t0001g0174 others(68): Show |
71 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.127-19832T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837539 | |||||||
| chr12:124837541 | AAGAAAAG others(15): Show |
A | 3 | a0001c0005t0003g0354 a0001c0005t0003g0355 a0003c0009t0003g0123 |
3 | HG02572.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.127-19856_127-1983 others(26): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837541 | |||||||
| chr12:124837547 | A | G | 43 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0132 others(40): Show |
43 | HG00438.hp1 HG00639.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.127-19840T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837547 | |||||||
| chr12:124837548 | G | A | 71 | a0001c0001t0001g0072 a0001c0001t0001g0173 a0001c0001t0001g0174 others(68): Show |
71 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.127-19841C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837548 | |||||||
| chr12:124837549 | A | G | 71 | a0001c0001t0001g0072 a0001c0001t0001g0173 a0001c0001t0001g0174 others(68): Show |
71 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.127-19842T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837549 | |||||||
| chr12:124837552 | A | G | 43 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0132 others(40): Show |
43 | HG00438.hp1 HG00639.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.127-19845T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837552 | |||||||
| chr12:124837553 | G | A | 43 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0132 others(40): Show |
43 | HG00438.hp1 HG00639.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.127-19846C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837553 | |||||||
| chr12:124837556 | AAG | A | 47 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(44): Show |
47 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.127-19851_127-1985 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837556 | |||||||
| chr12:124837556 | AAGAAAAG | A | 23 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(20): Show |
23 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.127-19856_127-1985 others(11): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837556 | |||||||
| chr12:124837559 | A | AAAG | 3 | a0001c0001t0004g0324 a0001c0001t0006g0022 a0007c0014t0004g0033 |
3 | HG02896.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.127-19853_127-1985 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837559 | |||||||
| chr12:124837559 | A | G | 47 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(44): Show |
47 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.127-19852T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837559 | |||||||
| chr12:124837560 | A | AAG | 21 | a0001c0001t0001g0019 a0001c0001t0001g0152 a0001c0001t0003g0020 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.127-19854_127-1985 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837560 | |||||||
| chr12:124837561 | AAG | A | 16 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0281 others(13): Show |
16 | HG00438.hp1 HG02165.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.127-19856_127-1985 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837561 | |||||||
| chr12:124837563 | G | A | 21 | a0001c0001t0001g0019 a0001c0001t0001g0152 a0001c0001t0003g0020 others(18): Show |
21 | HG00639.hp1 HG01106.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.127-19856C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837563 | |||||||
| chr12:124837563 | GAAAAGAA others(24): Show |
G | 2 | a0001c0001t0006g0035 a0001c0002t0003g0075 |
2 | HG01069.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.127-19887_127-1985 others(35): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837563 | |||||||
| chr12:124837564 | A | G | 63 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0132 others(60): Show |
63 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.127-19857T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837564 | |||||||
| chr12:124837568 | GAAAAGAA others(19): Show |
G | 2 | a0001c0002t0003g0076 a0001c0002t0003g0077 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.127-19887_127-1986 others(30): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837568 | |||||||
| chr12:124837569 | A | G | 3 | a0001c0001t0008g0126 a0001c0001t0014g0127 a0001c0001t0017g0028 |
3 | HG01884.hp1 HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.127-19862T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837569 | |||||||
| chr12:124837571 | AAGAAAAG others(15): Show |
A | 35 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0162 others(32): Show |
35 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.127-19886_127-1986 others(26): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837571 | |||||||
| chr12:124837573 | GAAAAGAA others(14): Show |
G | 12 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0145 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-19887_127-1986 others(25): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837573 | |||||||
| chr12:124837578 | GAAAAGAA others(9): Show |
G | 20 | a0001c0001t0001g0050 a0001c0001t0001g0171 a0001c0001t0001g0185 others(17): Show |
20 | HG00408.hp2 HG01081.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.127-19887_127-1987 others(20): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837578 | |||||||
| chr12:124837583 | GAAAAGAA others(4): Show |
G | 47 | a0001c0001t0001g0094 a0001c0001t0001g0130 a0001c0001t0001g0193 others(44): Show |
47 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.127-19887_127-1987 others(15): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837583 | |||||||
| chr12:124837588 | GAAAAGA | G | 16 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0184 others(13): Show |
16 | HG00099.hp1 HG01081.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.127-19887_127-1988 others(10): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837588 | |||||||
| chr12:124837591 | AAG | A | 182 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(179): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.127-19886_127-1988 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837591 | |||||||
| chr12:124837593 | GA | G | 4 | a0001c0001t0001g0080 a0001c0002t0003g0138 a0001c0002t0003g0139 others(1): Show |
4 | HG00323.hp2 HG03927.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-19887delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837593 | |||||||
| chr12:124837594 | A | AAAAGAAA others(7): Show |
2 | a0001c0001t0003g0267 a0001c0003t0004g0321 |
2 | NA18963.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.127-19888_127-1988 others(18): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837594 | |||||||
| chr12:124837594 | A | AAAAGAAA others(12): Show |
2 | a0001c0002t0001g0081 a0001c0002t0001g0269 |
2 | HG00140.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.127-19888_127-1988 others(23): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837594 | |||||||
| chr12:124837594 | A | AAAAGAAA others(17): Show |
2 | a0001c0003t0002g0263 a0001c0003t0002g0280 |
2 | NA18992.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.127-19888_127-1988 others(28): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837594 | |||||||
| chr12:124837594 | A | AAAAGAAA others(22): Show |
1 | a0001c0003t0002g0268 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.127-19888_127-1988 others(33): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837594 | |||||||
| chr12:124837594 | A | AAAAGAAA others(27): Show |
1 | a0001c0002t0001g0254 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.127-19888_127-1988 others(38): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837594 | |||||||
| chr12:124837594 | A | AAAG | 6 | a0001c0001t0004g0324 a0001c0001t0008g0125 a0001c0002t0001g0085 others(3): Show |
6 | HG01099.hp2 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-19888_127-1988 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837594 | |||||||
| chr12:124837594 | A | G | 217 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(214): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.127-19887T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837594 | |||||||
| chr12:124837604 | C | T | 6 | a0001c0001t0003g0232 a0001c0001t0004g0324 a0001c0001t0006g0022 others(3): Show |
6 | HG02559.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-19897G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837604 | |||||||
| chr12:124837624 | C | A | 23 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0165 others(20): Show |
23 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.127-19917G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837624 | |||||||
| chr12:124837624 | C | T | 1 | a0001c0003t0002g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.127-19917G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837624 | |||||||
| chr12:124837736 | A | C | 23 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0165 others(20): Show |
23 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.127-20029T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837736 | |||||||
| chr12:124837742 | TA | T | 248 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0040 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.127-20036delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837742 | |||||||
| chr12:124837777 | G | A | 1 | a0001c0001t0017g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127-20070C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124837777 | |||||||
| chr12:124838068 | T | C | 1 | a0001c0001t0003g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.127-20361A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838068 | |||||||
| chr12:124838281 | C | T | 77 | a0001c0001t0001g0019 a0001c0001t0001g0072 a0001c0001t0001g0270 others(74): Show |
77 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(74): Show |
intron_variant | MODIFIER | c.127-20574G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838281 | |||||||
| chr12:124838449 | G | C | 175 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0050 others(172): Show |
175 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.127-20742C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838449 | |||||||
| chr12:124838504 | C | A | 1 | a0001c0002t0003g0091 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.127-20797G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838504 | |||||||
| chr12:124838591 | G | A | 1 | a0001c0001t0004g0121 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.127-20884C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838591 | |||||||
| chr12:124838644 | G | A | 7 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0003g0161 others(4): Show |
7 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-20937C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838644 | |||||||
| chr12:124838664 | A | G | 7 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0003g0161 others(4): Show |
7 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-20957T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838664 | |||||||
| chr12:124838694 | G | A | 91 | a0001c0001t0001g0034 a0001c0001t0001g0050 a0001c0001t0001g0052 others(88): Show |
91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.127-20987C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838694 | |||||||
| chr12:124838717 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.127-21010T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838717 | |||||||
| chr12:124838775 | C | CT | 116 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0072 others(113): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.127-21069dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838775 | |||||||
| chr12:124838775 | C | CTT | 143 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0050 others(140): Show |
143 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.127-21070_127-2106 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838775 | |||||||
| chr12:124838775 | C | CTTT | 20 | a0001c0001t0001g0092 a0001c0001t0001g0159 a0001c0001t0001g0241 others(17): Show |
20 | HG00673.hp2 HG01358.hp1 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.127-21071_127-2106 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838775 | |||||||
| chr12:124838775 | C | CTTTT | 6 | a0001c0001t0008g0126 a0001c0001t0014g0127 a0001c0001t0017g0028 others(3): Show |
6 | HG00735.hp2 HG01515.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-21072_127-2106 others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838775 | |||||||
| chr12:124838775 | CTT | C | 10 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0003g0161 others(7): Show |
10 | HG02559.hp2 HG02572.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-21070_127-2106 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838775 | |||||||
| chr12:124838775 | CTTT | C | 6 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0004g0324 others(3): Show |
6 | HG02615.hp1 HG02896.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-21071_127-2106 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838775 | |||||||
| chr12:124838788 | T | C | 19 | a0001c0001t0003g0165 a0001c0001t0004g0121 a0001c0001t0016g0240 others(16): Show |
19 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.127-21081A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838788 | |||||||
| chr12:124838808 | G | C | 17 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0025 others(14): Show |
17 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.127-21101C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838808 | |||||||
| chr12:124838875 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.127-21168T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838875 | |||||||
| chr12:124838894 | C | A | 6 | a0001c0001t0003g0232 a0001c0001t0004g0324 a0001c0001t0006g0022 others(3): Show |
6 | HG02559.hp2 HG02572.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-21187G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838894 | |||||||
| chr12:124838920 | G | A | 1 | a0001c0002t0003g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.127-21213C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838920 | |||||||
| chr12:124838921 | C | A | 1 | a0001c0001t0001g0206 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.127-21214G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838921 | |||||||
| chr12:124838999 | T | C | 1 | a0001c0001t0002g0305 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.127-21292A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124838999 | |||||||
| chr12:124839047 | A | G | 14 | a0001c0001t0001g0186 a0001c0001t0001g0198 a0001c0001t0001g0206 others(11): Show |
14 | HG01069.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-21340T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839047 | |||||||
| chr12:124839065 | A | G | 22 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0025 others(19): Show |
22 | HG01361.hp1 HG02145.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-21358T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839065 | |||||||
| chr12:124839070 | C | G | 6 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0004g0026 others(3): Show |
6 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-21363G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839070 | |||||||
| chr12:124839072 | G | T | 1 | a0001c0001t0008g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.127-21365C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839072 | |||||||
| chr12:124839317 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0005g0255 |
2 | HG03491.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.127-21610G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839317 | |||||||
| chr12:124839320 | T | C | 6 | a0001c0001t0001g0034 a0001c0001t0006g0031 a0001c0001t0006g0035 others(3): Show |
6 | HG02630.hp1 HG02970.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-21613A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839320 | |||||||
| chr12:124839416 | A | C | 50 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(47): Show |
50 | HG00544.hp2 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.127-21709T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839416 | |||||||
| chr12:124839447 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.127-21740G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839447 | |||||||
| chr12:124839469 | T | A | 1 | a0001c0001t0002g0305 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.127-21762A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839469 | |||||||
| chr12:124839514 | G | C | 1 | a0001c0002t0001g0254 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.127-21807C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839514 | |||||||
| chr12:124839580 | C | T | 1 | a0004c0011t0002g0210 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.127-21873G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839580 | |||||||
| chr12:124839644 | T | TCCCAACA others(34): Show |
64 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0080 others(61): Show |
65 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.127-21938_127-2193 others(45): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(362): Show |
1 | a0001c0002t0001g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.127-21938_127-2193 others(373): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(157): Show |
1 | a0001c0002t0001g0189 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.127-21938_127-2193 others(168): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(813): Show |
1 | a0001c0003t0002g0268 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.127-21938_127-2193 others(824): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(75): Show |
66 | a0001c0001t0001g0039 a0001c0001t0001g0050 a0001c0001t0001g0052 others(63): Show |
66 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.127-21938_127-2193 others(86): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(116): Show |
5 | a0001c0001t0004g0026 a0001c0001t0012g0060 a0001c0002t0001g0332 others(2): Show |
5 | HG02451.hp1 HG02723.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-21938_127-2193 others(127): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(157): Show |
3 | a0001c0001t0003g0029 a0001c0001t0017g0030 a0001c0004t0015g0059 |
3 | HG02109.hp1 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.127-21938_127-2193 others(168): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(280): Show |
1 | a0002c0006t0004g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-21938_127-2193 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(403): Show |
1 | a0001c0003t0002g0263 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.127-21938_127-2193 others(414): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(649): Show |
1 | a0001c0003t0002g0280 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.127-21938_127-2193 others(660): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(116): Show |
2 | a0001c0002t0007g0058 a0001c0005t0001g0350 |
2 | HG01993.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.127-21938_127-2193 others(127): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(280): Show |
1 | a0001c0002t0003g0164 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.127-21938_127-2193 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(485): Show |
1 | a0001c0007t0001g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.127-21938_127-2193 others(496): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(403): Show |
1 | a0001c0007t0005g0191 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.127-21938_127-2193 others(414): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(280): Show |
1 | a0001c0002t0001g0081 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.127-21938_127-2193 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(731): Show |
4 | a0001c0001t0003g0267 a0001c0002t0001g0254 a0001c0002t0002g0320 others(1): Show |
4 | HG00621.hp1 NA18954.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-21938_127-2193 others(742): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(731): Show |
1 | a0001c0002t0001g0269 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.127-21938_127-2193 others(742): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(772): Show |
1 | a0001c0001t0003g0266 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.127-21938_127-2193 others(783): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(321): Show |
1 | a0001c0003t0002g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.127-21938_127-2193 others(332): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(75): Show |
7 | a0001c0001t0001g0209 a0001c0001t0005g0045 a0001c0002t0001g0333 others(4): Show |
7 | HG01256.hp2 HG01258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-21938_127-2193 others(86): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(157): Show |
1 | a0001c0002t0003g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.127-21938_127-2193 others(168): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(239): Show |
1 | a0001c0001t0003g0114 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.127-21938_127-2193 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(280): Show |
1 | a0001c0001t0006g0225 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.127-21938_127-2193 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(567): Show |
1 | a0001c0001t0008g0233 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.127-21938_127-2193 others(578): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(567): Show |
1 | a0001c0001t0003g0232 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.127-21938_127-2193 others(578): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(444): Show |
1 | a0007c0014t0004g0033 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.127-21938_127-2193 others(455): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(567): Show |
1 | a0001c0001t0006g0022 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-21938_127-2193 others(578): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(567): Show |
1 | a0002c0006t0006g0010 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127-21938_127-2193 others(578): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | T | TCCCAACA others(813): Show |
1 | a0001c0001t0003g0161 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.127-21938_127-2193 others(824): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | TCCCAACG others(34): Show |
T | 2 | a0001c0001t0008g0331 a0001c0013t0016g0334 |
2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.127-21978_127-2193 others(45): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | TCCCAACG others(116): Show |
T | 3 | a0001c0001t0001g0223 a0001c0001t0003g0226 a0001c0004t0014g0190 |
3 | HG02559.hp1 HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.127-22060_127-2193 others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | TCCCAACG others(280): Show |
T | 1 | a0001c0001t0003g0183 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.127-22224_127-2193 others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839644 | TCCCAACG others(321): Show |
T | 2 | a0001c0001t0003g0023 a0001c0001t0003g0328 |
2 | HG02257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.127-22265_127-2193 others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839644 | |||||||
| chr12:124839651 | G | A | 151 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0111 others(148): Show |
151 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.127-21944C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839651 | |||||||
| chr12:124839651 | G | GGCACACA others(75): Show |
1 | a0001c0001t0004g0324 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.127-21945_127-2194 others(86): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839651 | |||||||
| chr12:124839660 | G | GGGCCCCC others(157): Show |
1 | a0001c0003t0002g0167 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.127-21954_127-2195 others(168): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839660 | |||||||
| chr12:124839675 | C | CACACCCT others(157): Show |
1 | a0001c0003t0002g0300 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.127-21969_127-2196 others(168): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839675 | |||||||
| chr12:124839675 | C | CACACCCT others(116): Show |
8 | a0001c0001t0001g0072 a0001c0001t0001g0287 a0001c0001t0001g0288 others(5): Show |
8 | HG01099.hp1 HG01123.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-21969_127-2196 others(127): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839675 | |||||||
| chr12:124839675 | C | CGCACCCT others(34): Show |
4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0025g0180 others(1): Show |
4 | HG02615.hp1 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-21969_127-2196 others(45): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839675 | |||||||
| chr12:124839675 | C | CGCACCCT others(205): Show |
1 | a0001c0001t0002g0305 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.127-21969_127-2196 others(216): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839675 | |||||||
| chr12:124839675 | C | T | 1 | a0001c0001t0008g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-21968G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839675 | |||||||
| chr12:124839676 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.127-21969C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839676 | |||||||
| chr12:124839692 | G | A | 94 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0146 others(91): Show |
94 | HG00280.hp1 HG00621.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.127-21985C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839692 | |||||||
| chr12:124839692 | G | GGCACACA others(116): Show |
2 | a0001c0002t0001g0304 a0001c0003t0013g0339 |
2 | NA19065.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.127-21986_127-2198 others(127): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839692 | |||||||
| chr12:124839692 | G | GGCACACA others(280): Show |
2 | a0001c0001t0004g0297 a0001c0007t0010g0156 |
2 | HG02135.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.127-21986_127-2198 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839692 | |||||||
| chr12:124839692 | G | GGCACACA others(116): Show |
14 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0002g0115 others(11): Show |
14 | HG00609.hp2 HG02056.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-21986_127-2198 others(127): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839692 | |||||||
| chr12:124839692 | G | GGCACACA others(34): Show |
8 | a0001c0001t0001g0152 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG00738.hp1 HG01071.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-21986_127-2198 others(45): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839692 | |||||||
| chr12:124839717 | G | GCACACTC others(116): Show |
1 | a0001c0002t0001g0306 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.127-22011_127-2201 others(127): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839717 | |||||||
| chr12:124839717 | G | GCACACTC others(731): Show |
1 | a0001c0002t0001g0312 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.127-22011_127-2201 others(742): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839717 | |||||||
| chr12:124839721 | C | A | 8 | a0001c0001t0001g0279 a0001c0002t0001g0168 a0001c0003t0001g0295 others(5): Show |
8 | HG01928.hp2 HG02273.hp2 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-22014G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839721 | |||||||
| chr12:124839733 | G | A | 42 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0173 others(39): Show |
42 | HG00609.hp2 HG00735.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.127-22026C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839733 | |||||||
| chr12:124839733 | G | GGCACACA others(239): Show |
2 | a0001c0001t0004g0121 a0001c0005t0003g0355 |
2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.127-22027_127-2202 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839733 | |||||||
| chr12:124839733 | G | GGCACACA others(280): Show |
3 | a0001c0001t0016g0240 a0001c0005t0003g0349 a0001c0005t0004g0347 |
3 | HG01243.hp1 HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.127-22027_127-2202 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839733 | |||||||
| chr12:124839733 | G | GGCACACA others(116): Show |
1 | a0001c0001t0001g0279 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.127-22027_127-2202 others(127): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839733 | |||||||
| chr12:124839751 | T | TTTCTCCG others(33): Show |
3 | a0001c0001t0001g0105 a0001c0002t0001g0101 a0001c0002t0001g0177 |
3 | HG00639.hp2 HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.127-22084_127-2204 others(44): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839751 | |||||||
| chr12:124839755 | T | C | 1 | a0001c0001t0012g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.127-22048A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839755 | |||||||
| chr12:124839758 | G | A | 29 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(26): Show |
29 | HG00609.hp2 HG01099.hp1 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.127-22051C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839758 | |||||||
| chr12:124839758 | G | GCACACTC others(157): Show |
1 | a0001c0003t0010g0283 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.127-22052_127-2205 others(168): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839758 | |||||||
| chr12:124839758 | G | GCACACTC others(157): Show |
7 | a0001c0002t0001g0168 a0001c0003t0001g0295 a0001c0003t0001g0296 others(4): Show |
7 | HG01928.hp2 NA18953.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-22052_127-2205 others(168): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839758 | |||||||
| chr12:124839759 | C | CACCCTCA others(280): Show |
1 | a0001c0003t0002g0275 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.127-22053_127-2205 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839759 | |||||||
| chr12:124839759 | C | CACCCTCA others(403): Show |
1 | a0001c0001t0001g0301 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.127-22053_127-2205 others(414): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839759 | |||||||
| chr12:124839759 | C | CACCCTCA others(403): Show |
1 | a0001c0002t0001g0143 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.127-22053_127-2205 others(414): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839759 | |||||||
| chr12:124839759 | C | CACCCTCA others(444): Show |
2 | a0001c0001t0002g0128 a0001c0001t0005g0084 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.127-22053_127-2205 others(455): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839759 | |||||||
| chr12:124839759 | C | T | 1 | a0001c0002t0001g0312 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.127-22052G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839759 | |||||||
| chr12:124839761 | C | T | 1 | a0001c0001t0008g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.127-22054G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839761 | |||||||
| chr12:124839762 | C | A | 6 | a0001c0003t0001g0307 a0001c0003t0002g0182 a0001c0003t0002g0188 others(3): Show |
6 | HG00408.hp1 HG02071.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-22055G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839762 | |||||||
| chr12:124839766 | A | ACCCCAAC others(239): Show |
2 | a0001c0001t0005g0045 a0001c0004t0015g0044 |
2 | HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.127-22060_127-2205 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839766 | |||||||
| chr12:124839774 | G | A | 47 | a0001c0001t0001g0072 a0001c0001t0001g0198 a0001c0001t0001g0270 others(44): Show |
47 | HG00408.hp1 HG00735.hp1 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.127-22067C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839774 | |||||||
| chr12:124839782 | T | C | 1 | a0001c0001t0008g0046 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.127-22075A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839782 | |||||||
| chr12:124839796 | T | C | 2 | a0001c0001t0012g0062 a0001c0001t0019g0061 |
2 | HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.127-22089A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839796 | |||||||
| chr12:124839800 | C | CACACTCA others(198): Show |
1 | a0001c0001t0002g0292 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.127-22094_127-2209 others(209): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839800 | |||||||
| chr12:124839800 | C | CACACTCA others(239): Show |
1 | a0001c0003t0001g0285 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.127-22094_127-2209 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839800 | |||||||
| chr12:124839800 | C | CACACTCA others(198): Show |
1 | a0001c0003t0001g0307 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.127-22094_127-2209 others(209): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839800 | |||||||
| chr12:124839800 | C | CACCCTCA others(239): Show |
1 | a0001c0003t0013g0276 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.127-22094_127-2209 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839800 | |||||||
| chr12:124839800 | C | T | 38 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(35): Show |
38 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.127-22093G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839800 | |||||||
| chr12:124839802 | C | T | 1 | a0001c0001t0008g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.127-22095G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839802 | |||||||
| chr12:124839803 | C | A | 3 | a0001c0001t0003g0029 a0001c0002t0001g0227 a0002c0006t0004g0012 |
3 | HG02922.hp2 HG02965.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.127-22096G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839803 | |||||||
| chr12:124839815 | G | A | 10 | a0001c0001t0003g0117 a0001c0001t0003g0165 a0001c0001t0006g0118 others(7): Show |
10 | HG00408.hp1 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-22108C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839815 | |||||||
| chr12:124839815 | G | GGCACACA others(321): Show |
5 | a0001c0005t0003g0352 a0001c0005t0003g0354 a0001c0005t0004g0346 others(2): Show |
5 | HG02486.hp1 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-22109_127-2210 others(332): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839815 | |||||||
| chr12:124839828 | C | A | 1 | a0001c0001t0008g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.127-22121G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839828 | |||||||
| chr12:124839832 | ATTTCTCC others(35): Show |
A | 1 | a0001c0001t0022g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.127-22167_127-2212 others(46): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839832 | |||||||
| chr12:124839844 | C | A | 4 | a0001c0001t0001g0130 a0001c0001t0003g0038 a0001c0001t0003g0239 others(1): Show |
4 | HG01361.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-22137G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839844 | |||||||
| chr12:124839848 | A | ACCCCAAC others(75): Show |
2 | a0001c0001t0001g0176 a0001c0002t0001g0158 |
2 | HG00738.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.127-22142_127-2214 others(86): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839848 | |||||||
| chr12:124839856 | G | A | 7 | a0001c0001t0001g0130 a0001c0001t0003g0165 a0001c0001t0016g0240 others(4): Show |
7 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-22149C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839856 | |||||||
| chr12:124839884 | C | T | 9 | a0001c0001t0003g0038 a0001c0001t0003g0239 a0001c0001t0004g0026 others(6): Show |
9 | HG01361.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-22177G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839884 | |||||||
| chr12:124839889 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0018g0071 |
2 | HG01071.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.127-22182T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839889 | |||||||
| chr12:124839897 | G | A | 4 | a0001c0001t0001g0130 a0001c0004t0015g0059 a0001c0005t0001g0350 others(1): Show |
4 | HG02109.hp2 NA18906.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-22190C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839897 | |||||||
| chr12:124839925 | C | CCCTCACC others(280): Show |
1 | a0001c0005t0003g0351 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.127-22219_127-2221 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839925 | |||||||
| chr12:124839925 | C | CCCTCACC others(116): Show |
1 | a0001c0001t0012g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.127-22219_127-2221 others(127): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839925 | |||||||
| chr12:124839925 | C | T | 8 | a0001c0001t0004g0121 a0001c0001t0016g0240 a0001c0002t0001g0163 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-22218G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839925 | |||||||
| chr12:124839926 | C | A | 28 | a0001c0001t0001g0301 a0001c0001t0002g0128 a0001c0001t0003g0266 others(25): Show |
28 | HG00621.hp1 HG01257.hp1 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.127-22219G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839926 | |||||||
| chr12:124839926 | C | CCTCGCCC others(321): Show |
1 | a0001c0001t0005g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.127-22220_127-2221 others(332): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839926 | |||||||
| chr12:124839926 | C | G | 3 | a0001c0001t0003g0029 a0001c0001t0008g0027 a0002c0006t0004g0012 |
3 | HG02723.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.127-22219G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839926 | |||||||
| chr12:124839930 | A | G | 7 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-22223T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839930 | |||||||
| chr12:124839938 | G | A | 3 | a0001c0017t0005g0341 a0002c0006t0006g0011 a0003c0009t0003g0123 |
3 | HG02109.hp2 HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.127-22231C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839938 | |||||||
| chr12:124839966 | C | CCCTCGCC others(198): Show |
2 | a0001c0001t0001g0152 a0001c0002t0003g0153 |
2 | HG01106.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.127-22260_127-2225 others(209): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839966 | |||||||
| chr12:124839966 | C | CCCTCGCC others(321): Show |
1 | a0001c0001t0008g0046 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.127-22260_127-2225 others(332): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839966 | |||||||
| chr12:124839966 | C | T | 16 | a0001c0001t0001g0184 a0001c0001t0001g0241 a0001c0001t0003g0161 others(13): Show |
16 | HG02145.hp1 HG02559.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.127-22259G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839966 | |||||||
| chr12:124839967 | C | A | 54 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(51): Show |
54 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.127-22260G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839967 | |||||||
| chr12:124839967 | C | CCTCACCC others(197): Show |
1 | a0001c0003t0002g0095 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.127-22261_127-2226 others(208): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839967 | |||||||
| chr12:124839971 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.127-22264T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839971 | |||||||
| chr12:124839983 | C | T | 1 | a0001c0001t0022g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.127-22276G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124839983 | |||||||
| chr12:124840007 | C | CACTCACC others(198): Show |
2 | a0001c0001t0001g0171 a0001c0003t0002g0069 |
2 | HG01081.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.127-22301_127-2230 others(209): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840007 | |||||||
| chr12:124840007 | C | CACTCACC others(116): Show |
1 | a0001c0002t0001g0085 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.127-22301_127-2230 others(127): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840007 | |||||||
| chr12:124840007 | C | CACTCACC others(34): Show |
1 | a0001c0002t0001g0220 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.127-22301_127-2230 others(45): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840007 | |||||||
| chr12:124840007 | C | CACTCACC others(75): Show |
3 | a0001c0001t0001g0176 a0001c0001t0008g0125 a0001c0002t0001g0158 |
3 | HG00738.hp1 HG01256.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.127-22301_127-2230 others(86): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840007 | |||||||
| chr12:124840007 | C | CACTCACC others(157): Show |
9 | a0001c0001t0001g0184 a0001c0001t0001g0241 a0001c0001t0006g0024 others(6): Show |
9 | HG01243.hp2 HG02615.hp2 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.127-22301_127-2230 others(168): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840007 | |||||||
| chr12:124840007 | C | CCCTCACC others(157): Show |
2 | a0001c0001t0001g0174 a0001c0001t0018g0071 |
2 | HG01071.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.127-22301_127-2230 others(168): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840007 | |||||||
| chr12:124840007 | C | T | 82 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(79): Show |
82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.127-22300G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840007 | |||||||
| chr12:124840008 | C | A | 1 | a0002c0006t0004g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-22301G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840008 | |||||||
| chr12:124840020 | G | A | 17 | a0001c0001t0001g0301 a0001c0001t0002g0128 a0001c0001t0003g0161 others(14): Show |
17 | HG01257.hp1 HG01258.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.127-22313C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840020 | |||||||
| chr12:124840024 | C | CACATGGG others(444): Show |
1 | a0003c0009t0003g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.127-22318_127-2231 others(455): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(239): Show |
2 | a0001c0001t0003g0074 a0001c0002t0003g0075 |
2 | HG01069.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.127-22318_127-2231 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(157): Show |
5 | a0001c0001t0001g0040 a0001c0001t0001g0105 a0001c0002t0001g0101 others(2): Show |
5 | HG00738.hp2 HG01168.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(168): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(116): Show |
2 | a0001c0001t0004g0324 a0007c0014t0004g0033 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.127-22318_127-2231 others(127): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(199): Show |
1 | a0001c0003t0002g0167 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.127-22318_127-2231 others(210): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(198): Show |
47 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(44): Show |
47 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(209): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(116): Show |
4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0017g0030 others(1): Show |
4 | HG02109.hp1 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(127): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(239): Show |
1 | a0002c0006t0006g0011 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.127-22318_127-2231 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(198): Show |
4 | a0001c0001t0002g0096 a0001c0002t0001g0177 a0001c0003t0002g0103 others(1): Show |
4 | HG00639.hp2 NA18983.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(209): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(239): Show |
2 | a0001c0001t0001g0186 a0001c0001t0001g0206 |
2 | HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.127-22318_127-2231 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(157): Show |
5 | a0001c0001t0001g0039 a0001c0001t0001g0175 a0001c0002t0001g0151 others(2): Show |
5 | HG02647.hp2 HG02683.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(168): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(444): Show |
1 | a0001c0001t0002g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.127-22318_127-2231 others(455): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(567): Show |
1 | a0001c0001t0003g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.127-22318_127-2231 others(578): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(280): Show |
1 | a0001c0017t0005g0341 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.127-22318_127-2231 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(239): Show |
38 | a0001c0001t0001g0067 a0001c0001t0001g0094 a0001c0001t0001g0112 others(35): Show |
39 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(36): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(772): Show |
1 | a0001c0002t0003g0070 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.127-22318_127-2231 others(783): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(198): Show |
4 | a0001c0001t0001g0173 a0001c0001t0003g0038 a0001c0001t0003g0239 others(1): Show |
4 | HG01069.hp1 HG01361.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(209): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(280): Show |
4 | a0001c0001t0003g0246 a0001c0002t0005g0336 a0001c0002t0005g0337 others(1): Show |
4 | HG02071.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(239): Show |
1 | a0001c0003t0002g0263 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.127-22318_127-2231 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(239): Show |
8 | a0001c0001t0001g0132 a0001c0001t0003g0140 a0001c0001t0003g0142 others(5): Show |
8 | HG02055.hp1 HG03041.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(321): Show |
1 | a0001c0003t0001g0098 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.127-22318_127-2231 others(332): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(280): Show |
6 | a0001c0001t0001g0281 a0001c0001t0025g0180 a0001c0002t0001g0133 others(3): Show |
6 | HG00438.hp1 HG02615.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(895): Show |
1 | a0001c0001t0003g0294 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.127-22318_127-2231 others(906): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(403): Show |
2 | a0001c0004t0002g0238 a0001c0004t0011g0119 |
2 | HG00673.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.127-22318_127-2231 others(414): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(403): Show |
2 | a0001c0003t0001g0262 a0001c0007t0003g0135 |
2 | HG02165.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.127-22318_127-2231 others(414): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(444): Show |
8 | a0001c0001t0001g0146 a0001c0001t0001g0162 a0001c0001t0003g0117 others(5): Show |
8 | HG01175.hp1 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(455): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(444): Show |
1 | a0001c0001t0017g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.127-22318_127-2231 others(455): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(485): Show |
5 | a0001c0001t0001g0092 a0001c0001t0004g0048 a0002c0006t0003g0008 others(2): Show |
5 | HG00735.hp2 HG01515.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(496): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(485): Show |
2 | a0001c0001t0008g0126 a0001c0001t0014g0127 |
2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.127-22318_127-2231 others(496): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(526): Show |
8 | a0001c0001t0001g0159 a0001c0001t0001g0242 a0001c0001t0001g0326 others(5): Show |
8 | HG01358.hp1 HG02040.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(537): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(567): Show |
6 | a0001c0002t0001g0236 a0001c0002t0001g0314 a0001c0003t0002g0129 others(3): Show |
6 | NA18948.hp2 NA18963.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(578): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(649): Show |
1 | a0001c0002t0001g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.127-22318_127-2231 others(660): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(690): Show |
1 | a0001c0001t0002g0234 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.127-22318_127-2231 others(701): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(690): Show |
1 | a0001c0001t0003g0260 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.127-22318_127-2231 others(701): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(567): Show |
1 | a0001c0004t0003g0203 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.127-22318_127-2231 others(578): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(485): Show |
6 | a0001c0001t0001g0130 a0001c0001t0001g0198 a0002c0006t0001g0003 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(496): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(444): Show |
10 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0002t0001g0227 others(7): Show |
10 | HG00280.hp1 HG01433.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(455): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(403): Show |
10 | a0001c0001t0001g0111 a0001c0001t0001g0185 a0001c0001t0001g0258 others(7): Show |
10 | HG00099.hp1 HG00408.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(414): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(444): Show |
1 | a0001c0001t0003g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.127-22318_127-2231 others(455): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(239): Show |
2 | a0001c0002t0003g0076 a0001c0002t0003g0077 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.127-22318_127-2231 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(239): Show |
1 | a0001c0007t0001g0063 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.127-22318_127-2231 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(198): Show |
1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.127-22318_127-2231 others(209): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(75): Show |
1 | a0002c0006t0004g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.127-22318_127-2231 others(86): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(198): Show |
2 | a0001c0004t0015g0059 a0001c0005t0001g0350 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.127-22318_127-2231 others(209): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(280): Show |
6 | a0001c0001t0001g0034 a0001c0001t0001g0202 a0001c0001t0006g0031 others(3): Show |
6 | HG02630.hp1 HG03471.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(321): Show |
1 | a0001c0001t0011g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.127-22318_127-2231 others(332): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(280): Show |
1 | a0001c0004t0001g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.127-22318_127-2231 others(291): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(157): Show |
1 | a0001c0001t0004g0026 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.127-22318_127-2231 others(168): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(34): Show |
53 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(50): Show |
53 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(45): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(239): Show |
7 | a0001c0001t0001g0080 a0001c0001t0001g0209 a0001c0001t0002g0221 others(4): Show |
7 | HG00323.hp2 HG01943.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.127-22318_127-2231 others(250): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(116): Show |
1 | a0001c0001t0012g0060 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.127-22318_127-2231 others(127): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | CACATGGG others(34): Show |
1 | a0001c0002t0001g0081 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.127-22318_127-2231 others(45): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840024 | C | T | 49 | a0001c0001t0001g0152 a0001c0001t0001g0171 a0001c0001t0001g0174 others(46): Show |
49 | HG00621.hp1 HG00639.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.127-22317G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840024 | |||||||
| chr12:124840148 | C | T | 52 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(49): Show |
52 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.127-22441G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840148 | |||||||
| chr12:124840185 | A | AT | 16 | a0001c0001t0001g0019 a0001c0001t0001g0152 a0001c0001t0001g0173 others(13): Show |
16 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.127-22479dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840185 | |||||||
| chr12:124840185 | AT | A | 24 | a0001c0001t0003g0165 a0001c0001t0003g0260 a0001c0001t0004g0121 others(21): Show |
24 | HG01243.hp1 HG01891.hp1 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.127-22479delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840185 | |||||||
| chr12:124840241 | T | G | 113 | a0001c0001t0001g0072 a0001c0001t0001g0092 a0001c0001t0001g0146 others(110): Show |
113 | HG00609.hp2 HG00621.hp2 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.127-22534A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840241 | |||||||
| chr12:124840252 | C | A | 12 | a0001c0001t0001g0152 a0001c0001t0001g0173 a0001c0001t0001g0174 others(9): Show |
12 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.127-22545G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840252 | |||||||
| chr12:124840269 | G | T | 37 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0159 others(34): Show |
37 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.127-22562C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840269 | |||||||
| chr12:124840270 | T | C | 37 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0159 others(34): Show |
37 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.127-22563A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840270 | |||||||
| chr12:124840275 | A | G | 37 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0159 others(34): Show |
37 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.127-22568T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840275 | |||||||
| chr12:124840277 | G | A | 37 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0159 others(34): Show |
37 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.127-22570C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840277 | |||||||
| chr12:124840281 | C | T | 37 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0159 others(34): Show |
37 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.127-22574G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840281 | |||||||
| chr12:124840284 | C | T | 37 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0159 others(34): Show |
37 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.127-22577G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840284 | |||||||
| chr12:124840322 | C | T | 1 | a0001c0002t0021g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.127-22615G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840322 | |||||||
| chr12:124840326 | T | C | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.127-22619A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840326 | |||||||
| chr12:124840434 | C | T | 19 | a0001c0001t0001g0111 a0001c0001t0001g0185 a0001c0001t0001g0198 others(16): Show |
19 | HG00099.hp1 HG00280.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.127-22727G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840434 | |||||||
| chr12:124840464 | C | G | 15 | a0001c0001t0001g0152 a0001c0001t0001g0173 a0001c0001t0001g0174 others(12): Show |
15 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.127-22757G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840464 | |||||||
| chr12:124840476 | G | T | 3 | a0001c0001t0003g0023 a0001c0001t0003g0183 a0001c0001t0003g0328 |
3 | HG02257.hp2 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.127-22769C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840476 | |||||||
| chr12:124840626 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0025g0180 others(1): Show |
4 | HG02615.hp1 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-22919C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840626 | |||||||
| chr12:124840713 | AC | A | 3 | a0001c0001t0008g0126 a0001c0001t0014g0127 a0001c0001t0017g0028 |
3 | HG01884.hp1 HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.126+22881delG | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840713 | |||||||
| chr12:124840785 | A | AC | 58 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(55): Show |
58 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.126+22809dupG | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840785 | |||||||
| chr12:124840819 | G | A | 6 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0004g0026 others(3): Show |
6 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+22776C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840819 | |||||||
| chr12:124840837 | G | A | 76 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(73): Show |
76 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(73): Show |
intron_variant | MODIFIER | c.126+22758C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840837 | |||||||
| chr12:124840975 | C | A | 36 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0159 others(33): Show |
36 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.126+22620G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840975 | |||||||
| chr12:124840986 | T | C | 51 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(48): Show |
51 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.126+22609A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124840986 | |||||||
| chr12:124841005 | C | T | 8 | a0001c0001t0001g0152 a0001c0001t0018g0071 a0001c0002t0001g0151 others(5): Show |
8 | HG01106.hp2 HG01123.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+22590G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841005 | |||||||
| chr12:124841098 | G | A | 6 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0004g0026 others(3): Show |
6 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+22497C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841098 | |||||||
| chr12:124841099 | C | T | 2 | a0001c0001t0001g0206 a0001c0002t0001g0205 |
2 | HG04184.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.126+22496G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841099 | |||||||
| chr12:124841126 | C | G | 18 | a0001c0001t0003g0165 a0001c0001t0004g0121 a0001c0001t0016g0240 others(15): Show |
18 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.126+22469G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841126 | |||||||
| chr12:124841232 | C | T | 26 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0132 others(23): Show |
26 | HG00438.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.126+22363G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841232 | |||||||
| chr12:124841244 | C | T | 69 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(66): Show |
69 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.126+22351G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841244 | |||||||
| chr12:124841262 | C | T | 2 | a0001c0001t0006g0041 a0001c0020t0003g0343 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.126+22333G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841262 | |||||||
| chr12:124841270 | G | A | 6 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0004g0026 others(3): Show |
6 | HG02723.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.126+22325C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841270 | |||||||
| chr12:124841304 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.126+22291C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841304 | |||||||
| chr12:124841308 | C | T | 1 | a0001c0001t0017g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.126+22287G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841308 | |||||||
| chr12:124841320 | G | A | 3 | a0001c0001t0001g0193 a0001c0003t0002g0160 a0001c0003t0002g0214 |
3 | NA18975.hp2 NA18998.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.126+22275C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841320 | |||||||
| chr12:124841329 | G | A | 58 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(55): Show |
58 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.126+22266C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841329 | |||||||
| chr12:124841373 | C | CA | 72 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0094 others(69): Show |
73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.126+22221dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841373 | |||||||
| chr12:124841480 | TC | T | 4 | a0001c0005t0003g0349 a0001c0005t0004g0346 a0001c0005t0004g0347 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+22114delG | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841480 | |||||||
| chr12:124841481 | C | CA | 43 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0132 others(40): Show |
43 | HG00438.hp1 HG01099.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.126+22113dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841481 | |||||||
| chr12:124841481 | CA | C | 26 | a0001c0001t0001g0080 a0001c0001t0001g0270 a0001c0001t0003g0025 others(23): Show |
26 | HG00323.hp2 HG01243.hp1 HG01515.hp1 others(23): Show |
intron_variant | MODIFIER | c.126+22113delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841481 | |||||||
| chr12:124841482 | A | T | 4 | a0001c0005t0003g0349 a0001c0005t0004g0346 a0001c0005t0004g0347 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+22113T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841482 | |||||||
| chr12:124841535 | C | T | 1 | a0001c0002t0001g0177 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.126+22060G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841535 | |||||||
| chr12:124841569 | T | A | 1 | a0001c0004t0004g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.126+22026A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841569 | |||||||
| chr12:124841607 | T | C | 153 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0072 others(150): Show |
153 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(150): Show |
intron_variant | MODIFIER | c.126+21988A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841607 | |||||||
| chr12:124841783 | C | T | 36 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0159 others(33): Show |
36 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.126+21812G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841783 | |||||||
| chr12:124841904 | G | T | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0025g0180 others(1): Show |
4 | HG02615.hp1 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+21691C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841904 | |||||||
| chr12:124841957 | G | A | 2 | a0001c0001t0008g0027 a0003c0009t0003g0123 |
2 | HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.126+21638C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841957 | |||||||
| chr12:124841996 | G | A | 1 | a0001c0001t0003g0267 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.126+21599C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124841996 | |||||||
| chr12:124842009 | G | C | 1 | a0001c0002t0001g0189 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.126+21586C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842009 | |||||||
| chr12:124842229 | C | A | 1 | a0001c0002t0002g0088 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.126+21366G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842229 | |||||||
| chr12:124842299 | C | A | 59 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(56): Show |
59 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.126+21296G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842299 | |||||||
| chr12:124842392 | C | A | 1 | a0001c0003t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.126+21203G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842392 | |||||||
| chr12:124842464 | G | A | 4 | a0001c0001t0003g0038 a0001c0001t0003g0239 a0001c0001t0008g0330 others(1): Show |
4 | HG01361.hp1 HG02145.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+21131C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842464 | |||||||
| chr12:124842618 | G | T | 1 | a0001c0002t0001g0254 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.126+20977C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842618 | |||||||
| chr12:124842643 | C | A | 340 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(337): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.126+20952G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842643 | |||||||
| chr12:124842733 | G | A | 37 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0159 others(34): Show |
37 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.126+20862C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842733 | |||||||
| chr12:124842806 | A | G | 150 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0072 others(147): Show |
150 | HG00609.hp2 HG00621.hp2 HG00673.hp2 others(147): Show |
intron_variant | MODIFIER | c.126+20789T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842806 | |||||||
| chr12:124842838 | G | A | 151 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0072 others(148): Show |
151 | HG00609.hp2 HG00621.hp2 HG00673.hp2 others(148): Show |
intron_variant | MODIFIER | c.126+20757C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842838 | |||||||
| chr12:124842858 | C | T | 95 | a0001c0001t0001g0034 a0001c0001t0001g0050 a0001c0001t0001g0052 others(92): Show |
95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.126+20737G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842858 | |||||||
| chr12:124842880 | C | T | 16 | a0001c0001t0001g0171 a0001c0001t0001g0186 a0001c0001t0001g0206 others(13): Show |
16 | HG01069.hp2 HG01074.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.126+20715G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842880 | |||||||
| chr12:124842881 | C | T | 30 | a0001c0001t0001g0092 a0001c0001t0001g0146 a0001c0001t0001g0159 others(27): Show |
30 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+20714G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842881 | |||||||
| chr12:124842934 | T | C | 2 | a0001c0001t0008g0126 a0001c0001t0014g0127 |
2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.126+20661A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842934 | |||||||
| chr12:124842996 | G | A | 2 | a0001c0002t0001g0302 a0001c0002t0001g0303 |
2 | NA19056.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.126+20599C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124842996 | |||||||
| chr12:124843064 | G | T | 1 | a0001c0004t0004g0208 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.126+20531C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843064 | |||||||
| chr12:124843290 | T | TG | 130 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(127): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.126+20304dupC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843290 | |||||||
| chr12:124843290 | T | TGG | 42 | a0001c0001t0001g0144 a0001c0001t0001g0162 a0001c0001t0001g0298 others(39): Show |
42 | HG00621.hp2 HG01175.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.126+20303_126+2030 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843290 | |||||||
| chr12:124843299 | G | C | 1 | a0001c0020t0003g0343 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.126+20296C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843299 | |||||||
| chr12:124843299 | G | GC | 99 | a0001c0001t0001g0034 a0001c0001t0001g0050 a0001c0001t0001g0052 others(96): Show |
99 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.126+20295_126+2029 others(5): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843299 | |||||||
| chr12:124843299 | G | T | 7 | a0001c0001t0002g0335 a0001c0001t0003g0038 a0001c0001t0003g0239 others(4): Show |
7 | HG01361.hp1 HG02145.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+20296C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843299 | |||||||
| chr12:124843338 | G | T | 1 | a0001c0001t0003g0257 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.126+20257C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843338 | |||||||
| chr12:124843367 | G | A | 16 | a0001c0001t0003g0165 a0001c0001t0004g0121 a0001c0001t0016g0240 others(13): Show |
16 | HG01243.hp1 HG01891.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.126+20228C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843367 | |||||||
| chr12:124843423 | G | A | 2 | a0001c0001t0003g0029 a0002c0006t0004g0012 |
2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.126+20172C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843423 | |||||||
| chr12:124843548 | T | C | 2 | a0001c0005t0004g0347 a0001c0005t0004g0348 |
2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.126+20047A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843548 | |||||||
| chr12:124843806 | C | G | 1 | a0001c0003t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.126+19789G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843806 | |||||||
| chr12:124843829 | G | A | 57 | a0001c0001t0001g0146 a0001c0001t0001g0152 a0001c0001t0001g0159 others(54): Show |
57 | HG00673.hp2 HG00735.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.126+19766C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843829 | |||||||
| chr12:124843833 | G | A | 1 | a0001c0003t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.126+19762C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843833 | |||||||
| chr12:124843912 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0025g0180 others(1): Show |
4 | HG02615.hp1 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+19683T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843912 | |||||||
| chr12:124843924 | T | C | 1 | a0001c0002t0003g0070 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.126+19671A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124843924 | |||||||
| chr12:124844075 | G | C | 2 | a0001c0002t0001g0217 a0001c0007t0005g0191 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.126+19520C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844075 | |||||||
| chr12:124844135 | C | T | 1 | a0001c0001t0003g0284 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.126+19460G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844135 | |||||||
| chr12:124844232 | C | T | 1 | a0001c0001t0002g0310 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.126+19363G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844232 | |||||||
| chr12:124844233 | G | A | 50 | a0001c0001t0001g0092 a0001c0001t0001g0241 a0001c0001t0003g0038 others(47): Show |
51 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.126+19362C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844233 | |||||||
| chr12:124844255 | C | A | 1 | a0001c0001t0001g0228 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.126+19340G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844255 | |||||||
| chr12:124844280 | C | T | 27 | a0001c0001t0001g0146 a0001c0001t0001g0162 a0001c0001t0002g0065 others(24): Show |
27 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.126+19315G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844280 | |||||||
| chr12:124844387 | G | A | 111 | a0001c0001t0001g0019 a0001c0001t0001g0092 a0001c0001t0001g0146 others(108): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.126+19208C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844387 | |||||||
| chr12:124844686 | G | C | 54 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0094 others(51): Show |
54 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.126+18909C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844686 | |||||||
| chr12:124844748 | A | T | 4 | a0001c0001t0005g0045 a0001c0001t0005g0047 a0001c0001t0008g0046 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+18847T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844748 | |||||||
| chr12:124844767 | T | C | 150 | a0001c0001t0001g0092 a0001c0001t0001g0144 a0001c0001t0001g0146 others(147): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.126+18828A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844767 | |||||||
| chr12:124844817 | C | CT | 26 | a0001c0001t0003g0038 a0001c0001t0003g0161 a0001c0001t0003g0165 others(23): Show |
26 | HG01243.hp1 HG01361.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.126+18777dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844817 | |||||||
| chr12:124844817 | C | CTT | 50 | a0001c0001t0001g0072 a0001c0001t0001g0159 a0001c0001t0001g0270 others(47): Show |
50 | HG00609.hp2 HG00621.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.126+18776_126+1877 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844817 | |||||||
| chr12:124844817 | CT | C | 80 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0094 others(77): Show |
80 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.126+18777delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844817 | |||||||
| chr12:124844821 | T | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0052 others(88): Show |
91 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.126+18774A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844821 | |||||||
| chr12:124844822 | T | C | 1 | a0001c0010t0023g0166 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.126+18773A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844822 | |||||||
| chr12:124844884 | C | A | 1 | a0001c0002t0001g0306 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.126+18711G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124844884 | |||||||
| chr12:124845145 | C | T | 1 | a0001c0005t0001g0350 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.126+18450G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124845145 | |||||||
| chr12:124845220 | A | G | 41 | a0001c0001t0001g0146 a0001c0001t0001g0162 a0001c0001t0002g0065 others(38): Show |
41 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.126+18375T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124845220 | |||||||
| chr12:124845260 | G | C | 212 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(209): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.126+18335C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124845260 | |||||||
| chr12:124845471 | T | G | 7 | a0001c0001t0001g0272 a0001c0001t0003g0284 a0001c0002t0001g0286 others(4): Show |
7 | HG02074.hp2 NA18939.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+18124A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124845471 | |||||||
| chr12:124845537 | C | CA | 53 | a0001c0001t0001g0019 a0001c0001t0001g0072 a0001c0001t0001g0132 others(50): Show |
53 | HG00544.hp1 HG00639.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.126+18057dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124845537 | |||||||
| chr12:124845537 | C | CAA | 72 | a0001c0001t0001g0039 a0001c0001t0001g0094 a0001c0001t0001g0112 others(69): Show |
72 | HG00140.hp2 HG00544.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.126+18056_126+1805 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124845537 | |||||||
| chr12:124845537 | C | CAAA | 37 | a0001c0001t0001g0067 a0001c0001t0001g0105 a0001c0001t0001g0144 others(34): Show |
38 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(35): Show |
intron_variant | MODIFIER | c.126+18055_126+1805 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124845537 | |||||||
| chr12:124845537 | C | CAAAA | 10 | a0001c0001t0001g0040 a0001c0001t0001g0092 a0001c0001t0004g0324 others(7): Show |
10 | HG01255.hp1 HG01943.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+18054_126+1805 others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124845537 | |||||||
| chr12:124845850 | C | CA | 57 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0094 others(54): Show |
57 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.126+17744dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124845850 | |||||||
| chr12:124845944 | G | A | 2 | a0001c0001t0003g0232 a0001c0001t0008g0233 |
2 | HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.126+17651C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124845944 | |||||||
| chr12:124846059 | C | A | 1 | a0001c0001t0011g0235 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.126+17536G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846059 | |||||||
| chr12:124846095 | G | A | 19 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0165 others(16): Show |
19 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.126+17500C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846095 | |||||||
| chr12:124846356 | A | T | 27 | a0001c0001t0001g0146 a0001c0001t0001g0162 a0001c0001t0002g0065 others(24): Show |
27 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.126+17239T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846356 | |||||||
| chr12:124846478 | T | C | 51 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0094 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.126+17117A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846478 | |||||||
| chr12:124846660 | G | C | 1 | a0001c0003t0002g0056 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.126+16935C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846660 | |||||||
| chr12:124846729 | C | CA | 20 | a0001c0001t0001g0270 a0001c0001t0002g0065 a0001c0001t0004g0048 others(17): Show |
20 | HG00673.hp2 HG00735.hp2 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.126+16865dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846729 | |||||||
| chr12:124846729 | C | CAA | 53 | a0001c0001t0001g0072 a0001c0001t0001g0146 a0001c0001t0001g0159 others(50): Show |
53 | HG00609.hp2 HG00621.hp2 HG01123.hp1 others(50): Show |
intron_variant | MODIFIER | c.126+16864_126+1686 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846729 | |||||||
| chr12:124846729 | C | CAAA | 9 | a0001c0001t0001g0162 a0001c0001t0001g0326 a0001c0001t0002g0115 others(6): Show |
9 | HG01175.hp1 HG02027.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.126+16863_126+1686 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846729 | |||||||
| chr12:124846729 | CA | C | 145 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0039 others(142): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.126+16865delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846729 | |||||||
| chr12:124846729 | CAA | C | 59 | a0001c0001t0001g0052 a0001c0001t0001g0067 a0001c0001t0001g0094 others(56): Show |
59 | HG00140.hp2 HG00544.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.126+16864_126+1686 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846729 | |||||||
| chr12:124846729 | CAAA | C | 10 | a0001c0001t0001g0040 a0001c0002t0001g0097 a0001c0002t0001g0333 others(7): Show |
10 | HG01891.hp1 HG01943.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+16863_126+1686 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846729 | |||||||
| chr12:124846729 | CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0003g0232 a0001c0001t0004g0324 a0001c0001t0008g0125 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+16855_126+1686 others(15): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846729 | |||||||
| chr12:124846969 | G | A | 30 | a0001c0001t0001g0130 a0001c0001t0001g0193 a0001c0001t0001g0209 others(27): Show |
30 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.126+16626C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124846969 | |||||||
| chr12:124847068 | T | C | 7 | a0001c0001t0003g0038 a0001c0001t0003g0239 a0001c0001t0008g0330 others(4): Show |
7 | HG01361.hp1 HG02145.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+16527A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124847068 | |||||||
| chr12:124847072 | C | T | 51 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0094 others(48): Show |
51 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.126+16523G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124847072 | |||||||
| chr12:124847328 | C | T | 1 | a0001c0001t0002g0234 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.126+16267G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124847328 | |||||||
| chr12:124847429 | C | T | 8 | a0001c0001t0003g0029 a0001c0001t0003g0232 a0001c0001t0008g0125 others(5): Show |
8 | HG02257.hp1 HG02572.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+16166G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124847429 | |||||||
| chr12:124847709 | G | A | 7 | a0001c0001t0003g0038 a0001c0001t0003g0239 a0001c0001t0008g0330 others(4): Show |
7 | HG01361.hp1 HG02145.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+15886C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124847709 | |||||||
| chr12:124847979 | T | C | 1 | a0001c0003t0002g0069 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.126+15616A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124847979 | |||||||
| chr12:124848209 | G | A | 3 | a0001c0001t0001g0092 a0001c0003t0001g0307 a0001c0003t0013g0308 |
3 | HG02071.hp1 HG03654.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.126+15386C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124848209 | |||||||
| chr12:124848291 | C | T | 29 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0162 others(26): Show |
29 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.126+15304G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124848291 | |||||||
| chr12:124848409 | T | C | 248 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(245): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.126+15186A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124848409 | |||||||
| chr12:124848698 | C | T | 11 | a0001c0001t0001g0092 a0001c0001t0003g0266 a0001c0001t0003g0267 others(8): Show |
11 | HG00140.hp1 HG00621.hp1 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+14897G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124848698 | |||||||
| chr12:124848727 | G | A | 1 | a0001c0002t0007g0216 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.126+14868C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124848727 | |||||||
| chr12:124848857 | A | G | 4 | a0001c0001t0005g0045 a0001c0001t0005g0047 a0001c0001t0008g0046 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+14738T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124848857 | |||||||
| chr12:124849022 | C | A | 1 | a0001c0001t0008g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126+14573G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849022 | |||||||
| chr12:124849300 | T | C | 4 | a0001c0001t0003g0029 a0001c0001t0008g0126 a0001c0001t0014g0127 others(1): Show |
4 | HG02257.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+14295A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849300 | |||||||
| chr12:124849421 | A | G | 8 | a0001c0001t0003g0029 a0001c0001t0003g0232 a0001c0001t0008g0125 others(5): Show |
8 | HG02257.hp1 HG02572.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+14174T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849421 | |||||||
| chr12:124849434 | T | C | 33 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0162 others(30): Show |
33 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.126+14161A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849434 | |||||||
| chr12:124849522 | G | A | 214 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(211): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.126+14073C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849522 | |||||||
| chr12:124849526 | C | G | 2 | a0001c0002t0003g0138 a0001c0002t0003g0139 |
2 | HG03927.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.126+14069G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849526 | |||||||
| chr12:124849569 | G | C | 2 | a0001c0002t0001g0333 a0001c0002t0003g0249 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.126+14026C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849569 | |||||||
| chr12:124849707 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.126+13888A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849707 | |||||||
| chr12:124849764 | C | T | 1 | a0001c0003t0003g0137 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.126+13831G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849764 | |||||||
| chr12:124849768 | G | A | 1 | a0001c0002t0007g0058 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.126+13827C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849768 | |||||||
| chr12:124849772 | G | A | 33 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0162 others(30): Show |
33 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.126+13823C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849772 | |||||||
| chr12:124849822 | G | A | 1 | a0001c0001t0005g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.126+13773C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849822 | |||||||
| chr12:124849829 | A | G | 195 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(192): Show |
196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.126+13766T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849829 | |||||||
| chr12:124849850 | G | A | 2 | a0001c0001t0008g0126 a0001c0001t0014g0127 |
2 | HG02257.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.126+13745C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849850 | |||||||
| chr12:124849851 | CCAGGAGT others(303): Show |
C | 93 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0092 others(90): Show |
94 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.126+13434_126+1374 others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849851 | |||||||
| chr12:124849887 | A | T | 1 | a0001c0002t0021g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.126+13708T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849887 | |||||||
| chr12:124849894 | T | A | 33 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0162 others(30): Show |
33 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.126+13701A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124849894 | |||||||
| chr12:124850055 | C | A | 15 | a0001c0001t0001g0067 a0001c0001t0002g0065 a0001c0001t0002g0234 others(12): Show |
15 | HG00673.hp2 HG02040.hp1 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+13540G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124850055 | |||||||
| chr12:124850341 | C | T | 2 | a0001c0001t0001g0152 a0001c0002t0001g0158 |
2 | HG01106.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.126+13254G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124850341 | |||||||
| chr12:124850656 | G | T | 1 | a0001c0002t0001g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.126+12939C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124850656 | |||||||
| chr12:124850707 | C | A | 248 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(245): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.126+12888G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124850707 | |||||||
| chr12:124850745 | G | A | 4 | a0001c0001t0001g0184 a0001c0001t0001g0194 a0001c0003t0002g0136 others(1): Show |
4 | HG00544.hp1 NA18965.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+12850C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124850745 | |||||||
| chr12:124850827 | T | C | 50 | a0001c0001t0001g0040 a0001c0001t0001g0094 a0001c0001t0001g0105 others(47): Show |
50 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.126+12768A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124850827 | |||||||
| chr12:124850864 | C | T | 4 | a0001c0001t0005g0045 a0001c0001t0005g0047 a0001c0001t0008g0046 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+12731G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124850864 | |||||||
| chr12:124851347 | G | A | 2 | a0001c0002t0001g0217 a0001c0007t0005g0191 |
2 | HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.126+12248C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124851347 | |||||||
| chr12:124851404 | C | A | 33 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0162 others(30): Show |
33 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.126+12191G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124851404 | |||||||
| chr12:124851436 | C | CT | 50 | a0001c0001t0001g0040 a0001c0001t0001g0094 a0001c0001t0001g0105 others(47): Show |
50 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.126+12158dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124851436 | |||||||
| chr12:124851445 | T | C | 1 | a0001c0004t0002g0238 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.126+12150A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124851445 | |||||||
| chr12:124851545 | G | A | 8 | a0001c0001t0003g0029 a0001c0001t0003g0232 a0001c0001t0008g0125 others(5): Show |
8 | HG02257.hp1 HG02572.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.126+12050C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124851545 | |||||||
| chr12:124851608 | A | AT | 46 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0072 others(43): Show |
46 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.126+11986dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124851608 | |||||||
| chr12:124851608 | A | ATT | 30 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0002g0065 others(27): Show |
30 | HG00673.hp2 HG00735.hp2 HG01515.hp1 others(27): Show |
intron_variant | MODIFIER | c.126+11985_126+1198 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124851608 | |||||||
| chr12:124851608 | AT | A | 26 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0258 others(23): Show |
26 | HG01515.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.126+11986delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124851608 | |||||||
| chr12:124851643 | T | C | 9 | a0001c0001t0003g0029 a0001c0001t0003g0232 a0001c0001t0008g0125 others(6): Show |
9 | HG01884.hp1 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+11952A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124851643 | |||||||
| chr12:124852075 | C | T | 43 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0152 others(40): Show |
43 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.126+11520G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852075 | |||||||
| chr12:124852111 | G | C | 33 | a0001c0001t0001g0067 a0001c0001t0001g0146 a0001c0001t0001g0162 others(30): Show |
33 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.126+11484C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852111 | |||||||
| chr12:124852162 | A | G | 3 | a0001c0001t0001g0094 a0001c0002t0003g0091 a0001c0007t0001g0090 |
3 | HG02602.hp2 HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.126+11433T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852162 | |||||||
| chr12:124852219 | T | C | 54 | a0001c0001t0001g0072 a0001c0001t0001g0159 a0001c0001t0001g0270 others(51): Show |
54 | HG00609.hp2 HG00621.hp2 HG01123.hp1 others(51): Show |
intron_variant | MODIFIER | c.126+11376A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852219 | |||||||
| chr12:124852249 | C | T | 10 | a0001c0001t0001g0144 a0001c0001t0001g0241 a0001c0001t0003g0086 others(7): Show |
10 | HG00280.hp2 HG00323.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+11346G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852249 | |||||||
| chr12:124852410 | C | T | 89 | a0001c0001t0001g0034 a0001c0001t0001g0050 a0001c0001t0001g0052 others(86): Show |
89 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.126+11185G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852410 | |||||||
| chr12:124852411 | G | A | 1 | a0001c0001t0004g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.126+11184C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852411 | |||||||
| chr12:124852447 | C | T | 13 | a0001c0001t0001g0092 a0001c0001t0003g0266 a0001c0001t0003g0267 others(10): Show |
14 | HG00140.hp1 HG00621.hp1 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+11148G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852447 | |||||||
| chr12:124852537 | G | A | 3 | a0001c0001t0003g0023 a0001c0001t0003g0183 a0001c0001t0003g0328 |
3 | HG02257.hp2 HG02486.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.126+11058C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852537 | |||||||
| chr12:124852644 | G | A | 21 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0165 others(18): Show |
21 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.126+10951C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852644 | |||||||
| chr12:124852885 | A | G | 4 | a0001c0001t0003g0029 a0001c0001t0008g0126 a0001c0001t0014g0127 others(1): Show |
4 | HG02257.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+10710T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852885 | |||||||
| chr12:124852963 | G | A | 5 | a0001c0001t0001g0067 a0001c0001t0003g0068 a0001c0003t0002g0131 others(2): Show |
5 | HG00673.hp2 HG02040.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+10632C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852963 | |||||||
| chr12:124852987 | C | T | 1 | a0001c0007t0005g0191 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.126+10608G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124852987 | |||||||
| chr12:124853064 | T | C | 4 | a0001c0001t0003g0029 a0001c0001t0008g0126 a0001c0001t0014g0127 others(1): Show |
4 | HG02257.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+10531A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853064 | |||||||
| chr12:124853122 | A | T | 21 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0165 others(18): Show |
21 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.126+10473T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853122 | |||||||
| chr12:124853124 | G | T | 21 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0003g0165 others(18): Show |
21 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.126+10471C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853124 | |||||||
| chr12:124853237 | C | T | 3 | a0001c0001t0001g0092 a0001c0002t0001g0001 a0001c0002t0024g0265 |
4 | HG03239.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+10358G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853237 | |||||||
| chr12:124853385 | G | GT | 7 | a0001c0001t0001g0223 a0001c0001t0003g0117 a0001c0001t0003g0161 others(4): Show |
7 | HG02559.hp1 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.126+10209dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853385 | |||||||
| chr12:124853389 | T | TG | 11 | a0001c0001t0001g0159 a0001c0001t0002g0116 a0001c0001t0002g0157 others(8): Show |
11 | HG00609.hp2 HG02040.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+10205dupC | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853389 | |||||||
| chr12:124853390 | G | GT | 18 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0184 others(15): Show |
18 | HG00438.hp2 HG00544.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.126+10204dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853390 | |||||||
| chr12:124853390 | G | T | 23 | a0001c0001t0001g0223 a0001c0001t0003g0023 a0001c0001t0003g0117 others(20): Show |
23 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.126+10205C>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853390 | |||||||
| chr12:124853390 | GT | G | 84 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0144 others(81): Show |
85 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.126+10204delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853390 | |||||||
| chr12:124853390 | GTT | G | 32 | a0001c0001t0001g0067 a0001c0001t0001g0094 a0001c0001t0001g0146 others(29): Show |
32 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.126+10203_126+1020 others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853390 | |||||||
| chr12:124853390 | GTTT | G | 37 | a0001c0001t0001g0040 a0001c0001t0001g0105 a0001c0001t0001g0112 others(34): Show |
37 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.126+10202_126+1020 others(7): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853390 | |||||||
| chr12:124853391 | T | G | 44 | a0001c0001t0001g0072 a0001c0001t0001g0270 a0001c0001t0001g0272 others(41): Show |
44 | HG00621.hp2 HG01123.hp1 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.126+10204A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853391 | |||||||
| chr12:124853392 | T | G | 10 | a0001c0001t0001g0132 a0001c0001t0001g0171 a0001c0001t0003g0029 others(7): Show |
10 | HG01081.hp1 HG02257.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+10203A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853392 | |||||||
| chr12:124853393 | T | G | 42 | a0001c0001t0001g0039 a0001c0001t0001g0152 a0001c0001t0001g0173 others(39): Show |
42 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.126+10202A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853393 | |||||||
| chr12:124853395 | T | G | 1 | a0001c0001t0003g0165 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.126+10200A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853395 | |||||||
| chr12:124853396 | T | G | 1 | a0001c0001t0004g0324 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.126+10199A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853396 | |||||||
| chr12:124853418 | G | A | 10 | a0001c0001t0001g0144 a0001c0001t0001g0241 a0001c0001t0003g0086 others(7): Show |
10 | HG00280.hp2 HG00323.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.126+10177C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853418 | |||||||
| chr12:124853487 | C | T | 1 | a0001c0007t0001g0063 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.126+10108G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853487 | |||||||
| chr12:124853551 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.126+10044G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853551 | |||||||
| chr12:124853560 | A | G | 1 | a0001c0001t0017g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.126+10035T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853560 | |||||||
| chr12:124853639 | C | G | 1 | a0001c0001t0008g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.126+9956G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853639 | |||||||
| chr12:124853704 | T | C | 4 | a0001c0001t0005g0045 a0001c0001t0005g0047 a0001c0001t0008g0046 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+9891A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853704 | |||||||
| chr12:124853790 | T | C | 41 | a0001c0001t0001g0040 a0001c0001t0001g0094 a0001c0001t0001g0105 others(38): Show |
41 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.126+9805A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853790 | |||||||
| chr12:124853843 | G | A | 2 | a0001c0001t0003g0025 a0001c0001t0004g0026 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.126+9752C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853843 | |||||||
| chr12:124853853 | G | A | 2 | a0001c0010t0023g0166 a0003c0009t0001g0222 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.126+9742C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853853 | |||||||
| chr12:124853983 | C | T | 203 | a0001c0001t0001g0019 a0001c0001t0001g0034 a0001c0001t0001g0040 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.126+9612G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853983 | |||||||
| chr12:124853993 | G | C | 1 | a0001c0005t0006g0344 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.126+9602C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124853993 | |||||||
| chr12:124854231 | G | A | 49 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0152 others(46): Show |
49 | HG00639.hp2 HG00738.hp1 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.126+9364C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854231 | |||||||
| chr12:124854288 | C | T | 2 | a0001c0001t0003g0025 a0001c0001t0004g0026 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.126+9307G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854288 | |||||||
| chr12:124854318 | A | C | 2 | a0001c0001t0003g0025 a0001c0001t0004g0026 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.126+9277T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854318 | |||||||
| chr12:124854341 | C | G | 242 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(239): Show |
243 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.126+9254G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854341 | |||||||
| chr12:124854345 | C | T | 52 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0146 others(49): Show |
53 | HG00099.hp2 HG00140.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.126+9250G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854345 | |||||||
| chr12:124854388 | C | T | 2 | a0001c0001t0003g0232 a0001c0001t0008g0233 |
2 | HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.126+9207G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854388 | |||||||
| chr12:124854549 | G | A | 39 | a0001c0001t0001g0040 a0001c0001t0001g0092 a0001c0001t0001g0094 others(36): Show |
39 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.126+9046C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854549 | |||||||
| chr12:124854557 | G | C | 14 | a0001c0001t0001g0080 a0001c0001t0001g0144 a0001c0001t0001g0241 others(11): Show |
14 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+9038C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854557 | |||||||
| chr12:124854571 | G | A | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.126+9024C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854571 | |||||||
| chr12:124854672 | G | A | 1 | a0001c0004t0004g0230 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.126+8923C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854672 | |||||||
| chr12:124854682 | A | C | 247 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(244): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.126+8913T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854682 | |||||||
| chr12:124854699 | A | G | 53 | a0001c0001t0001g0072 a0001c0001t0001g0159 a0001c0001t0001g0272 others(50): Show |
53 | HG00609.hp2 HG00621.hp2 HG01123.hp1 others(50): Show |
intron_variant | MODIFIER | c.126+8896T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854699 | |||||||
| chr12:124854743 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.126+8852T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854743 | |||||||
| chr12:124854793 | C | T | 1 | a0001c0001t0003g0025 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.126+8802G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854793 | |||||||
| chr12:124854819 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+8776G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854819 | |||||||
| chr12:124854855 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0006g0035 a0001c0001t0008g0036 others(1): Show |
4 | HG03471.hp1 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.126+8740C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854855 | |||||||
| chr12:124854858 | C | T | 2 | a0001c0001t0001g0080 a0001c0002t0001g0081 |
2 | HG00140.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.126+8737G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124854858 | |||||||
| chr12:124855093 | G | A | 1 | a0002c0006t0001g0013 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.126+8502C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124855093 | |||||||
| chr12:124855298 | G | A | 1 | a0001c0003t0002g0319 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.126+8297C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124855298 | |||||||
| chr12:124855304 | G | A | 1 | a0001c0002t0007g0058 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.126+8291C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124855304 | |||||||
| chr12:124855333 | G | A | 14 | a0001c0001t0001g0270 a0001c0001t0003g0025 a0001c0001t0003g0266 others(11): Show |
15 | HG00621.hp1 HG02698.hp2 HG03139.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+8262C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124855333 | |||||||
| chr12:124855399 | C | T | 1 | a0001c0001t0008g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.126+8196G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124855399 | |||||||
| chr12:124855444 | T | C | 43 | a0001c0001t0001g0040 a0001c0001t0001g0092 a0001c0001t0001g0094 others(40): Show |
43 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.126+8151A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124855444 | |||||||
| chr12:124855576 | G | A | 42 | a0001c0001t0001g0040 a0001c0001t0001g0092 a0001c0001t0001g0094 others(39): Show |
42 | HG00544.hp2 HG00639.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.126+8019C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124855576 | |||||||
| chr12:124855849 | G | A | 1 | a0001c0001t0018g0071 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.126+7746C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124855849 | |||||||
| chr12:124855901 | G | A | 224 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(221): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.126+7694C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124855901 | |||||||
| chr12:124855990 | G | A | 1 | a0001c0001t0022g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.126+7605C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124855990 | |||||||
| chr12:124856096 | A | C | 1 | a0001c0001t0008g0027 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.126+7499T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124856096 | |||||||
| chr12:124856630 | G | A | 1 | a0001c0002t0001g0252 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.126+6965C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124856630 | |||||||
| chr12:124856717 | C | T | 1 | a0001c0003t0002g0263 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.126+6878G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124856717 | |||||||
| chr12:124856743 | C | G | 9 | a0001c0001t0001g0072 a0001c0001t0002g0335 a0001c0001t0018g0071 others(6): Show |
9 | HG01070.hp1 HG01123.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.126+6852G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124856743 | |||||||
| chr12:124856743 | C | T | 11 | a0001c0001t0001g0132 a0001c0001t0003g0025 a0001c0001t0003g0169 others(8): Show |
11 | HG00544.hp1 HG00597.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+6852G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124856743 | |||||||
| chr12:124856749 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0002g0116 |
2 | HG02056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.126+6846C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124856749 | |||||||
| chr12:124856780 | C | T | 1 | a0002c0006t0001g0002 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.126+6815G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124856780 | |||||||
| chr12:124856784 | C | T | 1 | a0001c0001t0002g0253 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.126+6811G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124856784 | |||||||
| chr12:124856858 | C | T | 1 | a0003c0009t0003g0123 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.126+6737G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124856858 | |||||||
| chr12:124856941 | T | G | 1 | a0002c0008t0003g0015 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.126+6654A>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124856941 | |||||||
| chr12:124857006 | C | T | 1 | a0001c0001t0003g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.126+6589G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857006 | |||||||
| chr12:124857022 | A | G | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.126+6573T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857022 | |||||||
| chr12:124857124 | G | A | 8 | a0001c0001t0004g0124 a0001c0001t0008g0125 a0001c0001t0008g0126 others(5): Show |
8 | HG01109.hp1 HG01884.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.126+6471C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857124 | |||||||
| chr12:124857226 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.126+6369G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857226 | |||||||
| chr12:124857300 | C | A | 1 | a0001c0003t0002g0110 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.126+6295G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857300 | |||||||
| chr12:124857324 | C | T | 65 | a0001c0001t0001g0072 a0001c0001t0001g0080 a0001c0001t0001g0092 others(62): Show |
65 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.126+6271G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857324 | |||||||
| chr12:124857440 | G | C | 1 | a0001c0001t0005g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.126+6155C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857440 | |||||||
| chr12:124857450 | C | T | 1 | a0001c0001t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.126+6145G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857450 | |||||||
| chr12:124857492 | G | C | 1 | a0001c0001t0004g0121 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.126+6103C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857492 | |||||||
| chr12:124857537 | C | T | 60 | a0001c0001t0001g0272 a0001c0001t0001g0279 a0001c0001t0001g0281 others(57): Show |
60 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.126+6058G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857537 | |||||||
| chr12:124857587 | C | T | 14 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0003g0140 others(11): Show |
14 | HG00544.hp1 HG02165.hp2 HG03654.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+6008G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857587 | |||||||
| chr12:124857635 | A | G | 6 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0006g0022 others(3): Show |
6 | HG01884.hp1 HG02723.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+5960T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857635 | |||||||
| chr12:124857796 | A | G | 1 | a0001c0002t0003g0070 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.126+5799T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857796 | |||||||
| chr12:124857994 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.126+5601G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124857994 | |||||||
| chr12:124858176 | C | T | 1 | a0001c0003t0002g0069 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.126+5419G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858176 | |||||||
| chr12:124858355 | T | A | 11 | a0001c0001t0001g0270 a0001c0001t0003g0266 a0001c0001t0003g0267 others(8): Show |
12 | HG00621.hp1 HG02818.hp2 HG03239.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+5240A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858355 | |||||||
| chr12:124858374 | G | A | 73 | a0001c0001t0001g0072 a0001c0001t0001g0080 a0001c0001t0001g0092 others(70): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.126+5221C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858374 | |||||||
| chr12:124858377 | G | A | 1 | a0001c0018t0006g0340 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.126+5218C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858377 | |||||||
| chr12:124858426 | A | G | 26 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0270 others(23): Show |
27 | HG00544.hp1 HG00621.hp1 HG02165.hp2 others(24): Show |
intron_variant | MODIFIER | c.126+5169T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858426 | |||||||
| chr12:124858554 | T | C | 1 | a0001c0001t0002g0253 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.126+5041A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858554 | |||||||
| chr12:124858568 | C | T | 1 | a0001c0004t0002g0271 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.126+5027G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858568 | |||||||
| chr12:124858654 | C | T | 10 | a0001c0001t0001g0152 a0001c0001t0001g0159 a0001c0001t0002g0157 others(7): Show |
10 | HG01106.hp2 HG01243.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.126+4941G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858654 | |||||||
| chr12:124858702 | A | G | 228 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(225): Show |
228 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.126+4893T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858702 | |||||||
| chr12:124858741 | C | T | 229 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0050 others(226): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.126+4854G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858741 | |||||||
| chr12:124858752 | G | A | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.126+4843C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858752 | |||||||
| chr12:124858804 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.126+4791C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858804 | |||||||
| chr12:124858836 | A | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0003g0038 others(4): Show |
7 | HG01361.hp1 HG01943.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+4759T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858836 | |||||||
| chr12:124858874 | G | A | 1 | a0001c0013t0016g0334 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.126+4721C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858874 | |||||||
| chr12:124858956 | C | G | 3 | a0001c0001t0012g0060 a0001c0001t0012g0062 a0001c0001t0019g0061 |
3 | HG02451.hp1 HG02615.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.126+4639G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858956 | |||||||
| chr12:124858959 | C | T | 1 | a0001c0003t0002g0167 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.126+4636G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124858959 | |||||||
| chr12:124859245 | T | C | 1 | a0001c0002t0005g0255 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.126+4350A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859245 | |||||||
| chr12:124859249 | C | T | 1 | a0001c0010t0023g0166 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.126+4346G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859249 | |||||||
| chr12:124859332 | C | G | 1 | a0001c0004t0015g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.126+4263G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859332 | |||||||
| chr12:124859334 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.126+4261G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859334 | |||||||
| chr12:124859480 | G | A | 1 | a0001c0001t0008g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.126+4115C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859480 | |||||||
| chr12:124859518 | G | C | 60 | a0001c0001t0001g0272 a0001c0001t0001g0279 a0001c0001t0001g0281 others(57): Show |
60 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.126+4077C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859518 | |||||||
| chr12:124859537 | GA | G | 328 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0040 others(325): Show |
329 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.126+4057delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859537 | |||||||
| chr12:124859537 | GAA | G | 19 | a0001c0001t0003g0117 a0001c0001t0004g0121 a0001c0001t0006g0118 others(16): Show |
19 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.126+4056_126+4057d others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859537 | |||||||
| chr12:124859547 | A | G | 19 | a0001c0001t0003g0117 a0001c0001t0004g0121 a0001c0001t0006g0118 others(16): Show |
19 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.126+4048T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859547 | |||||||
| chr12:124859619 | A | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0003g0038 others(4): Show |
7 | HG01361.hp1 HG01943.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+3976T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859619 | |||||||
| chr12:124859629 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0003g0038 others(4): Show |
7 | HG01361.hp1 HG01943.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.126+3966C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859629 | |||||||
| chr12:124859695 | C | T | 5 | a0001c0001t0004g0124 a0001c0001t0008g0125 a0001c0001t0008g0126 others(2): Show |
5 | HG01109.hp1 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.126+3900G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859695 | |||||||
| chr12:124859745 | G | A | 208 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(205): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.126+3850C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859745 | |||||||
| chr12:124859793 | G | A | 208 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(205): Show |
208 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.126+3802C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859793 | |||||||
| chr12:124859795 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.126+3800G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859795 | |||||||
| chr12:124859919 | C | T | 19 | a0001c0001t0003g0117 a0001c0001t0004g0121 a0001c0001t0006g0118 others(16): Show |
19 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.126+3676G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859919 | |||||||
| chr12:124859949 | A | AT | 75 | a0001c0001t0001g0019 a0001c0001t0001g0067 a0001c0001t0001g0072 others(72): Show |
75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.126+3645dupA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859949 | |||||||
| chr12:124859949 | AT | A | 123 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(120): Show |
123 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.126+3645delA | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859949 | |||||||
| chr12:124859949 | ATT | A | 112 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0258 others(109): Show |
113 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.126+3644_126+3645d others(4): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124859949 | |||||||
| chr12:124860012 | G | A | 12 | a0001c0001t0004g0324 a0001c0005t0001g0350 a0001c0005t0003g0349 others(9): Show |
12 | HG01891.hp1 HG02280.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+3583C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124860012 | |||||||
| chr12:124860271 | G | A | 1 | a0001c0001t0017g0028 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.126+3324C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124860271 | |||||||
| chr12:124860385 | G | A | 1 | a0001c0002t0021g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.126+3210C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124860385 | |||||||
| chr12:124860428 | A | G | 1 | a0001c0001t0003g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.126+3167T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124860428 | |||||||
| chr12:124860614 | A | T | 1 | a0001c0003t0002g0261 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.126+2981T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124860614 | |||||||
| chr12:124860852 | C | T | 1 | a0001c0017t0005g0341 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+2743G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124860852 | |||||||
| chr12:124860902 | A | G | 138 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(135): Show |
138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.126+2693T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124860902 | |||||||
| chr12:124861097 | G | A | 240 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0052 others(237): Show |
241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.126+2498C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861097 | |||||||
| chr12:124861238 | G | A | 70 | a0001c0001t0001g0067 a0001c0001t0001g0072 a0001c0001t0001g0080 others(67): Show |
70 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.126+2357C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861238 | |||||||
| chr12:124861284 | C | T | 1 | a0001c0003t0002g0149 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.126+2311G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861284 | |||||||
| chr12:124861298 | A | T | 1 | a0001c0001t0002g0335 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.126+2297T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861298 | |||||||
| chr12:124861336 | G | C | 4 | a0001c0001t0005g0045 a0001c0001t0005g0047 a0001c0001t0008g0046 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+2259C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861336 | |||||||
| chr12:124861370 | T | A | 1 | a0001c0001t0002g0335 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.126+2225A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861370 | |||||||
| chr12:124861389 | A | C | 15 | a0001c0002t0001g0049 a0002c0006t0001g0002 a0002c0006t0001g0003 others(12): Show |
15 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.126+2206T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861389 | |||||||
| chr12:124861433 | G | A | 1 | a0001c0001t0001g0326 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.126+2162C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861433 | |||||||
| chr12:124861474 | C | T | 340 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0052 others(337): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.126+2121G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861474 | |||||||
| chr12:124861477 | TA | T | 78 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(75): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.126+2117delT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861477 | |||||||
| chr12:124861486 | A | T | 1 | a0001c0001t0004g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.126+2109T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861486 | |||||||
| chr12:124861487 | A | T | 126 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0152 others(123): Show |
126 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.126+2108T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861487 | |||||||
| chr12:124861526 | A | G | 1 | a0001c0002t0001g0147 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.126+2069T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861526 | |||||||
| chr12:124861683 | G | A | 1 | a0001c0003t0002g0129 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.126+1912C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861683 | |||||||
| chr12:124861876 | G | GCACA | 207 | a0001c0001t0001g0019 a0001c0001t0001g0145 a0001c0001t0001g0152 others(204): Show |
208 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.126+1715_126+1718d others(6): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861876 | |||||||
| chr12:124861876 | G | GCACACA | 20 | a0001c0001t0003g0328 a0001c0001t0004g0329 a0001c0001t0008g0330 others(17): Show |
20 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.126+1713_126+1718d others(8): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861876 | |||||||
| chr12:124861895 | T | C | 340 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0052 others(337): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.126+1700A>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861895 | |||||||
| chr12:124861959 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.126+1636T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124861959 | |||||||
| chr12:124862032 | C | CA | 228 | a0001c0001t0001g0019 a0001c0001t0001g0145 a0001c0001t0001g0146 others(225): Show |
229 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.126+1562dupT | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124862032 | |||||||
| chr12:124862093 | C | T | 14 | a0002c0006t0001g0002 a0002c0006t0001g0003 a0002c0006t0001g0004 others(11): Show |
14 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.126+1502G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124862093 | |||||||
| chr12:124862265 | A | G | 2 | a0001c0001t0008g0027 a0001c0001t0017g0028 |
2 | HG01884.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.126+1330T>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124862265 | |||||||
| chr12:124862281 | G | A | 1 | a0001c0002t0001g0333 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.126+1314C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124862281 | |||||||
| chr12:124862616 | C | T | 6 | a0001c0001t0005g0045 a0001c0001t0005g0047 a0001c0001t0008g0046 others(3): Show |
6 | HG02109.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.126+979G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124862616 | |||||||
| chr12:124862692 | TC | T | 340 | a0001c0001t0001g0019 a0001c0001t0001g0050 a0001c0001t0001g0052 others(337): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.126+902delG | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124862692 | |||||||
| chr12:124862694 | C | T | 16 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0003g0025 others(13): Show |
16 | HG00544.hp1 HG02040.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.126+901G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124862694 | |||||||
| chr12:124862707 | A | T | 1 | a0001c0001t0001g0130 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.126+888T>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124862707 | |||||||
| chr12:124862758 | T | TC | 111 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(108): Show |
111 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.126+836dupG | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124862758 | |||||||
| chr12:124862920 | A | C | 19 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0003g0025 others(16): Show |
19 | HG00544.hp1 HG01884.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.126+675T>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124862920 | |||||||
| chr12:124863005 | G | A | 14 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0003g0140 others(11): Show |
14 | HG00544.hp1 HG02040.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.126+590C>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124863005 | |||||||
| chr12:124863019 | G | C | 1 | a0001c0017t0005g0341 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+576C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124863019 | |||||||
| chr12:124863141 | C | A | 1 | a0001c0001t0002g0335 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.126+454G>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124863141 | |||||||
| chr12:124863218 | T | TCA | 230 | a0001c0001t0001g0019 a0001c0001t0001g0144 a0001c0001t0001g0145 others(227): Show |
231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.126+375_126+376dup others(2): Show |
SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124863218 | |||||||
| chr12:124863270 | C | T | 1 | a0001c0001t0006g0024 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.126+325G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124863270 | |||||||
| chr12:124863317 | C | G | 1 | a0001c0001t0003g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.126+278G>C | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124863317 | |||||||
| chr12:124863334 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0003g0020 a0001c0001t0006g0022 others(1): Show |
4 | HG03041.hp2 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+261G>A | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124863334 | |||||||
| chr12:124863380 | T | A | 3 | a0001c0002t0005g0336 a0001c0002t0005g0337 a0001c0002t0005g0338 |
3 | HG03491.hp1 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.126+215A>T | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124863380 | |||||||
| chr12:124863578 | G | C | 1 | a0001c0003t0013g0339 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.126+17C>G | SCARB1 | ENSG00000073060.17 | transcript | ENST00000261693.11 | protein_coding | 1/12 | chr12 | 124863578 |