Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79634 |
| ensemblid | ENSG00000144306.15 |
| hgncid | 30382 |
| symbol | SCRN3 |
| name | secernin 3 |
| refseq_nuc | NM_024583.5 |
| refseq_prot | NP_078859.2 |
| ensembl_nuc | ENST00000272732.11 |
| ensembl_prot | ENSP00000272732.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 174395730 |
| end | 174429575 |
| strand | + |
| ver | v1.2 |
| region | chr2:174395730-174429575 |
| region5000 | chr2:174390730-174434575 |
| regionname0 | SCRN3_chr2_174395730_174429575 |
| regionname5000 | SCRN3_chr2_174390730_174434575 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 424 | 238 | 83 | 39 | 80 | 7 | 28 | 65 | SCRN3_chr2_174390730_174434575 | SCRN3 | MEPFS others(419): Show |
chr2 | 174390730 | 174434575 |
| a0002 | 0/1 | 419 | 87 | 4 | 15 | 45 | 7 | 15 | 38 | SCRN3_chr2_174390730_174434575 | SCRN3 | MEPFS others(414): Show |
chr2 | 174390730 | 174434575 |
| a0003 | 0/0 | 424 | 29 | 1 | 21 | 0 | 4 | 3 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | MEPFS others(419): Show |
chr2 | 174390730 | 174434575 |
| a0004 | 0/0 | 424 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | MEPFS others(419): Show |
chr2 | 174390730 | 174434575 |
| a0005 | 0/0 | 424 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | MEPFS others(419): Show |
chr2 | 174390730 | 174434575 |
| a0006 | 0/0 | 424 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | MEPFS others(419): Show |
chr2 | 174390730 | 174434575 |
| a0007 | 0/0 | 424 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | MEPFS others(419): Show |
chr2 | 174390730 | 174434575 |
| a0008 | 0/0 | 424 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | MEPFS others(419): Show |
chr2 | 174390730 | 174434575 |
| a0009 | 0/0 | 419 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | MEPFS others(414): Show |
chr2 | 174390730 | 174434575 |
| a0010 | 0/0 | 424 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | MEPFS others(419): Show |
chr2 | 174390730 | 174434575 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1272 | 234 | 79 | 39 | 80 | 7 | 28 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATGGA others(1267): Show |
chr2 | 174390730 | 174434575 | ||
| a0001c0005 | 0/0 | 1272 | 4 | 4 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATGGA others(1267): Show |
chr2 | 174390730 | 174434575 | ||
| a0002c0002 | 0/0 | 1259 | 72 | 4 | 10 | 45 | 5 | 8 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATGGA others(1254): Show |
chr2 | 174390730 | 174434575 | ||
| a0002c0004 | 0/1 | 1259 | 15 | 0 | 5 | 0 | 2 | 7 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATGGA others(1254): Show |
chr2 | 174390730 | 174434575 | ||
| a0003c0003 | 0/0 | 1272 | 29 | 1 | 21 | 0 | 4 | 3 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATGGA others(1267): Show |
chr2 | 174390730 | 174434575 | ||
| a0004c0006 | 0/0 | 1272 | 3 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATGGA others(1267): Show |
chr2 | 174390730 | 174434575 | ||
| a0005c0007 | 0/0 | 1272 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATGGA others(1267): Show |
chr2 | 174390730 | 174434575 | ||
| a0006c0011 | 0/0 | 1272 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATGGA others(1267): Show |
chr2 | 174390730 | 174434575 | ||
| a0007c0010 | 0/0 | 1272 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATGGA others(1267): Show |
chr2 | 174390730 | 174434575 | ||
| a0008c0012 | 0/0 | 1272 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATGGA others(1267): Show |
chr2 | 174390730 | 174434575 | ||
| a0009c0008 | 0/0 | 1259 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATGGA others(1254): Show |
chr2 | 174390730 | 174434575 | ||
| a0010c0009 | 0/0 | 1272 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATGGA others(1267): Show |
chr2 | 174390730 | 174434575 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3052 | 192 | 45 | 38 | 76 | 7 | 25 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0001c0001t0003 | 0/0 | 3052 | 18 | 17 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0001c0001t0005 | 0/0 | 3052 | 8 | 7 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0001c0001t0006 | 0/0 | 3052 | 5 | 5 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCTA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0001c0001t0007 | 0/0 | 3052 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0001c0001t0008 | 0/0 | 3052 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0001c0001t0009 | 0/0 | 3052 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0001c0001t0011 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0001c0001t0013 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0001c0001t0016 | 0/0 | 3052 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0001c0001t0017 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0001c0001t0018 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCTA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0001c0005t0001 | 0/0 | 3052 | 4 | 4 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0002c0002t0002 | 0/0 | 3039 | 54 | 3 | 4 | 45 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3034): Show |
chr2 | 174390730 | 174434575 |
| a0002c0002t0004 | 0/0 | 3039 | 17 | 1 | 6 | 0 | 4 | 6 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3034): Show |
chr2 | 174390730 | 174434575 |
| a0002c0002t0012 | 0/0 | 3039 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3034): Show |
chr2 | 174390730 | 174434575 |
| a0002c0004t0002 | 0/1 | 3039 | 15 | 0 | 5 | 0 | 2 | 7 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3034): Show |
chr2 | 174390730 | 174434575 |
| a0003c0003t0001 | 0/0 | 3052 | 27 | 1 | 19 | 0 | 4 | 3 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0003c0003t0014 | 0/0 | 3052 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0003c0003t0015 | 0/0 | 3052 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0004c0006t0001 | 0/0 | 3052 | 3 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0005c0007t0010 | 0/0 | 3052 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0006c0011t0001 | 0/0 | 3052 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0007c0010t0001 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0008c0012t0001 | 0/0 | 3052 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| a0009c0008t0002 | 0/0 | 3039 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3034): Show |
chr2 | 174390730 | 174434575 |
| a0010c0009t0001 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | ATCAA others(3047): Show |
chr2 | 174390730 | 174434575 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 0 | 1 | 7 | 1 | 3 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0018 | 1/0 | 3 | 1 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0005g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0008g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0009g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0013g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0016g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0017g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0001t0018g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0005t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0005t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0002 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0004g0006 | 0/0 | 6 | 0 | 3 | 0 | 0 | 3 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0004g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0002t0012g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0004t0002g0012 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0004t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0004t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0004t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0004t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0004t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0004t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0002c0004t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0004 | 0/0 | 7 | 1 | 6 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0014g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0003c0003t0015g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0004c0006t0001g0022 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0005c0007t0010g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0005c0007t0010g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0006c0011t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0007c0010t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0008c0012t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0009c0008t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| a0010c0009t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | GBR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00323 | hp2 | a0002 | c0002 | t0004 | g0063 | EUR | FIN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00639 | hp2 | a0002 | c0002 | t0004 | g0006 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0066 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00733 | hp2 | a0002 | c0004 | t0002 | g0012 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00735 | hp1 | a0002 | c0004 | t0002 | g0075 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00738 | hp1 | a0004 | c0006 | t0001 | g0022 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00741 | hp1 | a0002 | c0004 | t0002 | g0012 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG00741 | hp2 | a0003 | c0003 | t0014 | g0136 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01069 | hp1 | a0003 | c0003 | t0001 | g0140 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0138 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01070 | hp2 | a0002 | c0004 | t0002 | g0076 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01074 | hp2 | a0003 | c0003 | t0001 | g0035 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01081 | hp2 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01099 | hp2 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0139 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01109 | hp1 | a0003 | c0003 | t0015 | g0124 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01109 | hp2 | a0002 | c0002 | t0004 | g0024 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0004 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0134 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0130 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0141 | AMR | PUR | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01255 | hp2 | a0003 | c0003 | t0001 | g0125 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01256 | hp1 | a0002 | c0002 | t0004 | g0006 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0127 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01258 | hp1 | a0002 | c0002 | t0004 | g0006 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0067 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01433 | hp2 | a0002 | c0002 | t0004 | g0060 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01496 | hp1 | a0002 | c0004 | t0002 | g0079 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01496 | hp2 | a0004 | c0006 | t0001 | g0022 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01515 | hp1 | a0003 | c0003 | t0001 | g0128 | EUR | IBS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01515 | hp2 | a0002 | c0002 | t0004 | g0062 | EUR | IBS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01516 | hp1 | a0002 | c0004 | t0002 | g0078 | EUR | IBS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0035 | EUR | IBS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01517 | hp1 | a0002 | c0004 | t0002 | g0077 | EUR | IBS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0129 | EUR | IBS | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0228 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01891 | hp2 | a0001 | c0005 | t0001 | g0158 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01952 | hp2 | a0006 | c0011 | t0001 | g0175 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0213 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0019 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01981 | hp1 | a0003 | c0003 | t0001 | g0126 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CDX | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0232 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02300 | hp1 | a0002 | c0002 | t0004 | g0065 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0086 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0223 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02602 | hp1 | a0001 | c0001 | t0016 | g0188 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02622 | hp1 | a0001 | c0005 | t0001 | g0160 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0004 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0108 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0019 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02683 | hp2 | a0002 | c0004 | t0002 | g0074 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02698 | hp1 | a0002 | c0002 | t0004 | g0061 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0231 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02735 | hp1 | a0002 | c0004 | t0002 | g0081 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02738 | hp1 | a0002 | c0004 | t0002 | g0071 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0088 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0089 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0117 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02976 | hp2 | a0001 | c0001 | t0018 | g0083 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03017 | hp2 | a0002 | c0002 | t0004 | g0006 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0230 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03098 | hp2 | a0001 | c0005 | t0001 | g0157 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0085 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03209 | hp2 | a0007 | c0010 | t0001 | g0148 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0011 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0208 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03490 | hp2 | a0002 | c0002 | t0004 | g0006 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03491 | hp2 | a0002 | c0004 | t0002 | g0025 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03492 | hp1 | a0002 | c0004 | t0002 | g0025 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03492 | hp2 | a0002 | c0002 | t0004 | g0006 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0233 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03579 | hp2 | a0001 | c0005 | t0001 | g0159 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0019 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03704 | hp1 | a0001 | c0001 | t0009 | g0187 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03710 | hp1 | a0004 | c0006 | t0001 | g0022 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0135 | SAS | PJL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03831 | hp2 | a0002 | c0004 | t0002 | g0073 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03927 | hp1 | a0008 | c0012 | t0001 | g0201 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG04184 | hp1 | a0002 | c0002 | t0004 | g0069 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | BEB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG04199 | hp2 | a0002 | c0002 | t0004 | g0024 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG04204 | hp1 | a0001 | c0001 | t0009 | g0001 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0225 | SAS | STU | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0059 | AFR | YRI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | YRI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18964 | hp1 | a0005 | c0007 | t0010 | g0110 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18979 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18988 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18994 | hp2 | a0001 | c0001 | t0017 | g0015 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19000 | hp2 | a0001 | c0001 | t0008 | g0015 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0224 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19030 | hp1 | a0009 | c0008 | t0002 | g0146 | AFR | LWK | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0214 | AFR | LWK | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19060 | hp1 | a0010 | c0009 | t0001 | g0168 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19076 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19089 | hp2 | a0005 | c0007 | t0010 | g0109 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ASW | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0156 | AFR | ASW | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0137 | EUR | TSI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA20752 | hp2 | a0002 | c0002 | t0004 | g0070 | EUR | TSI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA20805 | hp1 | a0002 | c0002 | t0012 | g0011 | EUR | TSI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA20805 | hp2 | a0002 | c0002 | t0004 | g0064 | EUR | TSI | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA20905 | hp1 | a0002 | c0004 | t0002 | g0012 | SAS | GIH | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | GIH | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01123 | hp1 | a0003 | c0003 | t0001 | g0131 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0057 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | USA | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | USA | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | LWK | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| NA21309 | hp2 | a0001 | c0001 | t0013 | g0229 | AFR | LWK | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| homoSapiens | chm13v2 | a0002 | c0004 | t0002 | g0012 | REF | REF | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0018 | REF | REF | SCRN3_chr2_174390730_174434575 | SCRN3 | chr2 | 174390730 | 174434575 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:174398335 | G | A | 1 | a0003 | 29 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(26): Show |
missense_variant | MODERATE | c.52G>A | p.Asp18Asn | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/8 | 149/3052 | 52/1275 | 18/424 | chr2 | 174398335 | |||
| chr2:174399983 | C | T | 1 | a0008 | 1 | HG03927.hp1 | missense_variant | MODERATE | c.221C>T | p.Ala74Val | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/8 | 318/3052 | 221/1275 | 74/424 | chr2 | 174399983 | |||
| chr2:174401184 | T | C | 1 | a0009 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.536T>C | p.Val179Ala | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/8 | 633/3052 | 536/1275 | 179/424 | chr2 | 174401184 | |||
| chr2:174404132 | T | G | 1 | a0010 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.571T>G | p.Ser191Ala | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/8 | 668/3052 | 571/1275 | 191/424 | chr2 | 174404132 | |||
| chr2:174422999 | C | G | 1 | a0006 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.869C>G | p.Ser290Cys | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/8 | 966/3052 | 869/1275 | 290/424 | chr2 | 174422999 | |||
| chr2:174424531 | G | T | 1 | a0004 | 3 | HG00738.hp1 HG01496.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.974G>T | p.Ser325Ile | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/8 | 1071/3052 | 974/1275 | 325/424 | chr2 | 174424531 | |||
| chr2:174427785 | C | T | 1 | a0007 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1165C>T | p.Leu389Phe | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1262/3052 | 1165/1275 | 389/424 | chr2 | 174427785 | |||
| chr2:174427852 | TTCAAATT others(6): Show |
T | 2 | a0002 a0009 |
87 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
frameshift_variant | HIGH | c.1251_1263delTTTATC others(7): Show |
p.Asn417fs | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1348/3052 | 1251/1275 | 417/424 | INFO_REALIGN_3_PRIME | chr2 | 174427852 | ||
| chr2:174427882 | A | T | 1 | a0005 | 2 | NA18964.hp1 NA19089.hp2 |
missense_variant | MODERATE | c.1262A>T | p.Lys421Ile | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1359/3052 | 1262/1275 | 421/424 | chr2 | 174427882 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:174398334 | C | T | 1 | a0001c0005 | 4 | HG01891.hp2 HG02622.hp1 HG03098.hp2 others(1): Show |
synonymous_variant | LOW | c.51C>T | p.Val17Val | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/8 | 148/3052 | 51/1275 | 17/424 | chr2 | 174398334 | |||
| chr2:174424586 | T | C | 1 | a0002c0004 | 14 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(11): Show |
synonymous_variant | LOW | c.1029T>C | p.Pro343Pro | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/8 | 1126/3052 | 1029/1275 | 343/424 | chr2 | 174424586 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:174395733 | A | T | 2 | a0001c0001t0006 a0001c0001t0018 |
6 | HG02257.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-94A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/8 | 2551 | chr2 | 174395733 | ||||||
| chr2:174428105 | G | A | 1 | a0001c0001t0011 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*210G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 210 | chr2 | 174428105 | ||||||
| chr2:174428111 | T | C | 2 | a0001c0001t0003 a0001c0001t0007 |
20 | HG00735.hp2 HG01884.hp1 HG02109.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*216T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 216 | chr2 | 174428111 | ||||||
| chr2:174428160 | G | C | 5 | a0002c0002t0002 a0002c0002t0004 a0002c0002t0012 others(2): Show |
87 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*265G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 265 | chr2 | 174428160 | ||||||
| chr2:174428196 | A | G | 1 | a0005c0007t0010 | 2 | NA18964.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*301A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 301 | chr2 | 174428196 | ||||||
| chr2:174428220 | G | T | 1 | a0001c0001t0009 | 2 | HG03704.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*325G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 325 | chr2 | 174428220 | ||||||
| chr2:174428351 | C | A | 2 | a0001c0001t0005 a0001c0001t0013 |
9 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*456C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 456 | chr2 | 174428351 | ||||||
| chr2:174428589 | G | T | 1 | a0001c0001t0013 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*694G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 694 | chr2 | 174428589 | ||||||
| chr2:174428620 | G | A | 1 | a0003c0003t0014 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*725G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 725 | chr2 | 174428620 | ||||||
| chr2:174428761 | A | G | 1 | a0001c0001t0008 | 2 | NA18979.hp2 NA19000.hp2 |
3_prime_UTR_variant | MODIFIER | c.*866A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 866 | chr2 | 174428761 | ||||||
| chr2:174428768 | T | C | 1 | a0003c0003t0015 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*873T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 873 | chr2 | 174428768 | ||||||
| chr2:174428910 | C | T | 5 | a0002c0002t0002 a0002c0002t0004 a0002c0002t0012 others(2): Show |
87 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*1015C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1015 | chr2 | 174428910 | ||||||
| chr2:174428968 | A | C | 1 | a0005c0007t0010 | 2 | NA18964.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1073A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1073 | chr2 | 174428968 | ||||||
| chr2:174429018 | A | C | 1 | a0001c0001t0018 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1123A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1123 | chr2 | 174429018 | ||||||
| chr2:174429081 | A | G | 1 | a0005c0007t0010 | 2 | NA18964.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1186A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1186 | chr2 | 174429081 | ||||||
| chr2:174429294 | C | T | 1 | a0001c0001t0007 | 2 | HG02109.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1399C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1399 | chr2 | 174429294 | ||||||
| chr2:174429319 | C | T | 1 | a0005c0007t0010 | 2 | NA18964.hp1 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1424C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1424 | chr2 | 174429319 | ||||||
| chr2:174429340 | C | T | 1 | a0002c0002t0012 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1445C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1445 | chr2 | 174429340 | ||||||
| chr2:174429351 | C | T | 1 | a0001c0001t0017 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1456C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1456 | chr2 | 174429351 | ||||||
| chr2:174429476 | G | T | 1 | a0001c0001t0016 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1581G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1581 | chr2 | 174429476 | ||||||
| chr2:174429525 | A | C | 1 | a0001c0001t0016 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1630A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1630 | chr2 | 174429525 | ||||||
| chr2:174429526 | A | G | 4 | a0002c0002t0002 a0002c0002t0012 a0002c0004t0002 others(1): Show |
70 | HG00558.hp1 HG00642.hp2 HG00673.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1631A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1631 | chr2 | 174429526 | ||||||
| chr2:174429529 | C | T | 4 | a0002c0002t0002 a0002c0002t0012 a0002c0004t0002 others(1): Show |
70 | HG00558.hp1 HG00642.hp2 HG00673.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*1634C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 8/8 | 1634 | chr2 | 174429529 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:174396181 | A | T | 29 | a0001c0001t0001g0222 a0001c0001t0003g0218 a0001c0001t0005g0057 others(26): Show |
54 | HG00558.hp1 HG00673.hp1 HG01891.hp1 others(51): Show |
intron_variant | MODIFIER | c.-10+364A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396181 | |||||||
| chr2:174396349 | G | A | 1 | a0001c0001t0003g0058 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-10+532G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396349 | |||||||
| chr2:174396420 | T | C | 52 | a0001c0001t0001g0072 a0001c0001t0001g0080 a0001c0001t0001g0222 others(49): Show |
89 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.-10+603T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396420 | |||||||
| chr2:174396569 | GGTGGATC others(4): Show |
G | 1 | a0002c0002t0002g0214 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-10+754_-10+764del others(11): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 174396569 | ||||||
| chr2:174396690 | C | G | 1 | a0003c0003t0001g0213 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-10+873C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396690 | |||||||
| chr2:174396697 | T | C | 39 | a0001c0001t0001g0222 a0001c0001t0003g0218 a0002c0002t0002g0002 others(36): Show |
73 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.-10+880T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396697 | |||||||
| chr2:174396715 | T | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(30): Show |
42 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.-10+898T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396715 | |||||||
| chr2:174396721 | G | C | 39 | a0001c0001t0001g0222 a0001c0001t0003g0218 a0002c0002t0002g0002 others(36): Show |
73 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.-10+904G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396721 | |||||||
| chr2:174396734 | G | T | 1 | a0001c0001t0001g0052 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-10+917G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396734 | |||||||
| chr2:174396796 | C | CA | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0082 others(5): Show |
11 | HG02165.hp2 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10+991dupA | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 174396796 | ||||||
| chr2:174396808 | A | AAAAAAC | 35 | a0001c0001t0001g0222 a0001c0001t0003g0218 a0002c0002t0002g0002 others(32): Show |
69 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-10+991_-10+992ins others(6): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396808 | |||||||
| chr2:174396809 | C | A | 41 | a0001c0001t0001g0222 a0001c0001t0003g0218 a0002c0002t0002g0002 others(38): Show |
75 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.-10+992C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396809 | |||||||
| chr2:174396849 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-10+1032C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174396849 | |||||||
| chr2:174397002 | G | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1185G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397002 | |||||||
| chr2:174397026 | A | G | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+1209A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397026 | |||||||
| chr2:174397204 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-9-1071T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397204 | |||||||
| chr2:174397249 | C | T | 1 | a0001c0001t0006g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-9-1026C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397249 | |||||||
| chr2:174397282 | C | T | 46 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0001t0001g0209 others(43): Show |
81 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.-9-993C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397282 | |||||||
| chr2:174397345 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-9-930G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397345 | |||||||
| chr2:174397422 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-9-853G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397422 | |||||||
| chr2:174397434 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-9-841G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397434 | |||||||
| chr2:174397457 | C | A | 1 | a0001c0001t0018g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9-818C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397457 | |||||||
| chr2:174397560 | A | G | 2 | a0002c0002t0002g0016 a0002c0002t0002g0217 |
5 | NA18954.hp2 NA18963.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9-715A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397560 | |||||||
| chr2:174397714 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.-9-561G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397714 | |||||||
| chr2:174397900 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-9-375T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397900 | |||||||
| chr2:174397950 | G | A | 44 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0001t0001g0209 others(41): Show |
79 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.-9-325G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174397950 | |||||||
| chr2:174398036 | G | A | 2 | a0001c0001t0003g0117 a0001c0001t0003g0118 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-9-239G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174398036 | |||||||
| chr2:174398072 | AAGCCCTG others(18): Show |
A | 12 | a0001c0001t0001g0080 a0002c0004t0002g0012 a0002c0004t0002g0025 others(9): Show |
15 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9-198_-9-174delCT others(23): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 174398072 | ||||||
| chr2:174398239 | G | GT | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-34dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 174398239 | ||||||
| chr2:174398242 | C | T | 43 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(40): Show |
78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.-9-33C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 1/7 | chr2 | 174398242 | |||||||
| chr2:174398490 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
131 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.159+48A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174398490 | |||||||
| chr2:174398607 | C | T | 39 | a0001c0001t0001g0206 a0001c0001t0001g0222 a0002c0002t0002g0002 others(36): Show |
73 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.159+165C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174398607 | |||||||
| chr2:174398753 | C | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(228): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.159+311C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174398753 | |||||||
| chr2:174398794 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.159+352T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174398794 | |||||||
| chr2:174398903 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.159+461G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174398903 | |||||||
| chr2:174398940 | A | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.159+498A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174398940 | |||||||
| chr2:174399004 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.159+562C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174399004 | |||||||
| chr2:174399590 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.160-332A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | chr2 | 174399590 | |||||||
| chr2:174399899 | C | CT | 33 | a0001c0001t0001g0031 a0001c0001t0001g0038 a0001c0001t0001g0080 others(30): Show |
42 | HG00733.hp2 HG00735.hp2 HG00741.hp1 others(39): Show |
splice_region_variant&intron_variant | LOW | c.160-5dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 174399899 | ||||||
| chr2:174399899 | C | CTT | 31 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(28): Show |
40 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(37): Show |
splice_region_variant&intron_variant | LOW | c.160-6_160-5dupTT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 174399899 | ||||||
| chr2:174399899 | CT | C | 25 | a0001c0001t0001g0034 a0001c0001t0001g0052 a0001c0001t0001g0132 others(22): Show |
29 | HG01109.hp1 HG01123.hp1 HG01192.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.160-5delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 174399899 | ||||||
| chr2:174399899 | CTTTT | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
splice_region_variant&intron_variant | LOW | c.160-8_160-5delTTTT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 174399899 | ||||||
| chr2:174400217 | G | A | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+114G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400217 | |||||||
| chr2:174400329 | C | G | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.341+226C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400329 | |||||||
| chr2:174400355 | T | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.341+252T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400355 | |||||||
| chr2:174400463 | A | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
130 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.341+360A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400463 | |||||||
| chr2:174400470 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.341+367A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400470 | |||||||
| chr2:174400471 | T | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0165 others(27): Show |
64 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.341+368T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400471 | |||||||
| chr2:174400486 | C | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.341+383C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400486 | |||||||
| chr2:174400681 | A | G | 2 | a0005c0007t0010g0109 a0005c0007t0010g0110 |
2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.342-309A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400681 | |||||||
| chr2:174400718 | A | G | 1 | a0001c0001t0001g0030 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.342-272A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400718 | |||||||
| chr2:174400817 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0167 |
4 | HG01192.hp2 HG01981.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-173T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400817 | |||||||
| chr2:174400884 | T | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0167 |
4 | HG01192.hp2 HG01981.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.342-106T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400884 | |||||||
| chr2:174400886 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.342-104G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400886 | |||||||
| chr2:174400938 | A | G | 46 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0001t0001g0209 others(43): Show |
81 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.342-52A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400938 | |||||||
| chr2:174400974 | T | C | 1 | a0002c0002t0004g0060 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.342-16T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 3/7 | chr2 | 174400974 | |||||||
| chr2:174401332 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.541+143A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174401332 | |||||||
| chr2:174401489 | A | AT | 4 | a0001c0001t0001g0034 a0001c0001t0001g0111 a0001c0001t0001g0132 others(1): Show |
5 | HG02280.hp2 HG02809.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.541+303dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174401489 | ||||||
| chr2:174401531 | T | C | 1 | a0001c0001t0001g0038 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.541+342T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174401531 | |||||||
| chr2:174401562 | G | A | 51 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(48): Show |
67 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.541+373G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174401562 | |||||||
| chr2:174401631 | A | C | 2 | a0001c0001t0003g0117 a0001c0001t0003g0118 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.541+442A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174401631 | |||||||
| chr2:174401796 | C | A | 10 | a0001c0001t0003g0020 a0001c0001t0003g0039 a0001c0001t0003g0040 others(7): Show |
15 | HG00735.hp2 HG01884.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.541+607C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174401796 | |||||||
| chr2:174401860 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.541+671G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174401860 | |||||||
| chr2:174402076 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.541+887A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402076 | |||||||
| chr2:174402127 | A | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.541+938A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402127 | |||||||
| chr2:174402144 | G | C | 1 | a0001c0001t0001g0052 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.541+955G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402144 | |||||||
| chr2:174402159 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
131 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.541+970T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402159 | |||||||
| chr2:174402309 | A | G | 1 | a0002c0004t0002g0079 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.541+1120A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402309 | |||||||
| chr2:174402323 | T | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.541+1134T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402323 | |||||||
| chr2:174402340 | T | C | 16 | a0002c0002t0002g0011 a0002c0002t0002g0017 a0002c0002t0002g0066 others(13): Show |
26 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.541+1151T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402340 | |||||||
| chr2:174402390 | T | G | 2 | a0001c0001t0001g0042 a0010c0009t0001g0168 |
3 | NA18952.hp2 NA18993.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.541+1201T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402390 | |||||||
| chr2:174402666 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.542-1437G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402666 | |||||||
| chr2:174402717 | G | A | 1 | a0001c0001t0006g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.542-1386G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174402717 | |||||||
| chr2:174402821 | A | AT | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.542-1277dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174402821 | ||||||
| chr2:174403084 | G | GT | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(71): Show |
128 | HG00140.hp2 HG00558.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.542-1018dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174403084 | ||||||
| chr2:174403085 | T | TAA | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.542-1006_542-1005d others(4): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174403085 | ||||||
| chr2:174403085 | TA | T | 37 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(34): Show |
71 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.542-1005delA | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174403085 | ||||||
| chr2:174403086 | A | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0169 a0001c0001t0001g0170 |
4 | HG00280.hp2 HG02698.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-1017A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403086 | |||||||
| chr2:174403138 | C | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(23): Show |
35 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.542-965C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403138 | |||||||
| chr2:174403148 | G | T | 2 | a0002c0004t0002g0071 a0002c0004t0002g0081 |
2 | HG02735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.542-955G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403148 | |||||||
| chr2:174403315 | A | C | 1 | a0008c0012t0001g0201 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.542-788A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403315 | |||||||
| chr2:174403527 | C | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.542-576C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403527 | |||||||
| chr2:174403528 | CAATAAA | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.542-569_542-564del others(6): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174403528 | ||||||
| chr2:174403569 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0203 |
2 | NA18983.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.542-534T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403569 | |||||||
| chr2:174403606 | C | T | 43 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(40): Show |
78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.542-497C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403606 | |||||||
| chr2:174403716 | G | A | 2 | a0005c0007t0010g0109 a0005c0007t0010g0110 |
2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.542-387G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403716 | |||||||
| chr2:174403743 | G | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.542-360G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403743 | |||||||
| chr2:174403882 | AT | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.542-214delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 174403882 | ||||||
| chr2:174403976 | C | G | 1 | a0001c0001t0001g0029 | 2 | HG00140.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.542-127C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174403976 | |||||||
| chr2:174404035 | A | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.542-68A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 4/7 | chr2 | 174404035 | |||||||
| chr2:174404329 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.754+14A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404329 | |||||||
| chr2:174404458 | A | T | 2 | a0005c0007t0010g0109 a0005c0007t0010g0110 |
2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.754+143A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404458 | |||||||
| chr2:174404563 | G | A | 2 | a0005c0007t0010g0109 a0005c0007t0010g0110 |
2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.754+248G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404563 | |||||||
| chr2:174404590 | A | G | 1 | a0001c0001t0003g0218 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.754+275A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404590 | |||||||
| chr2:174404608 | C | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+293C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404608 | |||||||
| chr2:174404725 | C | T | 4 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
4 | HG02109.hp2 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754+410C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404725 | |||||||
| chr2:174404919 | C | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+604C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404919 | |||||||
| chr2:174404919 | C | G | 5 | a0001c0001t0001g0199 a0001c0005t0001g0157 a0001c0005t0001g0158 others(2): Show |
5 | HG01891.hp2 HG02622.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+604C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404919 | |||||||
| chr2:174404941 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+626G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174404941 | |||||||
| chr2:174405015 | C | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+700C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405015 | |||||||
| chr2:174405018 | T | C | 1 | a0001c0001t0001g0034 | 2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.754+703T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405018 | |||||||
| chr2:174405026 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0133 a0001c0001t0001g0200 |
3 | HG02717.hp1 HG02809.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.754+711T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405026 | |||||||
| chr2:174405026 | T | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+711T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405026 | |||||||
| chr2:174405071 | C | T | 2 | a0001c0001t0007g0155 a0001c0001t0007g0156 |
2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.754+756C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405071 | |||||||
| chr2:174405314 | T | C | 7 | a0001c0001t0001g0052 a0001c0001t0001g0116 a0001c0001t0001g0209 others(4): Show |
8 | HG02109.hp2 HG02132.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+999T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405314 | |||||||
| chr2:174405322 | C | A | 7 | a0001c0001t0001g0052 a0001c0001t0001g0116 a0001c0001t0001g0209 others(4): Show |
8 | HG02109.hp2 HG02132.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+1007C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405322 | |||||||
| chr2:174405597 | A | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+1282A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405597 | |||||||
| chr2:174405604 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+1289G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405604 | |||||||
| chr2:174405631 | T | C | 2 | a0001c0001t0007g0155 a0001c0001t0007g0156 |
2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.754+1316T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405631 | |||||||
| chr2:174405634 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.754+1319A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405634 | |||||||
| chr2:174405838 | C | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+1523C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405838 | |||||||
| chr2:174405888 | G | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(29): Show |
41 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.754+1573G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405888 | |||||||
| chr2:174405934 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+1619G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405934 | |||||||
| chr2:174405991 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.754+1676G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174405991 | |||||||
| chr2:174406066 | A | G | 43 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(40): Show |
78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.754+1751A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406066 | |||||||
| chr2:174406088 | A | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+1773A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406088 | |||||||
| chr2:174406197 | G | A | 12 | a0001c0001t0001g0080 a0002c0004t0002g0012 a0002c0004t0002g0025 others(9): Show |
15 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.754+1882G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406197 | |||||||
| chr2:174406267 | A | G | 33 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(30): Show |
42 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.754+1952A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406267 | |||||||
| chr2:174406294 | G | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+1979G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406294 | |||||||
| chr2:174406333 | G | T | 8 | a0001c0001t0005g0057 a0001c0001t0005g0145 a0001c0001t0005g0228 others(5): Show |
9 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.754+2018G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406333 | |||||||
| chr2:174406383 | A | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(24): Show |
36 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.754+2068A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406383 | |||||||
| chr2:174406384 | T | A | 27 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(24): Show |
36 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.754+2069T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406384 | |||||||
| chr2:174406396 | G | A | 30 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(27): Show |
39 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.754+2081G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406396 | |||||||
| chr2:174406417 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+2102G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406417 | |||||||
| chr2:174406508 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.754+2193G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406508 | |||||||
| chr2:174406511 | C | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+2196C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406511 | |||||||
| chr2:174406543 | C | A | 2 | a0001c0001t0007g0155 a0001c0001t0007g0156 |
2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.754+2228C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406543 | |||||||
| chr2:174406549 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.754+2234A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406549 | |||||||
| chr2:174406656 | G | T | 43 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(40): Show |
78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.754+2341G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406656 | |||||||
| chr2:174406702 | C | A | 44 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0001t0001g0209 others(41): Show |
79 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.754+2387C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406702 | |||||||
| chr2:174406821 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+2506G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406821 | |||||||
| chr2:174406860 | A | C | 43 | a0001c0001t0001g0222 a0001c0001t0003g0058 a0001c0001t0003g0117 others(40): Show |
77 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.754+2545A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406860 | |||||||
| chr2:174406911 | T | G | 21 | a0001c0001t0001g0162 a0003c0003t0001g0004 a0003c0003t0001g0019 others(18): Show |
30 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.754+2596T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406911 | |||||||
| chr2:174406943 | A | G | 51 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(48): Show |
67 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.754+2628A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174406943 | |||||||
| chr2:174407044 | C | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+2729C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407044 | |||||||
| chr2:174407085 | G | C | 59 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(56): Show |
75 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.754+2770G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407085 | |||||||
| chr2:174407101 | G | T | 1 | a0001c0001t0001g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.754+2786G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407101 | |||||||
| chr2:174407175 | A | G | 1 | a0001c0001t0006g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.754+2860A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407175 | |||||||
| chr2:174407300 | G | A | 5 | a0001c0001t0001g0038 a0001c0005t0001g0157 a0001c0005t0001g0158 others(2): Show |
6 | HG01891.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.754+2985G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407300 | |||||||
| chr2:174407376 | G | A | 1 | a0009c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.754+3061G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407376 | |||||||
| chr2:174407584 | C | T | 1 | a0002c0002t0004g0070 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.754+3269C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407584 | |||||||
| chr2:174407665 | C | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0051 others(3): Show |
9 | HG02523.hp2 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.754+3350C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407665 | |||||||
| chr2:174407703 | TC | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+3389delC | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407703 | |||||||
| chr2:174407709 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.754+3394C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407709 | |||||||
| chr2:174407765 | C | T | 1 | a0001c0001t0005g0233 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.754+3450C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407765 | |||||||
| chr2:174407770 | TTGAGTGG others(12): Show |
T | 1 | a0001c0001t0001g0103 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.754+3461_754+3479d others(21): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174407770 | ||||||
| chr2:174407777 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0170 |
2 | NA18939.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.754+3462G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407777 | |||||||
| chr2:174407780 | T | A | 1 | a0001c0001t0018g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.754+3465T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407780 | |||||||
| chr2:174407880 | G | C | 2 | a0005c0007t0010g0109 a0005c0007t0010g0110 |
2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.754+3565G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407880 | |||||||
| chr2:174407977 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.754+3662C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174407977 | |||||||
| chr2:174408032 | A | G | 156 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(153): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.754+3717A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408032 | |||||||
| chr2:174408116 | A | G | 6 | a0002c0002t0002g0010 a0002c0002t0002g0016 a0002c0002t0002g0056 others(3): Show |
14 | HG02080.hp2 HG02523.hp1 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.754+3801A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408116 | |||||||
| chr2:174408163 | A | G | 1 | a0001c0001t0001g0170 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.754+3848A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408163 | |||||||
| chr2:174408362 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+4047G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408362 | |||||||
| chr2:174408406 | C | CTT | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+4092_754+4093i others(4): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174408406 | ||||||
| chr2:174408457 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0119 |
3 | HG02055.hp1 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.754+4142T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408457 | |||||||
| chr2:174408488 | T | C | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+4173T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408488 | |||||||
| chr2:174408525 | C | T | 1 | a0002c0002t0002g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.754+4210C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408525 | |||||||
| chr2:174408554 | C | T | 1 | a0002c0002t0002g0226 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.754+4239C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408554 | |||||||
| chr2:174408556 | G | A | 1 | a0001c0001t0006g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.754+4241G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408556 | |||||||
| chr2:174408588 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+4273G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408588 | |||||||
| chr2:174408598 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0091 |
3 | HG02258.hp2 HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.754+4283G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408598 | |||||||
| chr2:174408610 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.754+4295C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408610 | |||||||
| chr2:174408620 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.754+4305C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408620 | |||||||
| chr2:174408621 | G | A | 58 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(55): Show |
74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.754+4306G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408621 | |||||||
| chr2:174408635 | C | A | 1 | a0003c0003t0015g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.754+4320C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408635 | |||||||
| chr2:174408640 | T | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+4325T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408640 | |||||||
| chr2:174408663 | A | G | 1 | a0002c0004t0002g0025 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.754+4348A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408663 | |||||||
| chr2:174408678 | T | G | 1 | a0001c0001t0001g0206 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.754+4363T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408678 | |||||||
| chr2:174408693 | T | G | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+4378T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408693 | |||||||
| chr2:174408698 | T | A | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+4383T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408698 | |||||||
| chr2:174408715 | T | C | 3 | a0001c0001t0001g0204 a0004c0006t0001g0022 a0006c0011t0001g0175 |
5 | HG00738.hp1 HG01496.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+4400T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408715 | |||||||
| chr2:174408763 | G | C | 4 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
4 | HG02630.hp1 HG03225.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.754+4448G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408763 | |||||||
| chr2:174408777 | A | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+4462A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408777 | |||||||
| chr2:174408809 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(63): Show |
115 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.754+4494G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408809 | |||||||
| chr2:174408818 | C | T | 71 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0036 others(68): Show |
93 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.754+4503C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408818 | |||||||
| chr2:174408819 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+4504G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408819 | |||||||
| chr2:174408858 | G | A | 1 | a0001c0001t0005g0228 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.754+4543G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408858 | |||||||
| chr2:174408863 | C | T | 8 | a0001c0001t0003g0020 a0001c0001t0003g0039 a0001c0001t0003g0040 others(5): Show |
13 | HG00735.hp2 HG01884.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.754+4548C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408863 | |||||||
| chr2:174408864 | C | T | 1 | a0003c0003t0001g0131 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.754+4549C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408864 | |||||||
| chr2:174408936 | C | G | 1 | a0001c0001t0003g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.754+4621C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408936 | |||||||
| chr2:174408953 | C | T | 39 | a0001c0001t0001g0102 a0001c0001t0001g0222 a0002c0002t0002g0002 others(36): Show |
73 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.754+4638C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174408953 | |||||||
| chr2:174409096 | C | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+4781C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409096 | |||||||
| chr2:174409191 | C | T | 1 | a0001c0001t0001g0013 | 4 | NA19005.hp1 NA19010.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.754+4876C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409191 | |||||||
| chr2:174409249 | G | A | 47 | a0001c0001t0001g0052 a0001c0001t0001g0120 a0001c0001t0001g0207 others(44): Show |
82 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.754+4934G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409249 | |||||||
| chr2:174409251 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.754+4936C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409251 | |||||||
| chr2:174409252 | G | A | 4 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
4 | HG02109.hp2 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754+4937G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409252 | |||||||
| chr2:174409260 | A | C | 2 | a0005c0007t0010g0109 a0005c0007t0010g0110 |
2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.754+4945A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409260 | |||||||
| chr2:174409321 | C | A | 15 | a0001c0001t0001g0080 a0001c0001t0001g0178 a0002c0004t0002g0012 others(12): Show |
18 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.754+5006C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409321 | |||||||
| chr2:174409321 | C | T | 1 | a0001c0005t0001g0160 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.754+5006C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409321 | |||||||
| chr2:174409322 | G | A | 21 | a0001c0001t0001g0162 a0003c0003t0001g0004 a0003c0003t0001g0019 others(18): Show |
30 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.754+5007G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409322 | |||||||
| chr2:174409434 | C | T | 2 | a0002c0004t0002g0077 a0002c0004t0002g0078 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.754+5119C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409434 | |||||||
| chr2:174409460 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.754+5145G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409460 | |||||||
| chr2:174409469 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.754+5154A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409469 | |||||||
| chr2:174409525 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.754+5210G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409525 | |||||||
| chr2:174409692 | C | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0143 others(1): Show |
6 | HG02615.hp2 HG02622.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.754+5377C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409692 | |||||||
| chr2:174409741 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.754+5426G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409741 | |||||||
| chr2:174409747 | A | G | 7 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0050 others(4): Show |
10 | HG02165.hp1 HG02615.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.754+5432A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409747 | |||||||
| chr2:174409770 | C | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+5455C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409770 | |||||||
| chr2:174409800 | C | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+5485C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409800 | |||||||
| chr2:174409813 | G | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+5498G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409813 | |||||||
| chr2:174409890 | T | C | 48 | a0001c0001t0001g0222 a0001c0001t0003g0020 a0001c0001t0003g0039 others(45): Show |
87 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.754+5575T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409890 | |||||||
| chr2:174409916 | G | C | 2 | a0001c0001t0001g0111 a0007c0010t0001g0148 |
2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.754+5601G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174409916 | |||||||
| chr2:174409960 | GC | G | 8 | a0001c0001t0005g0057 a0001c0001t0005g0145 a0001c0001t0005g0228 others(5): Show |
9 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.754+5647delC | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174409960 | ||||||
| chr2:174409999 | T | TC | 2 | a0001c0001t0003g0039 a0001c0001t0003g0040 |
4 | HG02280.hp1 HG03486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.754+5687dupC | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174409999 | ||||||
| chr2:174410003 | G | A | 8 | a0001c0001t0005g0057 a0001c0001t0005g0145 a0001c0001t0005g0228 others(5): Show |
9 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.754+5688G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410003 | |||||||
| chr2:174410022 | G | T | 9 | a0001c0001t0001g0163 a0001c0001t0005g0057 a0001c0001t0005g0145 others(6): Show |
10 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.754+5707G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410022 | |||||||
| chr2:174410023 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.754+5708C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410023 | |||||||
| chr2:174410043 | T | C | 3 | a0001c0001t0001g0180 a0001c0001t0001g0211 a0002c0004t0002g0025 |
4 | HG03491.hp2 HG03492.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.754+5728T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410043 | |||||||
| chr2:174410048 | C | G | 16 | a0002c0002t0002g0011 a0002c0002t0002g0017 a0002c0002t0002g0066 others(13): Show |
26 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.754+5733C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410048 | |||||||
| chr2:174410061 | G | A | 1 | a0009c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.754+5746G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410061 | |||||||
| chr2:174410089 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0112 others(1): Show |
6 | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+5774C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410089 | |||||||
| chr2:174410129 | C | T | 3 | a0001c0001t0003g0058 a0001c0001t0003g0117 a0001c0001t0003g0118 |
3 | HG02965.hp1 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.754+5814C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410129 | |||||||
| chr2:174410172 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.754+5857T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410172 | |||||||
| chr2:174410179 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.754+5864C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410179 | |||||||
| chr2:174410180 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.754+5865G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410180 | |||||||
| chr2:174410192 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.754+5877G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410192 | |||||||
| chr2:174410216 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.754+5901G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410216 | |||||||
| chr2:174410229 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.754+5914C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410229 | |||||||
| chr2:174410273 | C | T | 1 | a0002c0002t0002g0225 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.754+5958C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410273 | |||||||
| chr2:174410279 | C | T | 38 | a0001c0001t0001g0200 a0001c0001t0001g0222 a0002c0002t0002g0002 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+5964C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410279 | |||||||
| chr2:174410315 | G | T | 2 | a0005c0007t0010g0109 a0005c0007t0010g0110 |
2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.754+6000G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410315 | |||||||
| chr2:174410318 | C | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+6003C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410318 | |||||||
| chr2:174410319 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.754+6004G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410319 | |||||||
| chr2:174410321 | G | A | 1 | a0002c0002t0002g0220 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.754+6006G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410321 | |||||||
| chr2:174410334 | T | A | 156 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(153): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.754+6019T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410334 | |||||||
| chr2:174410352 | A | C | 1 | a0001c0001t0003g0153 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.754+6037A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410352 | |||||||
| chr2:174410371 | T | C | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+6056T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410371 | |||||||
| chr2:174410382 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.754+6067C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410382 | |||||||
| chr2:174410388 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.754+6073C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410388 | |||||||
| chr2:174410504 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+6189G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410504 | |||||||
| chr2:174410549 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.754+6234C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410549 | |||||||
| chr2:174410919 | G | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+6604G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410919 | |||||||
| chr2:174410923 | G | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+6608G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410923 | |||||||
| chr2:174410951 | C | T | 51 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(48): Show |
67 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.754+6636C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410951 | |||||||
| chr2:174410959 | C | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+6644C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410959 | |||||||
| chr2:174410983 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.754+6668T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410983 | |||||||
| chr2:174410993 | C | T | 5 | a0003c0003t0001g0035 a0003c0003t0001g0138 a0003c0003t0001g0139 others(2): Show |
6 | HG01069.hp1 HG01070.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.754+6678C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174410993 | |||||||
| chr2:174411123 | A | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+6808A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411123 | |||||||
| chr2:174411156 | C | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+6841C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411156 | |||||||
| chr2:174411350 | TG | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+7036delG | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411350 | |||||||
| chr2:174411547 | C | T | 2 | a0001c0005t0001g0158 a0001c0005t0001g0159 |
2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.754+7232C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411547 | |||||||
| chr2:174411601 | G | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+7286G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411601 | |||||||
| chr2:174411605 | A | T | 1 | a0001c0001t0001g0167 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.754+7290A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411605 | |||||||
| chr2:174411609 | C | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+7294C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411609 | |||||||
| chr2:174411642 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.754+7327C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411642 | |||||||
| chr2:174411702 | A | T | 1 | a0001c0001t0003g0152 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.754+7387A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411702 | |||||||
| chr2:174411795 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.754+7480C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411795 | |||||||
| chr2:174411836 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.754+7521G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411836 | |||||||
| chr2:174411896 | G | C | 4 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(1): Show |
4 | HG02109.hp2 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754+7581G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411896 | |||||||
| chr2:174411901 | T | G | 46 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0001t0001g0209 others(43): Show |
81 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.754+7586T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411901 | |||||||
| chr2:174411921 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.754+7606A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411921 | |||||||
| chr2:174411928 | A | T | 43 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(40): Show |
78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.754+7613A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411928 | |||||||
| chr2:174411935 | T | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(231): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.754+7620T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411935 | |||||||
| chr2:174411999 | G | A | 43 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(40): Show |
78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.754+7684G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174411999 | |||||||
| chr2:174412007 | T | C | 1 | a0001c0001t0001g0027 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.754+7692T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412007 | |||||||
| chr2:174412086 | G | T | 46 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0001t0001g0209 others(43): Show |
81 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.754+7771G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412086 | |||||||
| chr2:174412124 | C | CA | 41 | a0001c0001t0001g0044 a0001c0001t0001g0222 a0002c0002t0002g0002 others(38): Show |
76 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.754+7819dupA | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174412124 | ||||||
| chr2:174412178 | T | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0092 a0001c0001t0001g0101 |
4 | HG03704.hp2 HG03834.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.754+7863T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412178 | |||||||
| chr2:174412242 | G | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0142 others(2): Show |
7 | HG02615.hp2 HG02622.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.754+7927G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412242 | |||||||
| chr2:174412351 | A | AT | 36 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0162 others(33): Show |
56 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.754+8050dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174412351 | ||||||
| chr2:174412351 | A | T | 6 | a0001c0001t0005g0057 a0001c0001t0005g0228 a0001c0001t0005g0230 others(3): Show |
7 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.754+8036A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412351 | |||||||
| chr2:174412365 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.754+8050T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412365 | |||||||
| chr2:174412499 | AT | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+8185delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412499 | |||||||
| chr2:174412517 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0166 |
3 | NA18965.hp1 NA18981.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.754+8202C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412517 | |||||||
| chr2:174412679 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.754+8364A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412679 | |||||||
| chr2:174412824 | C | T | 17 | a0002c0002t0002g0011 a0002c0002t0002g0017 a0002c0002t0002g0059 others(14): Show |
27 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.754+8509C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412824 | |||||||
| chr2:174412860 | C | CT | 37 | a0001c0001t0001g0015 a0001c0001t0001g0048 a0001c0001t0001g0049 others(34): Show |
71 | HG00323.hp2 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.754+8569dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174412860 | ||||||
| chr2:174412860 | C | CTT | 7 | a0002c0002t0002g0023 a0002c0002t0002g0054 a0002c0002t0002g0066 others(4): Show |
10 | HG00642.hp2 HG00673.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.754+8568_754+8569d others(4): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174412860 | ||||||
| chr2:174412860 | CT | C | 110 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(107): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.754+8569delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174412860 | ||||||
| chr2:174412891 | G | A | 58 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(55): Show |
74 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.754+8576G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412891 | |||||||
| chr2:174412931 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.754+8616G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412931 | |||||||
| chr2:174412962 | G | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0021 others(9): Show |
29 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.754+8647G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412962 | |||||||
| chr2:174412963 | G | C | 1 | a0003c0003t0001g0134 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.754+8648G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412963 | |||||||
| chr2:174412988 | A | C | 155 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.754+8673A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174412988 | |||||||
| chr2:174413043 | A | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+8728A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413043 | |||||||
| chr2:174413100 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.754+8785G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413100 | |||||||
| chr2:174413123 | C | T | 10 | a0002c0002t0004g0006 a0002c0002t0004g0024 a0002c0002t0004g0060 others(7): Show |
16 | HG00323.hp2 HG00639.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.754+8808C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413123 | |||||||
| chr2:174413150 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.754+8835G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413150 | |||||||
| chr2:174413159 | A | T | 2 | a0001c0001t0003g0117 a0001c0001t0003g0118 |
2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.754+8844A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413159 | |||||||
| chr2:174413162 | A | G | 155 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.754+8847A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413162 | |||||||
| chr2:174413172 | G | A | 29 | a0001c0001t0001g0162 a0001c0001t0005g0057 a0001c0001t0005g0145 others(26): Show |
39 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.754+8857G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413172 | |||||||
| chr2:174413384 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.754+9069A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413384 | |||||||
| chr2:174413569 | CT | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.754+9263delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174413569 | ||||||
| chr2:174413586 | C | CT | 21 | a0001c0001t0001g0031 a0001c0001t0001g0038 a0001c0001t0001g0084 others(18): Show |
24 | HG01175.hp1 HG01175.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.755-9277dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174413586 | ||||||
| chr2:174413586 | CT | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
202 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.755-9277delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174413586 | ||||||
| chr2:174413586 | CTTTTTTT others(7): Show |
C | 6 | a0001c0001t0003g0020 a0001c0001t0003g0041 a0001c0001t0003g0150 others(3): Show |
9 | HG00735.hp2 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.754+9280_755-9277d others(16): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174413586 | ||||||
| chr2:174413653 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0165 |
8 | HG00642.hp1 HG01258.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-9232C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413653 | |||||||
| chr2:174413654 | G | A | 1 | a0002c0002t0002g0214 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.755-9231G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413654 | |||||||
| chr2:174413830 | T | A | 43 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(40): Show |
78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.755-9055T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413830 | |||||||
| chr2:174413880 | C | T | 1 | a0001c0001t0005g0231 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.755-9005C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174413880 | |||||||
| chr2:174414119 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.755-8766T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414119 | |||||||
| chr2:174414137 | TC | T | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.755-8745delC | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174414137 | ||||||
| chr2:174414175 | T | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-8710T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414175 | |||||||
| chr2:174414321 | C | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(23): Show |
35 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.755-8564C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414321 | |||||||
| chr2:174414502 | A | G | 15 | a0001c0001t0003g0020 a0001c0001t0003g0039 a0001c0001t0003g0040 others(12): Show |
20 | HG00735.hp2 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.755-8383A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414502 | |||||||
| chr2:174414638 | T | C | 10 | a0001c0001t0003g0020 a0001c0001t0003g0039 a0001c0001t0003g0040 others(7): Show |
15 | HG00735.hp2 HG01884.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.755-8247T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414638 | |||||||
| chr2:174414657 | A | G | 7 | a0001c0001t0005g0057 a0001c0001t0005g0228 a0001c0001t0005g0230 others(4): Show |
8 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-8228A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414657 | |||||||
| chr2:174414765 | C | CT | 127 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(124): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.755-8104dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174414765 | ||||||
| chr2:174414765 | C | T | 2 | a0005c0007t0010g0109 a0005c0007t0010g0110 |
2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.755-8120C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414765 | |||||||
| chr2:174414910 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.755-7975C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414910 | |||||||
| chr2:174414963 | G | A | 43 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(40): Show |
78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.755-7922G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174414963 | |||||||
| chr2:174415143 | T | C | 5 | a0002c0002t0004g0061 a0002c0002t0004g0063 a0002c0002t0004g0064 others(2): Show |
5 | HG00323.hp2 HG02698.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.755-7742T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415143 | |||||||
| chr2:174415194 | A | G | 1 | a0001c0001t0018g0083 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.755-7691A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415194 | |||||||
| chr2:174415254 | AT | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-7623delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174415254 | ||||||
| chr2:174415297 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0132 |
3 | HG02280.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.755-7588T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415297 | |||||||
| chr2:174415386 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.755-7499A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415386 | |||||||
| chr2:174415552 | A | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02630.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.755-7333A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415552 | |||||||
| chr2:174415590 | A | T | 1 | a0001c0001t0003g0041 | 2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.755-7295A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415590 | |||||||
| chr2:174415606 | T | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-7279T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415606 | |||||||
| chr2:174415643 | G | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-7242G>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415643 | |||||||
| chr2:174415671 | G | A | 1 | a0001c0001t0013g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.755-7214G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415671 | |||||||
| chr2:174415675 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.755-7210C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415675 | |||||||
| chr2:174415770 | A | G | 46 | a0001c0001t0001g0052 a0001c0001t0001g0207 a0001c0001t0001g0209 others(43): Show |
81 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.755-7115A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415770 | |||||||
| chr2:174415914 | A | G | 43 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(40): Show |
78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.755-6971A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415914 | |||||||
| chr2:174415965 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.755-6920G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174415965 | |||||||
| chr2:174416094 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.755-6791A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416094 | |||||||
| chr2:174416256 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.755-6629G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416256 | |||||||
| chr2:174416320 | A | T | 1 | a0002c0002t0002g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.755-6565A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416320 | |||||||
| chr2:174416334 | A | G | 1 | a0001c0001t0001g0052 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.755-6551A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416334 | |||||||
| chr2:174416642 | G | T | 3 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0197 |
3 | NA18954.hp1 NA18991.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.755-6243G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416642 | |||||||
| chr2:174416653 | T | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-6232T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416653 | |||||||
| chr2:174416659 | A | G | 1 | a0001c0001t0001g0014 | 4 | HG00558.hp2 NA18950.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.755-6226A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416659 | |||||||
| chr2:174416668 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.755-6217A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416668 | |||||||
| chr2:174416740 | T | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
12 | HG00733.hp1 HG01346.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.755-6145T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416740 | |||||||
| chr2:174416755 | T | G | 2 | a0002c0002t0002g0053 a0002c0002t0002g0221 |
3 | NA18974.hp2 NA19062.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.755-6130T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416755 | |||||||
| chr2:174416757 | C | T | 1 | a0002c0004t0002g0079 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.755-6128C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416757 | |||||||
| chr2:174416850 | G | A | 8 | a0001c0001t0005g0057 a0001c0001t0005g0145 a0001c0001t0005g0228 others(5): Show |
9 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.755-6035G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174416850 | |||||||
| chr2:174417229 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.755-5656C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417229 | |||||||
| chr2:174417272 | C | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-5613C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417272 | |||||||
| chr2:174417375 | T | A | 1 | a0003c0003t0001g0135 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.755-5510T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417375 | |||||||
| chr2:174417436 | T | C | 43 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(40): Show |
78 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.755-5449T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417436 | |||||||
| chr2:174417577 | T | G | 4 | a0001c0005t0001g0157 a0001c0005t0001g0158 a0001c0005t0001g0159 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.755-5308T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417577 | |||||||
| chr2:174417635 | C | T | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-5250C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417635 | |||||||
| chr2:174417682 | C | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0046 a0001c0001t0001g0190 |
7 | HG00558.hp2 NA18948.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.755-5203C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417682 | |||||||
| chr2:174417825 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.755-5060C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417825 | |||||||
| chr2:174417980 | A | G | 1 | a0003c0003t0001g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.755-4905A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174417980 | |||||||
| chr2:174418008 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(196): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.755-4877T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174418008 | |||||||
| chr2:174418169 | T | C | 1 | a0004c0006t0001g0022 | 3 | HG00738.hp1 HG01496.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.755-4716T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174418169 | |||||||
| chr2:174418241 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.755-4644A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174418241 | |||||||
| chr2:174418322 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-4563G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174418322 | |||||||
| chr2:174418411 | G | T | 19 | a0001c0001t0001g0031 a0001c0001t0001g0112 a0001c0001t0001g0154 others(16): Show |
25 | HG00735.hp2 HG01884.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.755-4474G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174418411 | |||||||
| chr2:174419011 | T | C | 1 | a0001c0001t0001g0026 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.755-3874T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419011 | |||||||
| chr2:174419086 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.755-3799G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419086 | |||||||
| chr2:174419328 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.755-3557T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419328 | |||||||
| chr2:174419432 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.755-3453T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419432 | |||||||
| chr2:174419493 | C | T | 2 | a0005c0007t0010g0109 a0005c0007t0010g0110 |
2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.755-3392C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419493 | |||||||
| chr2:174419539 | C | G | 1 | a0001c0001t0001g0052 | 2 | HG02258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.755-3346C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419539 | |||||||
| chr2:174419543 | C | A | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.755-3342C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419543 | |||||||
| chr2:174419572 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG02630.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.755-3313G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419572 | |||||||
| chr2:174419586 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.755-3299G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419586 | |||||||
| chr2:174419612 | CTCACAGT others(1): Show |
C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-3269_755-3262d others(10): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174419612 | ||||||
| chr2:174419621 | T | C | 1 | a0002c0002t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.755-3264T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419621 | |||||||
| chr2:174419740 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.755-3145C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419740 | |||||||
| chr2:174419841 | G | A | 1 | a0008c0012t0001g0201 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.755-3044G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419841 | |||||||
| chr2:174419842 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.755-3043G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419842 | |||||||
| chr2:174419969 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0091 |
3 | HG02258.hp2 HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.755-2916A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174419969 | |||||||
| chr2:174420173 | AT | A | 155 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.755-2703delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174420173 | ||||||
| chr2:174420178 | T | C | 1 | a0009c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755-2707T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420178 | |||||||
| chr2:174420230 | C | T | 1 | a0009c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755-2655C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420230 | |||||||
| chr2:174420231 | G | A | 1 | a0001c0001t0013g0229 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.755-2654G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420231 | |||||||
| chr2:174420396 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0132 |
3 | HG02280.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.755-2489C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420396 | |||||||
| chr2:174420397 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.755-2488G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420397 | |||||||
| chr2:174420567 | A | G | 1 | a0009c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.755-2318A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420567 | |||||||
| chr2:174420729 | A | G | 1 | a0003c0003t0001g0137 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.755-2156A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420729 | |||||||
| chr2:174420749 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0100 |
3 | HG00280.hp1 HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.755-2136G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174420749 | |||||||
| chr2:174421041 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0176 |
7 | NA18945.hp2 NA19002.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.755-1844G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421041 | |||||||
| chr2:174421142 | G | T | 2 | a0005c0007t0010g0109 a0005c0007t0010g0110 |
2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.755-1743G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421142 | |||||||
| chr2:174421143 | A | C | 109 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(106): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.755-1742A>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421143 | |||||||
| chr2:174421251 | A | G | 112 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(109): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.755-1634A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421251 | |||||||
| chr2:174421255 | A | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-1630A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421255 | |||||||
| chr2:174421334 | T | C | 7 | a0001c0001t0005g0057 a0001c0001t0005g0228 a0001c0001t0005g0230 others(4): Show |
8 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-1551T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421334 | |||||||
| chr2:174421519 | A | G | 1 | a0005c0007t0010g0110 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.755-1366A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421519 | |||||||
| chr2:174421880 | C | T | 12 | a0001c0001t0001g0080 a0002c0004t0002g0012 a0002c0004t0002g0025 others(9): Show |
15 | HG00733.hp2 HG00735.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.755-1005C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421880 | |||||||
| chr2:174421957 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-928G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174421957 | |||||||
| chr2:174422215 | C | T | 1 | a0001c0001t0006g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.755-670C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422215 | |||||||
| chr2:174422247 | A | G | 155 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(152): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.755-638A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422247 | |||||||
| chr2:174422321 | C | G | 1 | a0001c0001t0001g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.755-564C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422321 | |||||||
| chr2:174422454 | G | A | 5 | a0001c0001t0001g0052 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.755-431G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422454 | |||||||
| chr2:174422468 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0097 |
2 | HG01099.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.755-417G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422468 | |||||||
| chr2:174422528 | T | C | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-357T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422528 | |||||||
| chr2:174422538 | C | T | 1 | a0002c0002t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.755-347C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422538 | |||||||
| chr2:174422555 | A | G | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-330A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | chr2 | 174422555 | |||||||
| chr2:174422569 | C | CA | 36 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(33): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.755-298dupA | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174422569 | ||||||
| chr2:174422569 | CA | C | 25 | a0001c0001t0001g0147 a0001c0001t0001g0198 a0001c0001t0001g0207 others(22): Show |
36 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.755-298delA | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174422569 | ||||||
| chr2:174422646 | AT | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.755-232delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 174422646 | ||||||
| chr2:174423050 | G | A | 38 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(35): Show |
72 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(69): Show |
splice_region_variant&intron_variant | LOW | c.917+3G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423050 | |||||||
| chr2:174423279 | G | A | 6 | a0001c0001t0005g0057 a0001c0001t0005g0228 a0001c0001t0005g0230 others(3): Show |
7 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.917+232G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423279 | |||||||
| chr2:174423281 | A | T | 34 | a0001c0001t0001g0222 a0002c0002t0002g0002 a0002c0002t0002g0010 others(31): Show |
66 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.917+234A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423281 | |||||||
| chr2:174423500 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(71): Show |
128 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.917+453C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423500 | |||||||
| chr2:174423501 | G | A | 1 | a0003c0003t0014g0136 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.917+454G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423501 | |||||||
| chr2:174423612 | T | C | 17 | a0002c0002t0002g0011 a0002c0002t0002g0017 a0002c0002t0002g0066 others(14): Show |
27 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.917+565T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423612 | |||||||
| chr2:174423663 | G | T | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.917+616G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423663 | |||||||
| chr2:174423761 | A | G | 1 | a0001c0001t0005g0145 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.917+714A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423761 | |||||||
| chr2:174423764 | C | T | 2 | a0003c0003t0001g0138 a0003c0003t0001g0140 |
2 | HG01069.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.918-711C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423764 | |||||||
| chr2:174423777 | C | CT | 28 | a0001c0001t0001g0034 a0001c0001t0001g0098 a0001c0001t0001g0122 others(25): Show |
32 | HG00735.hp2 HG00741.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.918-672dupT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 174423777 | ||||||
| chr2:174423777 | C | CTT | 14 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0112 others(11): Show |
19 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.918-673_918-672dup others(2): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 174423777 | ||||||
| chr2:174423777 | CT | C | 18 | a0001c0001t0001g0104 a0001c0001t0001g0178 a0001c0001t0001g0207 others(15): Show |
32 | HG00558.hp1 HG00673.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.918-672delT | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 174423777 | ||||||
| chr2:174423777 | CTT | C | 17 | a0002c0002t0002g0011 a0002c0002t0002g0017 a0002c0002t0002g0059 others(14): Show |
27 | HG00323.hp2 HG00639.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.918-673_918-672del others(2): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 174423777 | ||||||
| chr2:174423777 | CTTT | C | 10 | a0002c0002t0002g0066 a0002c0004t0002g0012 a0002c0004t0002g0025 others(7): Show |
13 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.918-674_918-672del others(3): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 174423777 | ||||||
| chr2:174423779 | T | TC | 4 | a0001c0001t0001g0113 a0001c0001t0001g0166 a0001c0001t0001g0189 others(1): Show |
4 | HG06807.hp1 NA18965.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.918-696_918-695ins others(1): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423779 | |||||||
| chr2:174423780 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(68): Show |
126 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.918-695T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423780 | |||||||
| chr2:174423781 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.918-694T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423781 | |||||||
| chr2:174423824 | C | T | 2 | a0001c0001t0001g0111 a0007c0010t0001g0148 |
2 | HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.918-651C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423824 | |||||||
| chr2:174423848 | T | C | 52 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(49): Show |
70 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(67): Show |
intron_variant | MODIFIER | c.918-627T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423848 | |||||||
| chr2:174423970 | G | T | 75 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(72): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.918-505G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423970 | |||||||
| chr2:174423980 | G | T | 1 | a0001c0001t0016g0188 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.918-495G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174423980 | |||||||
| chr2:174424127 | C | T | 32 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(29): Show |
41 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(38): Show |
intron_variant | MODIFIER | c.918-348C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174424127 | |||||||
| chr2:174424161 | G | T | 1 | a0002c0002t0002g0214 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.918-314G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174424161 | |||||||
| chr2:174424257 | G | T | 1 | a0002c0002t0002g0225 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.918-218G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174424257 | |||||||
| chr2:174424416 | C | A | 50 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0011 others(47): Show |
87 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.918-59C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 6/7 | chr2 | 174424416 | |||||||
| chr2:174424691 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0132 |
3 | HG02280.hp2 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1092+42G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174424691 | |||||||
| chr2:174424704 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1092+55C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174424704 | |||||||
| chr2:174424774 | G | A | 2 | a0005c0007t0010g0109 a0005c0007t0010g0110 |
2 | NA18964.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1092+125G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174424774 | |||||||
| chr2:174424822 | C | T | 1 | a0009c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1092+173C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174424822 | |||||||
| chr2:174424898 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
131 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.1092+249T>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174424898 | |||||||
| chr2:174424963 | G | T | 1 | a0002c0002t0002g0226 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1092+314G>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174424963 | |||||||
| chr2:174425006 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(227): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1092+357G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174425006 | |||||||
| chr2:174425104 | C | T | 1 | a0002c0002t0002g0067 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1092+455C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174425104 | |||||||
| chr2:174425257 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1092+608G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174425257 | |||||||
| chr2:174425279 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1092+630G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174425279 | |||||||
| chr2:174425643 | T | C | 50 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0011 others(47): Show |
87 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1092+994T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174425643 | |||||||
| chr2:174425917 | A | G | 20 | a0003c0003t0001g0004 a0003c0003t0001g0019 a0003c0003t0001g0035 others(17): Show |
29 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1092+1268A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174425917 | |||||||
| chr2:174426038 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1092+1389A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426038 | |||||||
| chr2:174426089 | T | C | 1 | a0009c0008t0002g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1092+1440T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426089 | |||||||
| chr2:174426092 | G | A | 50 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0011 others(47): Show |
87 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1092+1443G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426092 | |||||||
| chr2:174426314 | A | T | 18 | a0002c0002t0002g0011 a0002c0002t0002g0017 a0002c0002t0002g0059 others(15): Show |
28 | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1093-1399A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426314 | |||||||
| chr2:174426420 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1093-1293C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426420 | |||||||
| chr2:174426646 | C | A | 2 | a0002c0002t0004g0062 a0002c0002t0004g0065 |
2 | HG01515.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1093-1067C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426646 | |||||||
| chr2:174426735 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
131 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.1093-978G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426735 | |||||||
| chr2:174426771 | C | CCAAAA | 31 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(28): Show |
40 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(37): Show |
intron_variant | MODIFIER | c.1093-921_1093-917d others(7): Show |
SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 174426771 | ||||||
| chr2:174426815 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-898C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426815 | |||||||
| chr2:174426816 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-897A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426816 | |||||||
| chr2:174426817 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-896C>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426817 | |||||||
| chr2:174426823 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-890A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426823 | |||||||
| chr2:174426832 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-881T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426832 | |||||||
| chr2:174426837 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-876T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426837 | |||||||
| chr2:174426838 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-875A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426838 | |||||||
| chr2:174426842 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-871A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426842 | |||||||
| chr2:174426846 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-867A>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426846 | |||||||
| chr2:174426850 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-863T>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426850 | |||||||
| chr2:174426856 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-857A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426856 | |||||||
| chr2:174426882 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-831G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426882 | |||||||
| chr2:174426896 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-817G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426896 | |||||||
| chr2:174426897 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1093-816A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426897 | |||||||
| chr2:174426919 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1093-794G>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174426919 | |||||||
| chr2:174427021 | C | T | 50 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0011 others(47): Show |
87 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1093-692C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427021 | |||||||
| chr2:174427076 | C | T | 20 | a0003c0003t0001g0004 a0003c0003t0001g0019 a0003c0003t0001g0035 others(17): Show |
29 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1093-637C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427076 | |||||||
| chr2:174427109 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0112 a0001c0001t0001g0147 others(2): Show |
6 | HG01884.hp2 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1093-604C>T | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427109 | |||||||
| chr2:174427155 | T | C | 50 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0011 others(47): Show |
87 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1093-558T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427155 | |||||||
| chr2:174427318 | A | G | 1 | a0001c0001t0001g0047 | 2 | HG00733.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1093-395A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427318 | |||||||
| chr2:174427506 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1093-207A>G | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427506 | |||||||
| chr2:174427598 | C | A | 104 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(101): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1093-115C>A | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427598 | |||||||
| chr2:174427636 | T | C | 50 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0011 others(47): Show |
87 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.1093-77T>C | SCRN3 | ENSG00000144306.15 | transcript | ENST00000272732.11 | protein_coding | 7/7 | chr2 | 174427636 |