Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 201595 |
| ensemblid | ENSG00000163527.10 |
| hgncid | 30611 |
| symbol | STT3B |
| name | STT3 oligosaccharyltransferase complex catalytic subunit B |
| refseq_nuc | NM_178862.3 |
| refseq_prot | NP_849193.1 |
| ensembl_nuc | ENST00000295770.4 |
| ensembl_prot | ENSP00000295770.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 31532925 |
| end | 31637616 |
| strand | + |
| ver | v1.2 |
| region | chr3:31532925-31637616 |
| region5000 | chr3:31527925-31642616 |
| regionname0 | STT3B_chr3_31532925_31637616 |
| regionname5000 | STT3B_chr3_31527925_31642616 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 826 | 339 | 90 | 52 | 163 | 12 | 20 | 136 | STT3B_chr3_31527925_31642616 | STT3B | MAEPS others(821): Show |
chr3 | 31527925 | 31642616 |
| a0002 | 0/0 | 826 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | MAEPS others(821): Show |
chr3 | 31527925 | 31642616 |
| a0003 | 0/0 | 826 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | MAEPS others(821): Show |
chr3 | 31527925 | 31642616 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2478 | 321 | 76 | 51 | 160 | 12 | 20 | STT3B_chr3_31527925_31642616 | STT3B | ATGGC others(2473): Show |
chr3 | 31527925 | 31642616 | ||
| a0001c0002 | 0/0 | 2478 | 6 | 6 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | ATGGC others(2473): Show |
chr3 | 31527925 | 31642616 | ||
| a0001c0003 | 0/0 | 2478 | 4 | 4 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | ATGGC others(2473): Show |
chr3 | 31527925 | 31642616 | ||
| a0001c0004 | 0/0 | 2478 | 3 | 2 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | ATGGC others(2473): Show |
chr3 | 31527925 | 31642616 | ||
| a0001c0006 | 0/0 | 2478 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | ATGGC others(2473): Show |
chr3 | 31527925 | 31642616 | ||
| a0001c0007 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | ATGGC others(2473): Show |
chr3 | 31527925 | 31642616 | ||
| a0001c0009 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | ATGGC others(2473): Show |
chr3 | 31527925 | 31642616 | ||
| a0001c0010 | 0/0 | 2478 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | ATGGC others(2473): Show |
chr3 | 31527925 | 31642616 | ||
| a0002c0005 | 0/0 | 2478 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | ATGGC others(2473): Show |
chr3 | 31527925 | 31642616 | ||
| a0003c0008 | 0/0 | 2478 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | ATGGC others(2473): Show |
chr3 | 31527925 | 31642616 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4107 | 214 | 52 | 42 | 99 | 7 | 13 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0001t0002 | 0/0 | 4107 | 51 | 0 | 0 | 48 | 0 | 3 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0001t0003 | 1/0 | 4107 | 27 | 15 | 3 | 6 | 0 | 2 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0001t0004 | 0/0 | 4107 | 24 | 8 | 6 | 5 | 3 | 2 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0001t0005 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0001t0006 | 0/0 | 4107 | 2 | 0 | 0 | 0 | 2 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0001t0007 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0001t0008 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0002t0001 | 0/0 | 4107 | 6 | 6 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0003t0001 | 0/0 | 4107 | 4 | 4 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0004t0005 | 0/0 | 4107 | 3 | 2 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0006t0001 | 0/0 | 4107 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0007t0001 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0009t0001 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0001c0010t0002 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0002c0005t0004 | 0/0 | 4107 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| a0003c0008t0001 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | GTCCC others(4102): Show |
chr3 | 31527925 | 31642616 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0008 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0006g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0003t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0004t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0004t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0004t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0006t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0006t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0007t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0009t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0001c0010t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0002c0005t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0002c0005t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| a0003c0008t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | GBR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0175 | EUR | GBR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0182 | EUR | FIN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00423 | hp2 | a0002 | c0005 | t0004 | g0092 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00597 | hp2 | a0001 | c0001 | t0007 | g0160 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00621 | hp1 | a0002 | c0005 | t0004 | g0093 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0179 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0174 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0176 | EUR | IBS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0139 | EUR | IBS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0116 | EUR | IBS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0215 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0224 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01934 | hp1 | a0001 | c0004 | t0005 | g0066 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0173 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02071 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02074 | hp2 | a0001 | c0010 | t0002 | g0044 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02080 | hp2 | a0003 | c0008 | t0001 | g0281 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | CDX | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0192 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0297 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0223 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0191 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03139 | hp2 | a0001 | c0004 | t0005 | g0017 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0221 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03209 | hp2 | a0001 | c0009 | t0001 | g0171 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0218 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0188 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0181 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | STU | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | BEB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0183 | SAS | STU | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0172 | SAS | STU | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | STU | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | YRI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CHB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | YRI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19009 | hp1 | a0001 | c0006 | t0001 | g0090 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0324 | AFR | LWK | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | LWK | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | LWK | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19072 | hp1 | a0001 | c0006 | t0001 | g0117 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19078 | hp2 | a0001 | c0001 | t0008 | g0260 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0208 | AFR | YRI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | ASW | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | GIH | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | GIH | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0178 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0219 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0222 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03471 | hp1 | a0001 | c0007 | t0001 | g0298 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | USA | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | USA | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | USA | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | USA | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| NA21309 | hp2 | a0001 | c0004 | t0005 | g0318 | AFR | LWK | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0167 | REF | REF | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0190 | REF | REF | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:31533134 | G | A | 1 | a0002 | 2 | HG00423.hp2 HG00621.hp1 |
missense_variant | MODERATE | c.136G>A | p.Gly46Ser | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/16 | 210/4107 | 136/2481 | 46/826 | chr3 | 31533134 | |||
| chr3:31622111 | A | G | 1 | a0003 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.1342A>G | p.Ile448Val | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/16 | 1416/4107 | 1342/2481 | 448/826 | chr3 | 31622111 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:31533031 | C | T | 1 | a0001c0010 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.33C>T | p.His11His | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/16 | 107/4107 | 33/2481 | 11/826 | chr3 | 31533031 | |||
| chr3:31533139 | C | T | 1 | a0001c0009 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.141C>T | p.Gly47Gly | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/16 | 215/4107 | 141/2481 | 47/826 | chr3 | 31533139 | |||
| chr3:31533166 | G | A | 1 | a0001c0006 | 2 | NA19009.hp1 NA19072.hp1 |
synonymous_variant | LOW | c.168G>A | p.Ala56Ala | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/16 | 242/4107 | 168/2481 | 56/826 | chr3 | 31533166 | |||
| chr3:31579862 | A | G | 1 | a0001c0002 | 6 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.477A>G | p.Thr159Thr | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/16 | 551/4107 | 477/2481 | 159/826 | chr3 | 31579862 | |||
| chr3:31624950 | C | T | 1 | a0001c0004 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.1764C>T | p.Tyr588Tyr | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 12/16 | 1838/4107 | 1764/2481 | 588/826 | chr3 | 31624950 | |||
| chr3:31633069 | A | G | 1 | a0001c0007 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2322A>G | p.Ala774Ala | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/16 | 2396/4107 | 2322/2481 | 774/826 | chr3 | 31633069 | |||
| chr3:31635989 | C | A | 1 | a0001c0003 | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.2406C>A | p.Thr802Thr | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 2480/4107 | 2406/2481 | 802/826 | chr3 | 31635989 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:31636250 | G | A | 1 | a0001c0001t0006 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*186G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 186 | chr3 | 31636250 | ||||||
| chr3:31636928 | A | G | 2 | a0001c0001t0002 a0001c0010t0002 |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*864A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 864 | chr3 | 31636928 | ||||||
| chr3:31636949 | T | G | 2 | a0001c0001t0005 a0001c0004t0005 |
4 | HG01934.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*885T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 885 | chr3 | 31636949 | ||||||
| chr3:31637020 | A | G | 2 | a0001c0001t0004 a0002c0005t0004 |
26 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*956A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 956 | chr3 | 31637020 | ||||||
| chr3:31637121 | G | A | 16 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(13): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*1057G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 1057 | chr3 | 31637121 | ||||||
| chr3:31637353 | T | C | 1 | a0001c0001t0007 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1289T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 1289 | chr3 | 31637353 | ||||||
| chr3:31637563 | T | G | 1 | a0001c0001t0008 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1499T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 1499 | chr3 | 31637563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:31533337 | C | T | 1 | a0001c0003t0001g0324 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.314+25C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533337 | |||||||
| chr3:31533419 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.314+107C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533419 | |||||||
| chr3:31533423 | C | T | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+111C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533423 | |||||||
| chr3:31533564 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(113): Show |
122 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.314+252A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533564 | |||||||
| chr3:31533652 | G | C | 1 | a0001c0001t0001g0214 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.314+340G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533652 | |||||||
| chr3:31533670 | A | G | 18 | a0001c0001t0001g0197 a0001c0001t0003g0012 a0001c0001t0003g0198 others(15): Show |
19 | HG00735.hp2 HG01123.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.314+358A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533670 | |||||||
| chr3:31533680 | G | C | 206 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(203): Show |
216 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(213): Show |
intron_variant | MODIFIER | c.314+368G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533680 | |||||||
| chr3:31533700 | G | T | 1 | a0001c0001t0004g0196 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.314+388G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533700 | |||||||
| chr3:31533718 | C | T | 5 | a0001c0001t0004g0191 a0001c0001t0004g0192 a0001c0001t0004g0193 others(2): Show |
5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+406C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533718 | |||||||
| chr3:31533779 | C | T | 1 | a0001c0004t0005g0318 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.314+467C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533779 | |||||||
| chr3:31533890 | T | C | 8 | a0001c0001t0001g0323 a0001c0001t0005g0218 a0001c0002t0001g0215 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.314+578T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533890 | |||||||
| chr3:31533976 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.314+664A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533976 | |||||||
| chr3:31534231 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.314+919G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534231 | |||||||
| chr3:31534277 | T | G | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.314+965T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534277 | |||||||
| chr3:31534320 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.314+1008C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534320 | |||||||
| chr3:31534466 | C | A | 1 | a0001c0001t0004g0191 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.314+1154C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534466 | |||||||
| chr3:31534680 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
5 | HG00733.hp2 HG02145.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+1368G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534680 | |||||||
| chr3:31534885 | C | G | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.314+1573C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534885 | |||||||
| chr3:31534896 | T | C | 1 | a0001c0006t0001g0090 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.314+1584T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534896 | |||||||
| chr3:31534943 | T | C | 305 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(302): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.314+1631T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534943 | |||||||
| chr3:31535001 | C | A | 1 | a0001c0001t0001g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.314+1689C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535001 | |||||||
| chr3:31535105 | A | C | 1 | a0001c0001t0001g0189 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.314+1793A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535105 | |||||||
| chr3:31535125 | C | CT | 100 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(97): Show |
106 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.314+1814dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31535125 | ||||||
| chr3:31535335 | TA | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.314+2024delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535335 | |||||||
| chr3:31535339 | T | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(98): Show |
107 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.314+2027T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535339 | |||||||
| chr3:31535340 | T | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.314+2028T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535340 | |||||||
| chr3:31535459 | C | T | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.314+2147C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535459 | |||||||
| chr3:31535463 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.314+2151C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535463 | |||||||
| chr3:31535551 | C | T | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.314+2239C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535551 | |||||||
| chr3:31535962 | C | G | 1 | a0001c0002t0001g0221 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.314+2650C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535962 | |||||||
| chr3:31536035 | A | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+2723A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536035 | |||||||
| chr3:31536051 | C | CA | 5 | a0001c0001t0004g0005 a0001c0001t0004g0094 a0001c0001t0004g0095 others(2): Show |
6 | HG00423.hp2 HG00621.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+2747dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31536051 | ||||||
| chr3:31536052 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.314+2740A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536052 | |||||||
| chr3:31536054 | A | C | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.314+2742A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536054 | |||||||
| chr3:31536081 | T | C | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
95 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.314+2769T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536081 | |||||||
| chr3:31536163 | A | C | 1 | a0001c0001t0001g0170 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.314+2851A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536163 | |||||||
| chr3:31536448 | A | G | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG01069.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.314+3136A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536448 | |||||||
| chr3:31536531 | A | G | 5 | a0001c0001t0004g0191 a0001c0001t0004g0192 a0001c0001t0004g0193 others(2): Show |
5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+3219A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536531 | |||||||
| chr3:31536681 | A | G | 20 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.314+3369A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536681 | |||||||
| chr3:31537096 | C | T | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.314+3784C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31537096 | |||||||
| chr3:31537100 | C | T | 190 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.314+3788C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31537100 | |||||||
| chr3:31537449 | G | GTTACTGA | 29 | a0001c0001t0001g0096 a0001c0001t0003g0187 a0001c0001t0003g0188 others(26): Show |
30 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.314+4140_314+4146d others(9): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31537449 | ||||||
| chr3:31537514 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.314+4202G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31537514 | |||||||
| chr3:31537586 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.314+4274C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31537586 | |||||||
| chr3:31537757 | C | A | 1 | a0002c0005t0004g0092 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.314+4445C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31537757 | |||||||
| chr3:31537770 | A | G | 1 | a0001c0001t0002g0065 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.314+4458A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31537770 | |||||||
| chr3:31538129 | A | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+4817A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538129 | |||||||
| chr3:31538129 | A | T | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.314+4817A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538129 | |||||||
| chr3:31538262 | A | G | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.314+4950A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538262 | |||||||
| chr3:31538479 | A | G | 2 | a0001c0002t0001g0219 a0001c0002t0001g0220 |
2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.314+5167A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538479 | |||||||
| chr3:31538488 | A | AC | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.314+5176_314+5177i others(3): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538488 | |||||||
| chr3:31538607 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.314+5295A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538607 | |||||||
| chr3:31538639 | A | G | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+5327A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538639 | |||||||
| chr3:31538657 | C | T | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+5345C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538657 | |||||||
| chr3:31538963 | A | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+5651A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538963 | |||||||
| chr3:31539004 | G | T | 11 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(8): Show |
11 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.314+5692G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539004 | |||||||
| chr3:31539211 | T | C | 1 | a0001c0001t0002g0018 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.314+5899T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539211 | |||||||
| chr3:31539503 | C | T | 23 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(20): Show |
23 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.314+6191C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539503 | |||||||
| chr3:31539801 | T | C | 24 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(21): Show |
24 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.314+6489T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539801 | |||||||
| chr3:31539881 | G | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
95 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.314+6569G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539881 | |||||||
| chr3:31539915 | A | G | 1 | a0001c0001t0001g0302 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.314+6603A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539915 | |||||||
| chr3:31539920 | C | G | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.314+6608C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539920 | |||||||
| chr3:31540024 | C | A | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | HG01069.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.314+6712C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540024 | |||||||
| chr3:31540277 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.314+6965A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540277 | |||||||
| chr3:31540335 | C | T | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+7023C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540335 | |||||||
| chr3:31540348 | AG | A | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+7039delG | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31540348 | ||||||
| chr3:31540392 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+7080T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540392 | |||||||
| chr3:31540457 | G | A | 18 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(15): Show |
18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.314+7145G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540457 | |||||||
| chr3:31540648 | C | A | 1 | a0001c0002t0001g0217 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.314+7336C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540648 | |||||||
| chr3:31540649 | G | A | 2 | a0001c0004t0005g0017 a0001c0004t0005g0066 |
2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.314+7337G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540649 | |||||||
| chr3:31540716 | A | T | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+7404A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540716 | |||||||
| chr3:31540746 | T | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.314+7434T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540746 | |||||||
| chr3:31540965 | C | T | 1 | a0001c0001t0004g0185 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.314+7653C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540965 | |||||||
| chr3:31541034 | T | A | 1 | a0001c0001t0001g0097 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.314+7722T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541034 | |||||||
| chr3:31541063 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.314+7751C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541063 | |||||||
| chr3:31541066 | G | A | 8 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
8 | HG01070.hp1 HG01358.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.314+7754G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541066 | |||||||
| chr3:31541213 | A | C | 24 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(21): Show |
24 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.314+7901A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541213 | |||||||
| chr3:31541226 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.314+7914T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541226 | |||||||
| chr3:31541356 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | NA19007.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.314+8044T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541356 | |||||||
| chr3:31541380 | G | A | 1 | a0001c0001t0003g0198 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.314+8068G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541380 | |||||||
| chr3:31541472 | G | GT | 19 | a0001c0001t0001g0016 a0001c0001t0001g0161 a0001c0001t0001g0162 others(16): Show |
20 | HG00438.hp2 HG00639.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.314+8175dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31541472 | ||||||
| chr3:31541478 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.314+8166T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541478 | |||||||
| chr3:31541528 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 |
3 | HG01243.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.314+8216G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541528 | |||||||
| chr3:31541620 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.314+8308G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541620 | |||||||
| chr3:31541871 | C | G | 1 | a0001c0007t0001g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.314+8559C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541871 | |||||||
| chr3:31541911 | C | T | 1 | a0001c0001t0003g0297 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.314+8599C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541911 | |||||||
| chr3:31541932 | C | G | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.314+8620C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541932 | |||||||
| chr3:31542040 | C | T | 1 | a0001c0001t0007g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.314+8728C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542040 | |||||||
| chr3:31542140 | G | A | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.314+8828G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542140 | |||||||
| chr3:31542168 | C | T | 1 | a0001c0001t0004g0184 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.314+8856C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542168 | |||||||
| chr3:31542344 | C | G | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.314+9032C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542344 | |||||||
| chr3:31542402 | G | A | 6 | a0001c0001t0003g0236 a0001c0001t0003g0237 a0001c0001t0003g0238 others(3): Show |
6 | HG01167.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+9090G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542402 | |||||||
| chr3:31542598 | T | G | 1 | a0001c0001t0003g0297 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.314+9286T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542598 | |||||||
| chr3:31542761 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.314+9449T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542761 | |||||||
| chr3:31542775 | A | G | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+9463A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542775 | |||||||
| chr3:31542791 | C | G | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.314+9479C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542791 | |||||||
| chr3:31542856 | C | G | 1 | a0001c0001t0003g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.314+9544C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542856 | |||||||
| chr3:31542946 | A | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.314+9634A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542946 | |||||||
| chr3:31542958 | C | G | 2 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
2 | NA18993.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.314+9646C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542958 | |||||||
| chr3:31542959 | G | C | 1 | a0001c0001t0001g0241 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.314+9647G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542959 | |||||||
| chr3:31542964 | G | A | 2 | a0001c0004t0005g0017 a0001c0004t0005g0318 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+9652G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542964 | |||||||
| chr3:31543061 | A | G | 25 | a0001c0001t0004g0005 a0001c0001t0004g0094 a0001c0001t0004g0095 others(22): Show |
26 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.314+9749A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31543061 | |||||||
| chr3:31543067 | C | CA | 67 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(64): Show |
72 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.314+9772dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31543067 | ||||||
| chr3:31543067 | C | CAAAA | 80 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(77): Show |
87 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.314+9769_314+9772d others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31543067 | ||||||
| chr3:31543067 | C | CAAAAA | 70 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0067 others(67): Show |
73 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.314+9768_314+9772d others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31543067 | ||||||
| chr3:31543067 | C | CAAAAAA | 33 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0073 others(30): Show |
34 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.314+9767_314+9772d others(8): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31543067 | ||||||
| chr3:31543067 | C | CAAAAAAA | 6 | a0001c0001t0001g0072 a0001c0001t0004g0191 a0001c0001t0004g0192 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+9766_314+9772d others(9): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31543067 | ||||||
| chr3:31543328 | A | G | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.314+10016A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31543328 | |||||||
| chr3:31543449 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.314+10137A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31543449 | |||||||
| chr3:31543468 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.314+10156G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31543468 | |||||||
| chr3:31543803 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.314+10491G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31543803 | |||||||
| chr3:31544038 | T | C | 1 | a0002c0005t0004g0092 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.314+10726T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31544038 | |||||||
| chr3:31544154 | A | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+10842A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31544154 | |||||||
| chr3:31544544 | G | A | 5 | a0001c0001t0001g0283 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+11232G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31544544 | |||||||
| chr3:31544711 | C | G | 5 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(2): Show |
5 | HG01975.hp2 HG02080.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+11399C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31544711 | |||||||
| chr3:31544737 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+11425C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31544737 | |||||||
| chr3:31544944 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.314+11632G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31544944 | |||||||
| chr3:31545076 | G | A | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.314+11764G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545076 | |||||||
| chr3:31545171 | G | T | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.314+11859G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545171 | |||||||
| chr3:31545396 | G | A | 187 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(184): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.314+12084G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545396 | |||||||
| chr3:31545631 | TTAGTTTC others(17): Show |
T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.314+12320_314+1234 others(28): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545631 | |||||||
| chr3:31545676 | T | G | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+12364T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545676 | |||||||
| chr3:31545759 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.314+12447G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545759 | |||||||
| chr3:31545814 | G | GT | 12 | a0001c0001t0001g0070 a0001c0001t0001g0154 a0001c0001t0001g0155 others(9): Show |
12 | HG00438.hp2 HG02027.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.314+12520dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31545814 | ||||||
| chr3:31545814 | G | T | 13 | a0001c0001t0001g0067 a0001c0001t0001g0076 a0001c0001t0001g0077 others(10): Show |
13 | HG01192.hp2 HG01255.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.314+12502G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545814 | |||||||
| chr3:31545814 | GT | G | 159 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(156): Show |
168 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.314+12520delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31545814 | ||||||
| chr3:31545814 | GTT | G | 11 | a0001c0001t0001g0016 a0001c0001t0001g0278 a0001c0001t0001g0308 others(8): Show |
12 | HG00639.hp1 HG01884.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.314+12519_314+1252 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31545814 | ||||||
| chr3:31545848 | C | G | 1 | a0001c0002t0001g0216 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314+12536C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545848 | |||||||
| chr3:31545919 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0313 a0001c0001t0001g0314 |
4 | HG00639.hp1 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+12607A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545919 | |||||||
| chr3:31546000 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.314+12688C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546000 | |||||||
| chr3:31546274 | G | C | 1 | a0001c0001t0001g0242 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.314+12962G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546274 | |||||||
| chr3:31546293 | TGTA | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(71): Show |
79 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.314+12984_314+1298 others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31546293 | ||||||
| chr3:31546419 | A | G | 1 | a0001c0001t0004g0183 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.314+13107A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546419 | |||||||
| chr3:31546444 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.314+13132A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546444 | |||||||
| chr3:31546479 | G | C | 1 | a0001c0001t0002g0027 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.314+13167G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546479 | |||||||
| chr3:31546799 | T | C | 2 | a0001c0004t0005g0017 a0001c0004t0005g0318 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+13487T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546799 | |||||||
| chr3:31546828 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.314+13516T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546828 | |||||||
| chr3:31546845 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.314+13533G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546845 | |||||||
| chr3:31546916 | C | G | 1 | a0001c0001t0001g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.314+13604C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546916 | |||||||
| chr3:31546925 | G | A | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.314+13613G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546925 | |||||||
| chr3:31546988 | G | T | 1 | a0001c0001t0001g0153 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.314+13676G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546988 | |||||||
| chr3:31547059 | T | G | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+13747T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547059 | |||||||
| chr3:31547199 | C | T | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.314+13887C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547199 | |||||||
| chr3:31547385 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.314+14073C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547385 | |||||||
| chr3:31547460 | T | A | 8 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0296 others(5): Show |
8 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.314+14148T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547460 | |||||||
| chr3:31547503 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.314+14191G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547503 | |||||||
| chr3:31547520 | C | T | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.314+14208C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547520 | |||||||
| chr3:31547790 | T | A | 10 | a0001c0001t0004g0172 a0001c0001t0004g0173 a0001c0001t0004g0174 others(7): Show |
10 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.314+14478T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547790 | |||||||
| chr3:31547853 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.314+14541T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547853 | |||||||
| chr3:31548105 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.314+14793A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548105 | |||||||
| chr3:31548176 | G | A | 5 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(2): Show |
5 | HG03225.hp1 NA18951.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.314+14864G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548176 | |||||||
| chr3:31548209 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.314+14897A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548209 | |||||||
| chr3:31548335 | GA | G | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.314+15031delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31548335 | ||||||
| chr3:31548573 | T | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.314+15261T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548573 | |||||||
| chr3:31548730 | A | C | 4 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(1): Show |
4 | HG02027.hp2 NA18945.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+15418A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548730 | |||||||
| chr3:31548797 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): Show |
78 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.314+15485G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548797 | |||||||
| chr3:31548878 | C | G | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
95 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.314+15566C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548878 | |||||||
| chr3:31548934 | T | C | 1 | a0001c0001t0002g0028 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.314+15622T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548934 | |||||||
| chr3:31549310 | CT | C | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.314+15999delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549310 | |||||||
| chr3:31549412 | T | G | 1 | a0001c0001t0001g0110 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.314+16100T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549412 | |||||||
| chr3:31549530 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.314+16218A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549530 | |||||||
| chr3:31549586 | T | C | 1 | a0001c0001t0002g0028 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.314+16274T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549586 | |||||||
| chr3:31549741 | A | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0058 a0001c0001t0001g0059 others(9): Show |
14 | HG02027.hp2 NA18944.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.314+16429A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549741 | |||||||
| chr3:31549742 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.314+16430T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549742 | |||||||
| chr3:31549767 | A | G | 11 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(8): Show |
11 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.314+16455A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549767 | |||||||
| chr3:31549799 | G | A | 1 | a0001c0001t0004g0172 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.314+16487G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549799 | |||||||
| chr3:31549848 | A | C | 1 | a0001c0001t0001g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.314+16536A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549848 | |||||||
| chr3:31549894 | T | C | 2 | a0001c0004t0005g0017 a0001c0004t0005g0318 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+16582T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549894 | |||||||
| chr3:31550071 | ATTAGT | A | 9 | a0001c0001t0002g0022 a0001c0001t0002g0029 a0001c0001t0002g0030 others(6): Show |
9 | NA18942.hp2 NA18944.hp2 NA18993.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+16765_314+1676 others(9): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31550071 | ||||||
| chr3:31550308 | A | C | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+16996A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550308 | |||||||
| chr3:31550308 | A | T | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+16996A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550308 | |||||||
| chr3:31550513 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.314+17201G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550513 | |||||||
| chr3:31550656 | G | A | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+17344G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550656 | |||||||
| chr3:31550692 | T | G | 1 | a0001c0001t0001g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.314+17380T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550692 | |||||||
| chr3:31550765 | T | C | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+17453T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550765 | |||||||
| chr3:31550769 | G | A | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+17457G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550769 | |||||||
| chr3:31550773 | G | GT | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+17468dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31550773 | ||||||
| chr3:31550778 | T | C | 13 | a0001c0001t0001g0002 a0001c0001t0001g0227 a0001c0001t0001g0241 others(10): Show |
15 | HG00558.hp1 HG02027.hp2 NA18945.hp1 others(12): Show |
intron_variant | MODIFIER | c.314+17466T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550778 | |||||||
| chr3:31550978 | G | A | 20 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.314+17666G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550978 | |||||||
| chr3:31551201 | T | TTTTG | 107 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(104): Show |
114 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.314+17914_314+1791 others(8): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31551201 | ||||||
| chr3:31551201 | T | TTTTGTTT others(1): Show |
6 | a0001c0001t0001g0270 a0001c0001t0001g0312 a0001c0001t0001g0319 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+17910_314+1791 others(12): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31551201 | ||||||
| chr3:31551226 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.314+17914T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551226 | |||||||
| chr3:31551255 | A | G | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.314+17943A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551255 | |||||||
| chr3:31551261 | A | G | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.314+17949A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551261 | |||||||
| chr3:31551323 | C | G | 2 | a0001c0001t0003g0012 a0001c0001t0003g0212 |
3 | NA18948.hp2 NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.314+18011C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551323 | |||||||
| chr3:31551357 | A | G | 2 | a0001c0004t0005g0017 a0001c0004t0005g0066 |
2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.314+18045A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551357 | |||||||
| chr3:31551419 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.314+18107G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551419 | |||||||
| chr3:31551692 | G | C | 1 | a0001c0001t0001g0241 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.314+18380G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551692 | |||||||
| chr3:31551781 | T | C | 1 | a0001c0001t0001g0247 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.314+18469T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551781 | |||||||
| chr3:31551840 | T | C | 1 | a0001c0001t0003g0199 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.314+18528T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551840 | |||||||
| chr3:31551882 | G | GCTTCTAA | 6 | a0001c0002t0001g0215 a0001c0002t0001g0216 a0001c0002t0001g0217 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+18571_314+1857 others(11): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31551882 | ||||||
| chr3:31551884 | A | T | 6 | a0001c0002t0001g0215 a0001c0002t0001g0216 a0001c0002t0001g0217 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+18572A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551884 | |||||||
| chr3:31551886 | G | C | 6 | a0001c0002t0001g0215 a0001c0002t0001g0216 a0001c0002t0001g0217 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+18574G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551886 | |||||||
| chr3:31551887 | G | T | 6 | a0001c0002t0001g0215 a0001c0002t0001g0216 a0001c0002t0001g0217 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+18575G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551887 | |||||||
| chr3:31551967 | G | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.314+18655G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551967 | |||||||
| chr3:31551978 | T | TA | 5 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0033 others(2): Show |
7 | NA18950.hp2 NA18962.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+18667dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31551978 | ||||||
| chr3:31552150 | G | T | 1 | a0001c0001t0001g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.314+18838G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552150 | |||||||
| chr3:31552328 | G | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.314+19016G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552328 | |||||||
| chr3:31552396 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | NA18962.hp1 NA18990.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.314+19084A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552396 | |||||||
| chr3:31552494 | T | C | 9 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(6): Show |
9 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.314+19182T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552494 | |||||||
| chr3:31552517 | CT | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+19214delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31552517 | ||||||
| chr3:31552595 | A | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+19283A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552595 | |||||||
| chr3:31552617 | G | A | 1 | a0001c0001t0003g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.314+19305G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552617 | |||||||
| chr3:31552712 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.314+19400C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552712 | |||||||
| chr3:31552777 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.314+19465T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552777 | |||||||
| chr3:31552795 | A | G | 18 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(15): Show |
18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.314+19483A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552795 | |||||||
| chr3:31552823 | G | T | 3 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 |
3 | HG00735.hp2 HG01123.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.314+19511G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552823 | |||||||
| chr3:31552958 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.314+19646C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552958 | |||||||
| chr3:31553097 | G | A | 2 | a0001c0001t0005g0218 a0001c0004t0005g0017 |
2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.314+19785G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553097 | |||||||
| chr3:31553101 | C | CA | 92 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0067 others(89): Show |
95 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314+19807dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31553101 | ||||||
| chr3:31553101 | C | CAA | 10 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0075 others(7): Show |
10 | HG01192.hp2 HG01243.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.314+19806_314+1980 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31553101 | ||||||
| chr3:31553120 | C | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0320 |
2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.314+19808C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553120 | |||||||
| chr3:31553434 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.314+20122T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553434 | |||||||
| chr3:31553450 | G | T | 1 | a0001c0001t0003g0188 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.314+20138G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553450 | |||||||
| chr3:31553476 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.314+20164C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553476 | |||||||
| chr3:31553570 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | NA19007.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.314+20258A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553570 | |||||||
| chr3:31553608 | C | T | 5 | a0001c0001t0004g0191 a0001c0001t0004g0192 a0001c0001t0004g0193 others(2): Show |
5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+20296C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553608 | |||||||
| chr3:31553856 | T | C | 1 | a0001c0001t0001g0323 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.314+20544T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553856 | |||||||
| chr3:31553927 | ATTTGAGA others(8): Show |
A | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.314+20616_314+2063 others(19): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553927 | |||||||
| chr3:31553992 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(90): Show |
99 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.314+20680A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553992 | |||||||
| chr3:31554252 | T | A | 1 | a0002c0005t0004g0093 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.314+20940T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31554252 | |||||||
| chr3:31554529 | T | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | NA18980.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.314+21217T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31554529 | |||||||
| chr3:31554540 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.314+21228C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31554540 | |||||||
| chr3:31554707 | T | C | 1 | a0001c0001t0002g0030 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.314+21395T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31554707 | |||||||
| chr3:31554714 | T | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.314+21402T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31554714 | |||||||
| chr3:31554884 | C | A | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-21512C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31554884 | |||||||
| chr3:31555119 | C | T | 182 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.315-21277C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555119 | |||||||
| chr3:31555162 | T | C | 1 | a0001c0001t0002g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.315-21234T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555162 | |||||||
| chr3:31555173 | T | G | 1 | a0001c0001t0004g0173 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.315-21223T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555173 | |||||||
| chr3:31555274 | T | C | 1 | a0001c0001t0002g0186 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.315-21122T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555274 | |||||||
| chr3:31555459 | A | C | 1 | a0001c0001t0004g0179 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.315-20937A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555459 | |||||||
| chr3:31555475 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0087 a0001c0001t0001g0088 others(2): Show |
6 | HG00733.hp2 HG00741.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-20921G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555475 | |||||||
| chr3:31555483 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.315-20913C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555483 | |||||||
| chr3:31555680 | G | T | 1 | a0001c0001t0001g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.315-20716G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555680 | |||||||
| chr3:31555716 | C | T | 182 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.315-20680C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555716 | |||||||
| chr3:31555837 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0161 |
2 | HG01168.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.315-20559T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555837 | |||||||
| chr3:31555848 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.315-20548A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555848 | |||||||
| chr3:31555942 | A | G | 25 | a0001c0001t0004g0005 a0001c0001t0004g0094 a0001c0001t0004g0095 others(22): Show |
26 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.315-20454A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555942 | |||||||
| chr3:31555982 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.315-20414A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555982 | |||||||
| chr3:31556101 | T | C | 1 | a0001c0001t0002g0036 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.315-20295T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31556101 | |||||||
| chr3:31556110 | C | CT | 6 | a0001c0001t0001g0111 a0001c0001t0001g0144 a0001c0001t0001g0293 others(3): Show |
6 | HG01884.hp2 HG02300.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-20273dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31556110 | ||||||
| chr3:31556446 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-19950G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31556446 | |||||||
| chr3:31556470 | A | G | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.315-19926A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31556470 | |||||||
| chr3:31556698 | T | C | 2 | a0001c0001t0004g0180 a0001c0001t0004g0181 |
2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.315-19698T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31556698 | |||||||
| chr3:31556705 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.315-19691A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31556705 | |||||||
| chr3:31556797 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-19599T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31556797 | |||||||
| chr3:31557224 | G | T | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-19172G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557224 | |||||||
| chr3:31557560 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.315-18836G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557560 | |||||||
| chr3:31557611 | G | GTA | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-18777_315-1877 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31557611 | ||||||
| chr3:31557724 | C | T | 1 | a0001c0004t0005g0318 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.315-18672C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557724 | |||||||
| chr3:31557757 | C | T | 7 | a0001c0001t0001g0242 a0001c0001t0001g0266 a0001c0001t0001g0267 others(4): Show |
7 | NA18951.hp2 NA18964.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-18639C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557757 | |||||||
| chr3:31557781 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.315-18615C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557781 | |||||||
| chr3:31557784 | C | T | 109 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.315-18612C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557784 | |||||||
| chr3:31557806 | A | G | 186 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.315-18590A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557806 | |||||||
| chr3:31557850 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.315-18546T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557850 | |||||||
| chr3:31557909 | C | T | 10 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0076 others(7): Show |
10 | HG01192.hp2 HG01255.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.315-18487C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557909 | |||||||
| chr3:31558029 | C | T | 1 | a0001c0001t0003g0208 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.315-18367C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31558029 | |||||||
| chr3:31558078 | G | A | 2 | a0001c0004t0005g0017 a0001c0004t0005g0066 |
2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.315-18318G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31558078 | |||||||
| chr3:31558154 | A | G | 1 | a0001c0001t0002g0053 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.315-18242A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31558154 | |||||||
| chr3:31558287 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.315-18109T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31558287 | |||||||
| chr3:31558540 | C | T | 50 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(47): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.315-17856C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31558540 | |||||||
| chr3:31558702 | T | A | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.315-17694T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31558702 | |||||||
| chr3:31558863 | GT | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(183): Show |
196 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.315-17519delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31558863 | ||||||
| chr3:31559021 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.315-17375A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559021 | |||||||
| chr3:31559045 | C | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0264 |
3 | NA18950.hp1 NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.315-17351C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559045 | |||||||
| chr3:31559143 | T | TGG | 10 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0249 others(7): Show |
10 | HG01069.hp2 HG01070.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.315-17250_315-1724 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559143 | ||||||
| chr3:31559146 | G | GGT | 7 | a0001c0001t0001g0099 a0001c0001t0001g0268 a0001c0001t0003g0203 others(4): Show |
7 | HG02258.hp2 HG06807.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-17207_315-1720 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | ||||||
| chr3:31559146 | GGT | G | 65 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(62): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.315-17207_315-1720 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | ||||||
| chr3:31559146 | GGTGT | G | 35 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0088 others(32): Show |
36 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.315-17209_315-1720 others(8): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | ||||||
| chr3:31559146 | GGTGTGT | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0078 a0001c0001t0001g0079 others(29): Show |
33 | HG00735.hp2 HG01069.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.315-17211_315-1720 others(10): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | ||||||
| chr3:31559146 | GGTGTGTG others(1): Show |
G | 32 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0072 others(29): Show |
34 | HG00280.hp2 HG00423.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.315-17213_315-1720 others(12): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | ||||||
| chr3:31559146 | GGTGTGTG others(3): Show |
G | 4 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0085 others(1): Show |
4 | HG02257.hp1 HG02615.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-17215_315-1720 others(14): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | ||||||
| chr3:31559146 | GGTGTGTG others(5): Show |
G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
6 | HG00735.hp1 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-17217_315-1720 others(16): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | ||||||
| chr3:31559146 | GGTGTGTG others(11): Show |
G | 1 | a0001c0009t0001g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.315-17223_315-1720 others(22): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | ||||||
| chr3:31559148 | T | G | 43 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(40): Show |
48 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.315-17248T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559148 | |||||||
| chr3:31559150 | T | G | 4 | a0001c0001t0001g0232 a0001c0001t0001g0251 a0001c0001t0001g0270 others(1): Show |
4 | HG00738.hp1 HG01358.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-17246T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559150 | |||||||
| chr3:31559152 | T | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0108 a0001c0001t0001g0150 others(7): Show |
11 | HG00639.hp2 HG01070.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.315-17244T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559152 | |||||||
| chr3:31559154 | T | G | 9 | a0001c0001t0001g0244 a0001c0001t0004g0192 a0001c0001t0004g0195 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-17242T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559154 | |||||||
| chr3:31559179 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0002g0029 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.315-17216_315-1720 others(16): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559179 | |||||||
| chr3:31559181 | GTGTGTGT others(3): Show |
G | 45 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(42): Show |
48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.315-17214_315-1720 others(14): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559181 | |||||||
| chr3:31559183 | GTGTGTGT others(1): Show |
G | 4 | a0001c0001t0002g0026 a0001c0001t0002g0039 a0001c0001t0002g0049 others(1): Show |
4 | NA19054.hp2 NA19080.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-17212_315-1720 others(12): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559183 | |||||||
| chr3:31559191 | T | G | 1 | a0001c0001t0002g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.315-17205T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559191 | |||||||
| chr3:31559349 | A | ACTTATCT | 217 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(214): Show |
228 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.315-17043_315-1704 others(11): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559349 | ||||||
| chr3:31559443 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG00673.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.315-16953A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559443 | |||||||
| chr3:31559516 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0189 |
2 | HG02027.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.315-16880T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559516 | |||||||
| chr3:31559609 | G | T | 109 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.315-16787G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559609 | |||||||
| chr3:31559772 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.315-16624G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559772 | |||||||
| chr3:31560001 | C | T | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.315-16395C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560001 | |||||||
| chr3:31560007 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.315-16389C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560007 | |||||||
| chr3:31560086 | A | G | 1 | a0001c0001t0004g0191 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.315-16310A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560086 | |||||||
| chr3:31560121 | T | C | 11 | a0001c0001t0004g0172 a0001c0001t0004g0173 a0001c0001t0004g0174 others(8): Show |
11 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.315-16275T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560121 | |||||||
| chr3:31560331 | G | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.315-16065G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560331 | |||||||
| chr3:31560557 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.315-15839A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560557 | |||||||
| chr3:31560590 | G | T | 1 | a0001c0001t0004g0005 | 2 | NA18964.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.315-15806G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560590 | |||||||
| chr3:31560618 | T | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(73): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.315-15778T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560618 | |||||||
| chr3:31560799 | C | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-15597C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560799 | |||||||
| chr3:31560826 | T | C | 111 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(108): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.315-15570T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560826 | |||||||
| chr3:31560931 | T | TCATGTTT others(321): Show |
1 | a0001c0001t0003g0212 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.315-15456_315-1545 others(332): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31560931 | ||||||
| chr3:31560972 | G | T | 2 | a0001c0001t0002g0050 a0001c0001t0002g0051 |
2 | NA18946.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.315-15424G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560972 | |||||||
| chr3:31560983 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(79): Show |
88 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.315-15413A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560983 | |||||||
| chr3:31561283 | A | T | 1 | a0001c0001t0001g0078 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.315-15113A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561283 | |||||||
| chr3:31561448 | T | A | 6 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0076 others(3): Show |
6 | HG01192.hp2 HG01255.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-14948T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561448 | |||||||
| chr3:31561463 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.315-14933G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561463 | |||||||
| chr3:31561586 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-14810T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561586 | |||||||
| chr3:31561670 | G | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-14726G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561670 | |||||||
| chr3:31561716 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-14680T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561716 | |||||||
| chr3:31561724 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.315-14672G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561724 | |||||||
| chr3:31561815 | T | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0001g0120 others(4): Show |
8 | HG00544.hp1 NA18965.hp2 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-14581T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561815 | |||||||
| chr3:31561816 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.315-14580G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561816 | |||||||
| chr3:31561855 | T | C | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-14541T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561855 | |||||||
| chr3:31561982 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(73): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.315-14414G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561982 | |||||||
| chr3:31562002 | C | G | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-14394C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562002 | |||||||
| chr3:31562061 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.315-14335C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562061 | |||||||
| chr3:31562099 | A | T | 1 | a0001c0001t0001g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-14297A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562099 | |||||||
| chr3:31562224 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0088 |
2 | HG02145.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.315-14172G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562224 | |||||||
| chr3:31562357 | G | C | 1 | a0001c0001t0004g0094 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.315-14039G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562357 | |||||||
| chr3:31562614 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.315-13782C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562614 | |||||||
| chr3:31562815 | A | G | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.315-13581A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562815 | |||||||
| chr3:31562838 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.315-13558G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562838 | |||||||
| chr3:31563156 | T | C | 1 | a0001c0004t0005g0017 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.315-13240T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31563156 | |||||||
| chr3:31563228 | C | T | 107 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.315-13168C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31563228 | |||||||
| chr3:31563368 | C | G | 1 | a0001c0001t0001g0252 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.315-13028C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31563368 | |||||||
| chr3:31563833 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-12563C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31563833 | |||||||
| chr3:31563886 | A | G | 85 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(82): Show |
91 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.315-12510A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31563886 | |||||||
| chr3:31564002 | T | G | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-12394T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564002 | |||||||
| chr3:31564053 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG01167.hp1 HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.315-12343A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564053 | |||||||
| chr3:31564090 | A | G | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-12306A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564090 | |||||||
| chr3:31564112 | A | G | 1 | a0001c0001t0003g0200 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.315-12284A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564112 | |||||||
| chr3:31564242 | T | C | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.315-12154T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564242 | |||||||
| chr3:31564267 | G | T | 1 | a0001c0001t0002g0051 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.315-12129G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564267 | |||||||
| chr3:31564557 | G | A | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-11839G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564557 | |||||||
| chr3:31564595 | A | G | 192 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.315-11801A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564595 | |||||||
| chr3:31564636 | G | A | 7 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-11760G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564636 | |||||||
| chr3:31564702 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.315-11694G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564702 | |||||||
| chr3:31564984 | T | C | 1 | a0001c0001t0004g0174 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.315-11412T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564984 | |||||||
| chr3:31565073 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.315-11323T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565073 | |||||||
| chr3:31565269 | A | C | 1 | a0001c0001t0001g0320 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.315-11127A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565269 | |||||||
| chr3:31565288 | C | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(278): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.315-11108C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565288 | |||||||
| chr3:31565431 | T | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.315-10965T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565431 | |||||||
| chr3:31565651 | C | T | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-10745C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565651 | |||||||
| chr3:31565846 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-10550C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565846 | |||||||
| chr3:31565864 | T | G | 1 | a0001c0001t0001g0121 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.315-10532T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565864 | |||||||
| chr3:31565926 | A | T | 2 | a0001c0004t0005g0017 a0001c0004t0005g0318 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.315-10470A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565926 | |||||||
| chr3:31566295 | C | T | 15 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(12): Show |
15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.315-10101C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31566295 | |||||||
| chr3:31566420 | G | T | 1 | a0001c0001t0003g0012 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.315-9976G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31566420 | |||||||
| chr3:31566451 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.315-9945G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31566451 | |||||||
| chr3:31566580 | C | T | 2 | a0001c0001t0006g0116 a0001c0001t0006g0139 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.315-9816C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31566580 | |||||||
| chr3:31566684 | A | T | 1 | a0001c0001t0001g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.315-9712A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31566684 | |||||||
| chr3:31566761 | C | T | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-9635C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31566761 | |||||||
| chr3:31567491 | T | C | 4 | a0001c0001t0001g0242 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | NA18964.hp2 NA18965.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-8905T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567491 | |||||||
| chr3:31567527 | C | T | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-8869C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567527 | |||||||
| chr3:31567544 | C | A | 1 | a0001c0001t0003g0236 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.315-8852C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567544 | |||||||
| chr3:31567582 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.315-8814G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567582 | |||||||
| chr3:31567694 | A | G | 1 | a0001c0002t0001g0217 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.315-8702A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567694 | |||||||
| chr3:31567725 | A | G | 50 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(47): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.315-8671A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567725 | |||||||
| chr3:31567781 | G | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | NA18962.hp1 NA18990.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.315-8615G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567781 | |||||||
| chr3:31567825 | G | A | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-8571G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567825 | |||||||
| chr3:31568029 | AATCATCA others(20): Show |
A | 1 | a0001c0001t0001g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.315-8365_315-8339d others(29): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31568029 | ||||||
| chr3:31568112 | G | T | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-8284G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568112 | |||||||
| chr3:31568158 | G | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01358.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.315-8238G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568158 | |||||||
| chr3:31568792 | G | T | 1 | a0001c0001t0001g0275 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.315-7604G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568792 | |||||||
| chr3:31568837 | C | G | 1 | a0001c0001t0001g0311 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.315-7559C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568837 | |||||||
| chr3:31568868 | A | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-7528A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568868 | |||||||
| chr3:31568946 | G | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.315-7450G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568946 | |||||||
| chr3:31568974 | A | G | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0144 others(1): Show |
4 | HG01358.hp2 HG01496.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-7422A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568974 | |||||||
| chr3:31569073 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-7323G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569073 | |||||||
| chr3:31569287 | A | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(296): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.315-7109A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569287 | |||||||
| chr3:31569425 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.315-6971C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569425 | |||||||
| chr3:31569432 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-6964C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569432 | |||||||
| chr3:31569491 | G | A | 1 | a0001c0001t0001g0243 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.315-6905G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569491 | |||||||
| chr3:31569550 | C | A | 1 | a0001c0001t0003g0012 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.315-6846C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569550 | |||||||
| chr3:31569609 | A | G | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.315-6787A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569609 | |||||||
| chr3:31569800 | T | A | 1 | a0001c0001t0001g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-6596T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569800 | |||||||
| chr3:31569826 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.315-6570G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569826 | |||||||
| chr3:31569876 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | NA19007.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.315-6520A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569876 | |||||||
| chr3:31569931 | T | C | 1 | a0002c0005t0004g0093 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.315-6465T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569931 | |||||||
| chr3:31570126 | G | A | 20 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.315-6270G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570126 | |||||||
| chr3:31570286 | A | G | 192 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.315-6110A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570286 | |||||||
| chr3:31570468 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.315-5928C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570468 | |||||||
| chr3:31570524 | G | A | 15 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(12): Show |
15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.315-5872G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570524 | |||||||
| chr3:31570687 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.315-5709T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570687 | |||||||
| chr3:31570743 | T | C | 118 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.315-5653T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570743 | |||||||
| chr3:31570846 | T | C | 9 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(6): Show |
9 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.315-5550T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570846 | |||||||
| chr3:31571029 | A | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-5367A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571029 | |||||||
| chr3:31571283 | A | AT | 187 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(184): Show |
199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.315-5099dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31571283 | ||||||
| chr3:31571283 | A | ATT | 95 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0059 others(92): Show |
100 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.315-5100_315-5099d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31571283 | ||||||
| chr3:31571362 | A | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.315-5034A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571362 | |||||||
| chr3:31571384 | G | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.315-5012G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571384 | |||||||
| chr3:31571610 | A | T | 1 | a0001c0001t0004g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.315-4786A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571610 | |||||||
| chr3:31571647 | A | G | 7 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0001g0319 others(4): Show |
7 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-4749A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571647 | |||||||
| chr3:31571800 | G | T | 50 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(47): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.315-4596G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571800 | |||||||
| chr3:31571934 | T | TATTA | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.315-4461_315-4458d others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31571934 | ||||||
| chr3:31571980 | T | C | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.315-4416T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571980 | |||||||
| chr3:31572015 | C | CATATTAA others(18): Show |
74 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(71): Show |
79 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.315-4368_315-4344d others(27): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572015 | ||||||
| chr3:31572015 | C | CATATTAA others(43): Show |
9 | a0001c0001t0001g0016 a0001c0001t0001g0243 a0001c0001t0001g0308 others(6): Show |
10 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.315-4344_315-4343i others(52): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572015 | ||||||
| chr3:31572015 | CATATTAA others(3): Show |
C | 2 | a0001c0001t0003g0206 a0001c0001t0003g0207 |
2 | HG02040.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.315-4368_315-4359d others(12): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572015 | ||||||
| chr3:31572015 | CATATTAA others(18): Show |
C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
93 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.315-4368_315-4344d others(27): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572015 | ||||||
| chr3:31572023 | TATATATT others(8): Show |
T | 1 | a0001c0004t0005g0318 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.315-4358_315-4344d others(17): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572023 | ||||||
| chr3:31572026 | ATATTAAT others(26): Show |
A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | NA18975.hp2 NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.315-4367_315-4335d others(35): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572026 | ||||||
| chr3:31572035 | T | TG | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-4361_315-4360i others(3): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572035 | |||||||
| chr3:31572037 | T | TATATTAA others(79): Show |
4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-4359_315-4358i others(88): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572037 | |||||||
| chr3:31572038 | G | A | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-4358G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572038 | |||||||
| chr3:31572038 | G | GATATATT others(50): Show |
1 | a0001c0001t0001g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.315-4344_315-4343i others(59): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572038 | ||||||
| chr3:31572038 | G | GATATATT others(82): Show |
4 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0296 others(1): Show |
4 | HG02622.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-4344_315-4343i others(91): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572038 | ||||||
| chr3:31572056 | A | ATATTAAT others(24): Show |
8 | a0001c0001t0001g0323 a0001c0001t0005g0218 a0001c0002t0001g0215 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.315-4333_315-4303d others(33): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572056 | ||||||
| chr3:31572061 | A | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | NA18975.hp2 NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.315-4335A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572061 | |||||||
| chr3:31572066 | A | G | 1 | a0001c0001t0007g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.315-4330A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572066 | |||||||
| chr3:31572094 | G | A | 191 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.315-4302G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572094 | |||||||
| chr3:31572094 | G | T | 8 | a0001c0001t0001g0323 a0001c0001t0005g0218 a0001c0002t0001g0215 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.315-4302G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572094 | |||||||
| chr3:31572231 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.315-4165A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572231 | |||||||
| chr3:31572476 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.315-3920C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572476 | |||||||
| chr3:31572662 | G | C | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.315-3734G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572662 | |||||||
| chr3:31572779 | T | G | 1 | a0001c0001t0001g0301 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.315-3617T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572779 | |||||||
| chr3:31572820 | G | A | 8 | a0001c0001t0001g0323 a0001c0001t0005g0218 a0001c0002t0001g0215 others(5): Show |
8 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.315-3576G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572820 | |||||||
| chr3:31572843 | G | A | 4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0293 others(1): Show |
4 | HG02015.hp2 NA18968.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-3553G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572843 | |||||||
| chr3:31573048 | A | T | 1 | a0001c0001t0002g0060 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.315-3348A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573048 | |||||||
| chr3:31573099 | G | A | 115 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.315-3297G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573099 | |||||||
| chr3:31573400 | A | G | 1 | a0001c0001t0003g0012 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.315-2996A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573400 | |||||||
| chr3:31573442 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-2954G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573442 | |||||||
| chr3:31573532 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.315-2864A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573532 | |||||||
| chr3:31573572 | T | C | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.315-2824T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573572 | |||||||
| chr3:31573701 | A | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-2695A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573701 | |||||||
| chr3:31573855 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.315-2541A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573855 | |||||||
| chr3:31573915 | G | A | 13 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0023 others(10): Show |
14 | NA18946.hp1 NA18954.hp2 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.315-2481G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573915 | |||||||
| chr3:31574243 | T | C | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-2153T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31574243 | |||||||
| chr3:31574290 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(95): Show |
105 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.315-2106T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31574290 | |||||||
| chr3:31574504 | C | T | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG01167.hp1 HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.315-1892C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31574504 | |||||||
| chr3:31574576 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.315-1820T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31574576 | |||||||
| chr3:31574590 | A | G | 22 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(19): Show |
22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.315-1806A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31574590 | |||||||
| chr3:31575181 | C | T | 20 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.315-1215C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31575181 | |||||||
| chr3:31575376 | G | A | 1 | a0001c0007t0001g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.315-1020G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31575376 | |||||||
| chr3:31575466 | T | G | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.315-930T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31575466 | |||||||
| chr3:31575467 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-929G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31575467 | |||||||
| chr3:31575468 | G | GT | 4 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0001g0319 others(1): Show |
4 | HG02615.hp1 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-928_315-927ins others(1): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31575468 | |||||||
| chr3:31575497 | T | C | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(2): Show |
5 | HG00733.hp1 HG01168.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-899T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31575497 | |||||||
| chr3:31576167 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-229A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31576167 | |||||||
| chr3:31576204 | G | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(104): Show |
113 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.315-192G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31576204 | |||||||
| chr3:31576220 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.315-176C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31576220 | |||||||
| chr3:31576233 | G | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.315-163G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31576233 | |||||||
| chr3:31576273 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.315-123G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31576273 | |||||||
| chr3:31576353 | A | G | 1 | a0001c0001t0002g0055 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.315-43A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31576353 | |||||||
| chr3:31577056 | A | G | 5 | a0001c0001t0004g0005 a0001c0001t0004g0094 a0001c0001t0004g0095 others(2): Show |
6 | HG00423.hp2 HG00621.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.423+552A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577056 | |||||||
| chr3:31577178 | C | T | 184 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.423+674C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577178 | |||||||
| chr3:31577243 | A | G | 1 | a0001c0009t0001g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.423+739A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577243 | |||||||
| chr3:31577317 | T | G | 22 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(19): Show |
22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.423+813T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577317 | |||||||
| chr3:31577492 | T | C | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.423+988T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577492 | |||||||
| chr3:31577643 | C | A | 6 | a0001c0001t0001g0283 a0001c0001t0001g0285 a0001c0001t0001g0319 others(3): Show |
6 | HG02145.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+1139C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577643 | |||||||
| chr3:31577745 | T | C | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+1241T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577745 | |||||||
| chr3:31577784 | T | C | 110 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.423+1280T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577784 | |||||||
| chr3:31578049 | G | A | 9 | a0001c0001t0003g0012 a0001c0001t0003g0201 a0001c0001t0003g0202 others(6): Show |
10 | HG00735.hp2 HG01123.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.423+1545G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31578049 | |||||||
| chr3:31578567 | T | TC | 64 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(61): Show |
67 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.424-1235dupC | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31578567 | ||||||
| chr3:31578630 | G | A | 178 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.424-1179G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31578630 | |||||||
| chr3:31578806 | C | T | 1 | a0001c0001t0002g0064 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.424-1003C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31578806 | |||||||
| chr3:31578823 | G | A | 5 | a0001c0001t0001g0113 a0001c0001t0001g0115 a0001c0001t0001g0146 others(2): Show |
5 | NA18962.hp1 NA18972.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-986G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31578823 | |||||||
| chr3:31578825 | AAAT | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.424-981_424-979del others(3): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31578825 | ||||||
| chr3:31578864 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.424-945A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31578864 | |||||||
| chr3:31579130 | C | T | 1 | a0001c0001t0003g0240 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.424-679C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579130 | |||||||
| chr3:31579185 | G | A | 1 | a0001c0001t0003g0012 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.424-624G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579185 | |||||||
| chr3:31579193 | A | C | 1 | a0001c0001t0001g0274 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.424-616A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579193 | |||||||
| chr3:31579262 | C | T | 1 | a0001c0001t0005g0218 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.424-547C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579262 | |||||||
| chr3:31579352 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.424-457A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579352 | |||||||
| chr3:31579477 | T | TA | 38 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(35): Show |
39 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.424-305dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | ||||||
| chr3:31579477 | T | TAA | 8 | a0001c0001t0001g0070 a0001c0001t0001g0078 a0001c0001t0001g0282 others(5): Show |
8 | HG00621.hp1 HG02165.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.424-306_424-305dup others(2): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | ||||||
| chr3:31579477 | T | TAAA | 22 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0152 others(19): Show |
23 | HG01496.hp2 HG01884.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.424-307_424-305dup others(3): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | ||||||
| chr3:31579477 | T | TAAAA | 65 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0013 others(62): Show |
71 | HG00544.hp2 HG00639.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.424-308_424-305dup others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | ||||||
| chr3:31579477 | T | TAAAAA | 15 | a0001c0001t0001g0214 a0001c0001t0001g0228 a0001c0001t0001g0245 others(12): Show |
15 | HG00423.hp1 HG00558.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.424-309_424-305dup others(5): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | ||||||
| chr3:31579477 | TA | T | 62 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(59): Show |
68 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.424-305delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | ||||||
| chr3:31579477 | TAA | T | 10 | a0001c0001t0001g0089 a0001c0001t0001g0097 a0001c0001t0001g0133 others(7): Show |
10 | HG02738.hp2 NA18959.hp1 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.424-306_424-305del others(2): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | ||||||
| chr3:31579477 | TAAAA | T | 44 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(41): Show |
47 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.424-308_424-305del others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | ||||||
| chr3:31579477 | TAAAAAAA others(6): Show |
T | 1 | a0001c0002t0001g0217 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.424-317_424-305del others(13): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | ||||||
| chr3:31579478 | A | T | 3 | a0001c0001t0001g0120 a0001c0004t0005g0017 a0001c0004t0005g0318 |
3 | HG00544.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.424-331A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579478 | |||||||
| chr3:31579600 | T | C | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.424-209T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579600 | |||||||
| chr3:31579654 | T | G | 4 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | NA18951.hp1 NA18951.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-155T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579654 | |||||||
| chr3:31579694 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.424-115A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579694 | |||||||
| chr3:31579699 | GC | G | 9 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(6): Show |
9 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.424-109delC | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579699 | |||||||
| chr3:31579736 | T | TAAA | 299 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(296): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.424-73_424-72insAA others(1): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579736 | |||||||
| chr3:31579778 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.424-31G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579778 | |||||||
| chr3:31580199 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.711+103G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31580199 | |||||||
| chr3:31580247 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.711+151A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31580247 | |||||||
| chr3:31580512 | T | C | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.711+416T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31580512 | |||||||
| chr3:31580652 | T | C | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+556T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31580652 | |||||||
| chr3:31580826 | G | C | 1 | a0001c0001t0001g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.711+730G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31580826 | |||||||
| chr3:31580923 | T | C | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.711+827T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31580923 | |||||||
| chr3:31581185 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.711+1089A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581185 | |||||||
| chr3:31581263 | A | G | 1 | a0001c0001t0002g0036 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.711+1167A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581263 | |||||||
| chr3:31581367 | C | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | HG01167.hp1 HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.711+1271C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581367 | |||||||
| chr3:31581386 | A | G | 20 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.711+1290A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581386 | |||||||
| chr3:31581655 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.711+1559T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581655 | |||||||
| chr3:31581874 | C | G | 1 | a0001c0001t0002g0049 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.711+1778C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581874 | |||||||
| chr3:31581897 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.711+1801A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581897 | |||||||
| chr3:31581909 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.711+1813C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581909 | |||||||
| chr3:31581972 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0313 a0001c0001t0001g0314 |
4 | HG00639.hp1 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+1876T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581972 | |||||||
| chr3:31582030 | C | T | 1 | a0001c0001t0008g0260 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.711+1934C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582030 | |||||||
| chr3:31582151 | A | AT | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.711+2062dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31582151 | ||||||
| chr3:31582300 | C | CT | 117 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.711+2218dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31582300 | ||||||
| chr3:31582359 | G | A | 8 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0175 others(5): Show |
8 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.711+2263G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582359 | |||||||
| chr3:31582394 | C | G | 20 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.711+2298C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582394 | |||||||
| chr3:31582407 | G | C | 1 | a0001c0001t0004g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.711+2311G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582407 | |||||||
| chr3:31582429 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.711+2333G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582429 | |||||||
| chr3:31582544 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.711+2448C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582544 | |||||||
| chr3:31582722 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.711+2626G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582722 | |||||||
| chr3:31582815 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.711+2719T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582815 | |||||||
| chr3:31583008 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.711+2912G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583008 | |||||||
| chr3:31583090 | C | T | 4 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0248 others(1): Show |
4 | HG00423.hp1 NA18946.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+2994C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583090 | |||||||
| chr3:31583097 | G | T | 1 | a0001c0001t0001g0111 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.711+3001G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583097 | |||||||
| chr3:31583194 | T | C | 1 | a0001c0001t0003g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.711+3098T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583194 | |||||||
| chr3:31583312 | A | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0101 a0001c0001t0001g0264 |
4 | NA18950.hp1 NA18980.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+3216A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583312 | |||||||
| chr3:31583380 | A | G | 4 | a0001c0001t0003g0202 a0001c0001t0003g0209 a0001c0001t0003g0210 others(1): Show |
4 | HG00735.hp2 HG01123.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+3284A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583380 | |||||||
| chr3:31583505 | T | C | 9 | a0001c0001t0003g0012 a0001c0001t0003g0201 a0001c0001t0003g0202 others(6): Show |
10 | HG00735.hp2 HG01123.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+3409T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583505 | |||||||
| chr3:31583515 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.711+3419G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583515 | |||||||
| chr3:31583779 | T | G | 11 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(8): Show |
11 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.711+3683T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583779 | |||||||
| chr3:31584082 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.711+3986G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584082 | |||||||
| chr3:31584135 | A | G | 1 | a0001c0001t0002g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.711+4039A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584135 | |||||||
| chr3:31584307 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.711+4211G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584307 | |||||||
| chr3:31584380 | C | G | 1 | a0001c0001t0002g0049 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.711+4284C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584380 | |||||||
| chr3:31584433 | A | G | 1 | a0001c0001t0003g0202 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.711+4337A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584433 | |||||||
| chr3:31584516 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.711+4420A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584516 | |||||||
| chr3:31584604 | T | C | 7 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.711+4508T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584604 | |||||||
| chr3:31584650 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.711+4554C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584650 | |||||||
| chr3:31584784 | C | T | 1 | a0001c0001t0002g0020 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.711+4688C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584784 | |||||||
| chr3:31585107 | A | ATAAGTAC others(10): Show |
1 | a0001c0001t0002g0026 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.711+5012_711+5028d others(19): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31585107 | ||||||
| chr3:31585108 | T | G | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.711+5012T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585108 | |||||||
| chr3:31585118 | G | C | 1 | a0001c0001t0001g0015 | 2 | NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.711+5022G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585118 | |||||||
| chr3:31585273 | G | A | 26 | a0001c0001t0004g0005 a0001c0001t0004g0094 a0001c0001t0004g0095 others(23): Show |
27 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.711+5177G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585273 | |||||||
| chr3:31585332 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.711+5236A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585332 | |||||||
| chr3:31585333 | C | A | 1 | a0001c0001t0001g0115 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.711+5237C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585333 | |||||||
| chr3:31585347 | C | A | 1 | a0001c0001t0001g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.711+5251C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585347 | |||||||
| chr3:31585375 | G | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0131 |
2 | NA18963.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.711+5279G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585375 | |||||||
| chr3:31585555 | GGTTTT | G | 10 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0323 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+5475_711+5479d others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31585555 | ||||||
| chr3:31585839 | T | G | 18 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(15): Show |
18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.711+5743T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585839 | |||||||
| chr3:31586097 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.711+6001C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586097 | |||||||
| chr3:31586287 | T | G | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.711+6191T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586287 | |||||||
| chr3:31586327 | G | GAAAT | 299 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(296): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.711+6233_711+6236d others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31586327 | ||||||
| chr3:31586527 | T | C | 2 | a0001c0004t0005g0017 a0001c0004t0005g0318 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.711+6431T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586527 | |||||||
| chr3:31586571 | G | T | 13 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0023 others(10): Show |
14 | NA18946.hp1 NA18954.hp2 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.711+6475G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586571 | |||||||
| chr3:31586847 | T | C | 299 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(296): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.711+6751T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586847 | |||||||
| chr3:31586870 | T | G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0122 a0001c0001t0001g0135 |
3 | HG00140.hp1 HG00280.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.711+6774T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586870 | |||||||
| chr3:31586923 | T | C | 5 | a0001c0001t0004g0191 a0001c0001t0004g0192 a0001c0001t0004g0193 others(2): Show |
5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.711+6827T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586923 | |||||||
| chr3:31587079 | A | C | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.711+6983A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587079 | |||||||
| chr3:31587230 | T | G | 1 | a0001c0001t0001g0301 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.711+7134T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587230 | |||||||
| chr3:31587235 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.711+7139A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587235 | |||||||
| chr3:31587255 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.711+7159T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587255 | |||||||
| chr3:31587267 | A | AAAAG | 119 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.711+7172_711+7175d others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31587267 | ||||||
| chr3:31587303 | A | T | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.711+7207A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587303 | |||||||
| chr3:31587309 | C | T | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.711+7213C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587309 | |||||||
| chr3:31587414 | T | A | 1 | a0001c0004t0005g0017 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.711+7318T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587414 | |||||||
| chr3:31587812 | T | A | 1 | a0001c0001t0001g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.711+7716T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587812 | |||||||
| chr3:31588042 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.711+7946G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588042 | |||||||
| chr3:31588046 | A | T | 5 | a0001c0001t0001g0283 a0001c0001t0001g0319 a0001c0001t0001g0320 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.711+7950A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588046 | |||||||
| chr3:31588096 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.711+8000C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588096 | |||||||
| chr3:31588215 | G | T | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.711+8119G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588215 | |||||||
| chr3:31588240 | G | T | 4 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+8144G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588240 | |||||||
| chr3:31588244 | G | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.711+8148G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588244 | |||||||
| chr3:31588244 | G | T | 1 | a0001c0001t0001g0121 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.711+8148G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588244 | |||||||
| chr3:31588265 | T | G | 1 | a0001c0001t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.711+8169T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588265 | |||||||
| chr3:31588457 | T | G | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.712-8341T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588457 | |||||||
| chr3:31588487 | ATGCAC | A | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-8309_712-8305d others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31588487 | ||||||
| chr3:31588822 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.712-7976G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588822 | |||||||
| chr3:31588923 | G | GT | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-7874dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31588923 | ||||||
| chr3:31588978 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.712-7820A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588978 | |||||||
| chr3:31589094 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.712-7704A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589094 | |||||||
| chr3:31589112 | G | C | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.712-7686G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589112 | |||||||
| chr3:31589386 | C | T | 2 | a0001c0004t0005g0017 a0001c0004t0005g0066 |
2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.712-7412C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589386 | |||||||
| chr3:31589555 | G | T | 191 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.712-7243G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589555 | |||||||
| chr3:31589650 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.712-7148A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589650 | |||||||
| chr3:31589684 | T | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.712-7114T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589684 | |||||||
| chr3:31589861 | A | G | 7 | a0001c0001t0002g0025 a0001c0001t0002g0040 a0001c0001t0002g0047 others(4): Show |
7 | HG03942.hp1 NA18612.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.712-6937A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589861 | |||||||
| chr3:31589890 | T | A | 1 | a0001c0001t0001g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.712-6908T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589890 | |||||||
| chr3:31589902 | A | G | 1 | a0001c0001t0004g0183 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.712-6896A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589902 | |||||||
| chr3:31590134 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.712-6664C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590134 | |||||||
| chr3:31590144 | C | G | 1 | a0001c0001t0001g0268 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.712-6654C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590144 | |||||||
| chr3:31590239 | G | C | 50 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(47): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.712-6559G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590239 | |||||||
| chr3:31590253 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.712-6545T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590253 | |||||||
| chr3:31590299 | A | G | 1 | a0001c0001t0002g0025 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.712-6499A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590299 | |||||||
| chr3:31590315 | C | T | 8 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0001t0004g0175 others(5): Show |
8 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.712-6483C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590315 | |||||||
| chr3:31590643 | A | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-6155A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590643 | |||||||
| chr3:31590701 | G | A | 1 | a0001c0001t0003g0297 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.712-6097G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590701 | |||||||
| chr3:31590925 | T | G | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.712-5873T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590925 | |||||||
| chr3:31591057 | T | G | 5 | a0001c0001t0004g0191 a0001c0001t0004g0192 a0001c0001t0004g0193 others(2): Show |
5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-5741T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591057 | |||||||
| chr3:31591170 | C | T | 1 | a0001c0001t0003g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.712-5628C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591170 | |||||||
| chr3:31591444 | C | T | 1 | a0001c0009t0001g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.712-5354C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591444 | |||||||
| chr3:31591509 | T | A | 1 | a0001c0009t0001g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.712-5289T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591509 | |||||||
| chr3:31591520 | C | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.712-5278C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591520 | |||||||
| chr3:31591540 | A | G | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-5258A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591540 | |||||||
| chr3:31591655 | C | G | 1 | a0001c0001t0001g0242 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.712-5143C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591655 | |||||||
| chr3:31591679 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.712-5119G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591679 | |||||||
| chr3:31591913 | G | A | 1 | a0001c0001t0001g0302 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.712-4885G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591913 | |||||||
| chr3:31591929 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): Show |
77 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.712-4869G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591929 | |||||||
| chr3:31592091 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.712-4707A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592091 | |||||||
| chr3:31592137 | G | A | 25 | a0001c0001t0004g0005 a0001c0001t0004g0094 a0001c0001t0004g0095 others(22): Show |
26 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.712-4661G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592137 | |||||||
| chr3:31592173 | A | G | 1 | a0001c0004t0005g0017 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.712-4625A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592173 | |||||||
| chr3:31592320 | G | A | 1 | a0001c0004t0005g0017 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.712-4478G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592320 | |||||||
| chr3:31592416 | CA | C | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.712-4380delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31592416 | ||||||
| chr3:31592428 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.712-4370T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592428 | |||||||
| chr3:31592524 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.712-4274A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592524 | |||||||
| chr3:31592629 | T | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.712-4169T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592629 | |||||||
| chr3:31592630 | A | G | 9 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0285 others(6): Show |
9 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.712-4168A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592630 | |||||||
| chr3:31592771 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.712-4027C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592771 | |||||||
| chr3:31592772 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.712-4026G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592772 | |||||||
| chr3:31592967 | C | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0285 a0001c0001t0001g0308 others(6): Show |
10 | HG00639.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.712-3831C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592967 | |||||||
| chr3:31592987 | G | A | 9 | a0001c0001t0003g0012 a0001c0001t0003g0201 a0001c0001t0003g0202 others(6): Show |
10 | HG00735.hp2 HG01123.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.712-3811G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592987 | |||||||
| chr3:31592996 | G | A | 15 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(12): Show |
15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.712-3802G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592996 | |||||||
| chr3:31592998 | G | T | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.712-3800G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592998 | |||||||
| chr3:31593045 | G | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
95 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.712-3753G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593045 | |||||||
| chr3:31593266 | TGTGA | T | 8 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0200 others(5): Show |
8 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.712-3529_712-3526d others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31593266 | ||||||
| chr3:31593384 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.712-3414C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593384 | |||||||
| chr3:31593730 | A | G | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.712-3068A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593730 | |||||||
| chr3:31593751 | T | TA | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-3047_712-3046i others(3): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593751 | |||||||
| chr3:31593752 | C | T | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-3046C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593752 | |||||||
| chr3:31593905 | T | C | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.712-2893T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593905 | |||||||
| chr3:31593953 | A | G | 1 | a0001c0007t0001g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.712-2845A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593953 | |||||||
| chr3:31593976 | T | C | 8 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0296 others(5): Show |
8 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.712-2822T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593976 | |||||||
| chr3:31594018 | T | C | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-2780T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594018 | |||||||
| chr3:31594040 | T | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0264 |
3 | NA18950.hp1 NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.712-2758T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594040 | |||||||
| chr3:31594059 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.712-2739C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594059 | |||||||
| chr3:31594084 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.712-2714A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594084 | |||||||
| chr3:31594135 | A | C | 22 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(19): Show |
22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.712-2663A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594135 | |||||||
| chr3:31594206 | T | C | 1 | a0001c0004t0005g0318 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.712-2592T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594206 | |||||||
| chr3:31594436 | G | GT | 7 | a0001c0001t0001g0086 a0001c0001t0001g0151 a0001c0001t0001g0292 others(4): Show |
7 | HG01993.hp2 HG02071.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-2349dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31594436 | ||||||
| chr3:31594436 | G | GTTT | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.712-2351_712-2349d others(5): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31594436 | ||||||
| chr3:31594534 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.712-2264A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594534 | |||||||
| chr3:31594618 | C | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.712-2180C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594618 | |||||||
| chr3:31594656 | G | A | 1 | a0001c0001t0003g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.712-2142G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594656 | |||||||
| chr3:31594722 | C | A | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-2076C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594722 | |||||||
| chr3:31594811 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.712-1987C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594811 | |||||||
| chr3:31594854 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.712-1944C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594854 | |||||||
| chr3:31595019 | T | G | 2 | a0001c0004t0005g0017 a0001c0004t0005g0066 |
2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.712-1779T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595019 | |||||||
| chr3:31595155 | G | T | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.712-1643G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595155 | |||||||
| chr3:31595315 | A | G | 1 | a0001c0001t0005g0218 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.712-1483A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595315 | |||||||
| chr3:31595354 | A | G | 75 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(72): Show |
80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.712-1444A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595354 | |||||||
| chr3:31595401 | G | A | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.712-1397G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595401 | |||||||
| chr3:31595408 | G | T | 307 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(304): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.712-1390G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595408 | |||||||
| chr3:31595433 | G | T | 1 | a0001c0001t0001g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.712-1365G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595433 | |||||||
| chr3:31595501 | T | G | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.712-1297T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595501 | |||||||
| chr3:31595557 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.712-1241A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595557 | |||||||
| chr3:31595745 | A | T | 22 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(19): Show |
22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.712-1053A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595745 | |||||||
| chr3:31595769 | C | T | 15 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(12): Show |
15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.712-1029C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595769 | |||||||
| chr3:31595972 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.712-826C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595972 | |||||||
| chr3:31596152 | G | A | 3 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0322 |
3 | HG02717.hp2 HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.712-646G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31596152 | |||||||
| chr3:31596295 | C | T | 1 | a0001c0001t0002g0028 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.712-503C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31596295 | |||||||
| chr3:31596456 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.712-342G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31596456 | |||||||
| chr3:31596486 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.712-312A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31596486 | |||||||
| chr3:31596490 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.712-308T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31596490 | |||||||
| chr3:31596771 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.712-27A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31596771 | |||||||
| chr3:31596870 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG01516.hp1 | splice_region_variant&intron_variant | LOW | c.777+7T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31596870 | |||||||
| chr3:31596872 | T | A | 1 | a0001c0001t0001g0309 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.777+9T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31596872 | |||||||
| chr3:31596902 | G | C | 26 | a0001c0001t0004g0005 a0001c0001t0004g0094 a0001c0001t0004g0095 others(23): Show |
27 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.777+39G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31596902 | |||||||
| chr3:31597182 | C | T | 7 | a0001c0001t0001g0323 a0001c0002t0001g0215 a0001c0002t0001g0216 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+319C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597182 | |||||||
| chr3:31597305 | G | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.777+442G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597305 | |||||||
| chr3:31597410 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+547G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597410 | |||||||
| chr3:31597527 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.777+664G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597527 | |||||||
| chr3:31597635 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.777+772A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597635 | |||||||
| chr3:31597749 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+886G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597749 | |||||||
| chr3:31597840 | A | AT | 57 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(54): Show |
61 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.777+979dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 31597840 | ||||||
| chr3:31597840 | A | ATT | 28 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(25): Show |
31 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.777+978_777+979dup others(2): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 31597840 | ||||||
| chr3:31597840 | A | T | 3 | a0001c0001t0003g0187 a0001c0001t0003g0188 a0001c0004t0005g0066 |
3 | HG01934.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.777+977A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597840 | |||||||
| chr3:31597843 | A | T | 144 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.777+980A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597843 | |||||||
| chr3:31597846 | T | A | 2 | a0001c0001t0001g0316 a0001c0001t0002g0047 |
2 | HG02630.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.777+983T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597846 | |||||||
| chr3:31597884 | G | A | 6 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0023 others(3): Show |
7 | NA18954.hp2 NA18959.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.777+1021G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597884 | |||||||
| chr3:31597940 | A | G | 8 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0296 others(5): Show |
8 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.777+1077A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597940 | |||||||
| chr3:31598079 | G | C | 17 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(14): Show |
17 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.777+1216G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31598079 | |||||||
| chr3:31598409 | T | TA | 22 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(19): Show |
22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.777+1548dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 31598409 | ||||||
| chr3:31598627 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.778-1733A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31598627 | |||||||
| chr3:31598713 | T | C | 22 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(19): Show |
22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.778-1647T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31598713 | |||||||
| chr3:31598735 | A | G | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-1625A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31598735 | |||||||
| chr3:31598755 | T | C | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.778-1605T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31598755 | |||||||
| chr3:31598812 | C | CT | 9 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0296 others(6): Show |
9 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.778-1534dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 31598812 | ||||||
| chr3:31598865 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-1495A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31598865 | |||||||
| chr3:31599105 | A | G | 201 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.778-1255A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31599105 | |||||||
| chr3:31599415 | C | A | 1 | a0001c0001t0001g0261 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.778-945C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31599415 | |||||||
| chr3:31599415 | C | G | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.778-945C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31599415 | |||||||
| chr3:31599437 | T | C | 4 | a0001c0001t0005g0218 a0001c0004t0005g0017 a0001c0004t0005g0066 others(1): Show |
4 | HG01934.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-923T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31599437 | |||||||
| chr3:31599605 | G | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.778-755G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31599605 | |||||||
| chr3:31599719 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.778-641G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31599719 | |||||||
| chr3:31600069 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-291T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31600069 | |||||||
| chr3:31600105 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.778-255A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31600105 | |||||||
| chr3:31600140 | C | T | 1 | a0001c0001t0004g0178 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.778-220C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31600140 | |||||||
| chr3:31600201 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.778-159G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31600201 | |||||||
| chr3:31600343 | C | A | 10 | a0001c0001t0004g0172 a0001c0001t0004g0173 a0001c0001t0004g0174 others(7): Show |
10 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.778-17C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31600343 | |||||||
| chr3:31600545 | A | T | 115 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.877+86A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31600545 | |||||||
| chr3:31600785 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.877+326T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31600785 | |||||||
| chr3:31600925 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.877+466C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31600925 | |||||||
| chr3:31600949 | A | G | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.877+490A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31600949 | |||||||
| chr3:31600978 | A | T | 1 | a0001c0001t0001g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.877+519A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31600978 | |||||||
| chr3:31601216 | C | T | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(45): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.877+757C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601216 | |||||||
| chr3:31601217 | G | A | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.877+758G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601217 | |||||||
| chr3:31601335 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.877+876T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601335 | |||||||
| chr3:31601553 | C | A | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+1094C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601553 | |||||||
| chr3:31601574 | T | C | 6 | a0001c0001t0003g0198 a0001c0001t0003g0200 a0001c0001t0003g0203 others(3): Show |
6 | HG02258.hp2 HG02451.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+1115T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601574 | |||||||
| chr3:31601623 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.877+1164G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601623 | |||||||
| chr3:31601642 | G | C | 5 | a0001c0001t0004g0191 a0001c0001t0004g0192 a0001c0001t0004g0193 others(2): Show |
5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1183G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601642 | |||||||
| chr3:31601784 | C | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.877+1325C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601784 | |||||||
| chr3:31602081 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.877+1622G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602081 | |||||||
| chr3:31602229 | G | A | 50 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(47): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.877+1770G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602229 | |||||||
| chr3:31602239 | A | G | 1 | a0001c0001t0003g0297 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.877+1780A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602239 | |||||||
| chr3:31602303 | C | CT | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.877+1855dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31602303 | ||||||
| chr3:31602320 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.877+1861A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602320 | |||||||
| chr3:31602660 | A | AT | 13 | a0001c0001t0001g0087 a0001c0001t0001g0113 a0001c0001t0001g0124 others(10): Show |
13 | HG01993.hp2 HG02145.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.877+2223dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31602660 | ||||||
| chr3:31602660 | A | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0120 a0001c0001t0001g0155 others(3): Show |
7 | HG00544.hp1 NA18965.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.877+2201A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602660 | |||||||
| chr3:31602660 | AT | A | 97 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(94): Show |
102 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.877+2223delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31602660 | ||||||
| chr3:31602660 | ATT | A | 59 | a0001c0001t0001g0016 a0001c0001t0001g0256 a0001c0001t0001g0279 others(56): Show |
60 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.877+2222_877+2223d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31602660 | ||||||
| chr3:31602660 | ATTT | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(64): Show |
72 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.877+2221_877+2223d others(5): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31602660 | ||||||
| chr3:31602793 | T | C | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.877+2334T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602793 | |||||||
| chr3:31602824 | C | G | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.877+2365C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602824 | |||||||
| chr3:31602833 | T | C | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.877+2374T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602833 | |||||||
| chr3:31602874 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.877+2415A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602874 | |||||||
| chr3:31602885 | T | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.877+2426T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602885 | |||||||
| chr3:31602905 | G | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.877+2446G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602905 | |||||||
| chr3:31603098 | T | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
6 | HG00673.hp1 HG02165.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+2639T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603098 | |||||||
| chr3:31603122 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.877+2663G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603122 | |||||||
| chr3:31603145 | T | C | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.877+2686T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603145 | |||||||
| chr3:31603155 | AAGTTT | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0153 |
3 | HG01358.hp2 HG02148.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.877+2701_877+2705d others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31603155 | ||||||
| chr3:31603251 | A | T | 314 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(311): Show |
332 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.877+2792A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603251 | |||||||
| chr3:31603330 | T | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.877+2871T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603330 | |||||||
| chr3:31603427 | T | G | 2 | a0001c0001t0004g0180 a0001c0001t0004g0181 |
2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.877+2968T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603427 | |||||||
| chr3:31603568 | T | TTG | 3 | a0001c0001t0003g0237 a0001c0001t0003g0239 a0001c0001t0003g0240 |
3 | HG01167.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.877+3111_877+3112d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31603568 | ||||||
| chr3:31603681 | A | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.877+3222A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603681 | |||||||
| chr3:31603723 | G | GTA | 50 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(47): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.877+3267_877+3268d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31603723 | ||||||
| chr3:31603769 | TA | T | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.877+3311delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603769 | |||||||
| chr3:31604056 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.877+3597T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604056 | |||||||
| chr3:31604069 | T | C | 51 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0001 others(48): Show |
54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.877+3610T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604069 | |||||||
| chr3:31604108 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.877+3649T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604108 | |||||||
| chr3:31604137 | G | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0261 |
2 | NA18975.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.877+3678G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604137 | |||||||
| chr3:31604192 | A | G | 201 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(198): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.877+3733A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604192 | |||||||
| chr3:31604227 | T | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.877+3768T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604227 | |||||||
| chr3:31604251 | C | G | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.877+3792C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604251 | |||||||
| chr3:31604283 | G | A | 28 | a0001c0001t0003g0187 a0001c0001t0003g0188 a0001c0001t0004g0005 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.877+3824G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604283 | |||||||
| chr3:31604637 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.877+4178T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604637 | |||||||
| chr3:31605018 | A | G | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.877+4559A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31605018 | |||||||
| chr3:31605031 | T | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.877+4572T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31605031 | |||||||
| chr3:31605501 | GGTGA | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
93 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.877+5045_877+5048d others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31605501 | ||||||
| chr3:31605772 | G | A | 25 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(22): Show |
25 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.877+5313G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31605772 | |||||||
| chr3:31605925 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.877+5466C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31605925 | |||||||
| chr3:31606215 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.877+5756A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31606215 | |||||||
| chr3:31606224 | G | A | 198 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.877+5765G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31606224 | |||||||
| chr3:31606501 | CA | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
92 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.877+6044delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31606501 | ||||||
| chr3:31606736 | C | T | 86 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
93 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.877+6277C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31606736 | |||||||
| chr3:31606815 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.877+6356A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31606815 | |||||||
| chr3:31606816 | G | C | 1 | a0001c0001t0001g0295 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.877+6357G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31606816 | |||||||
| chr3:31607214 | T | G | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.877+6755T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607214 | |||||||
| chr3:31607314 | C | A | 1 | a0001c0001t0001g0308 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.877+6855C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607314 | |||||||
| chr3:31607397 | C | G | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 |
3 | NA18945.hp1 NA18954.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.877+6938C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607397 | |||||||
| chr3:31607454 | A | G | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.877+6995A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607454 | |||||||
| chr3:31607489 | G | A | 2 | a0001c0004t0005g0017 a0001c0004t0005g0066 |
2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.877+7030G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607489 | |||||||
| chr3:31607622 | A | G | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.877+7163A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607622 | |||||||
| chr3:31607692 | A | G | 22 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(19): Show |
22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.877+7233A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607692 | |||||||
| chr3:31607752 | G | GGTT | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): Show |
210 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.877+7299_877+7301d others(5): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31607752 | ||||||
| chr3:31607758 | TGTG | T | 22 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(19): Show |
22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.877+7302_877+7304d others(5): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31607758 | ||||||
| chr3:31607761 | G | T | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(273): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.877+7302G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607761 | |||||||
| chr3:31607846 | C | T | 112 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.878-7259C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607846 | |||||||
| chr3:31608037 | G | A | 1 | a0001c0001t0001g0013 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.878-7068G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608037 | |||||||
| chr3:31608213 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(103): Show |
112 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.878-6892G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608213 | |||||||
| chr3:31608257 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.878-6848A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608257 | |||||||
| chr3:31608289 | G | T | 5 | a0001c0001t0001g0250 a0001c0001t0001g0255 a0001c0001t0001g0259 others(2): Show |
5 | NA18942.hp1 NA18948.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-6816G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608289 | |||||||
| chr3:31608350 | C | T | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.878-6755C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608350 | |||||||
| chr3:31608365 | A | C | 25 | a0001c0001t0004g0005 a0001c0001t0004g0094 a0001c0001t0004g0095 others(22): Show |
26 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.878-6740A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608365 | |||||||
| chr3:31608421 | GA | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(86): Show |
95 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.878-6681delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31608421 | ||||||
| chr3:31608520 | T | C | 2 | a0001c0004t0005g0017 a0001c0004t0005g0318 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.878-6585T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608520 | |||||||
| chr3:31608652 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.878-6453C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608652 | |||||||
| chr3:31608692 | A | G | 1 | a0001c0001t0002g0064 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.878-6413A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608692 | |||||||
| chr3:31608796 | C | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.878-6309C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608796 | |||||||
| chr3:31608830 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | NA18975.hp2 NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.878-6275G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608830 | |||||||
| chr3:31608901 | G | C | 1 | a0001c0001t0001g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.878-6204G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608901 | |||||||
| chr3:31608995 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.878-6110G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608995 | |||||||
| chr3:31609008 | A | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.878-6097A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609008 | |||||||
| chr3:31609016 | G | A | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.878-6089G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609016 | |||||||
| chr3:31609404 | A | G | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.878-5701A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609404 | |||||||
| chr3:31609767 | G | A | 1 | a0001c0001t0004g0172 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.878-5338G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609767 | |||||||
| chr3:31609795 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(69): Show |
77 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.878-5310G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609795 | |||||||
| chr3:31609843 | G | A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.878-5262G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609843 | |||||||
| chr3:31609866 | C | T | 2 | a0001c0001t0004g0180 a0001c0001t0004g0181 |
2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.878-5239C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609866 | |||||||
| chr3:31609877 | A | G | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.878-5228A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609877 | |||||||
| chr3:31610036 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878-5069T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31610036 | |||||||
| chr3:31610394 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.878-4711G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31610394 | |||||||
| chr3:31610416 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.878-4689C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31610416 | |||||||
| chr3:31610480 | C | CTGCAA | 118 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.878-4621_878-4617d others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31610480 | ||||||
| chr3:31610523 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.878-4582G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31610523 | |||||||
| chr3:31610543 | A | G | 2 | a0001c0001t0003g0297 a0001c0004t0005g0318 |
2 | HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.878-4562A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31610543 | |||||||
| chr3:31610806 | C | T | 1 | a0001c0001t0003g0236 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.878-4299C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31610806 | |||||||
| chr3:31611062 | G | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.878-4043G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611062 | |||||||
| chr3:31611435 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.878-3670A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611435 | |||||||
| chr3:31611470 | C | T | 1 | a0001c0004t0005g0017 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.878-3635C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611470 | |||||||
| chr3:31611486 | G | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
96 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.878-3619G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611486 | |||||||
| chr3:31611530 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.878-3575G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611530 | |||||||
| chr3:31611744 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878-3361G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611744 | |||||||
| chr3:31611745 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0264 |
3 | NA18950.hp1 NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.878-3360C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611745 | |||||||
| chr3:31612546 | A | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.878-2559A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31612546 | |||||||
| chr3:31612567 | A | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.878-2538A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31612567 | |||||||
| chr3:31612734 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.878-2371G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31612734 | |||||||
| chr3:31612914 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878-2191T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31612914 | |||||||
| chr3:31612964 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0110 |
3 | HG02896.hp1 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.878-2141T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31612964 | |||||||
| chr3:31612974 | A | G | 10 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.878-2131A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31612974 | |||||||
| chr3:31613062 | T | G | 2 | a0001c0001t0005g0218 a0001c0004t0005g0017 |
2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.878-2043T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613062 | |||||||
| chr3:31613103 | G | A | 2 | a0001c0001t0005g0218 a0001c0004t0005g0017 |
2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.878-2002G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613103 | |||||||
| chr3:31613106 | G | A | 10 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.878-1999G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613106 | |||||||
| chr3:31613134 | G | T | 10 | a0001c0001t0004g0172 a0001c0001t0004g0173 a0001c0001t0004g0174 others(7): Show |
10 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.878-1971G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613134 | |||||||
| chr3:31613158 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.878-1947C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613158 | |||||||
| chr3:31613159 | G | A | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.878-1946G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613159 | |||||||
| chr3:31613194 | A | G | 20 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.878-1911A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613194 | |||||||
| chr3:31613200 | A | G | 22 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(19): Show |
22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.878-1905A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613200 | |||||||
| chr3:31613274 | C | A | 1 | a0001c0004t0005g0017 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.878-1831C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613274 | |||||||
| chr3:31613283 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.878-1822G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613283 | |||||||
| chr3:31613459 | C | G | 1 | a0001c0001t0001g0229 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.878-1646C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613459 | |||||||
| chr3:31613624 | C | G | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.878-1481C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613624 | |||||||
| chr3:31613667 | CT | C | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.878-1428delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31613667 | ||||||
| chr3:31613676 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.878-1429T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613676 | |||||||
| chr3:31613761 | C | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0283 a0001c0001t0001g0285 others(11): Show |
15 | HG00639.hp1 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.878-1344C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613761 | |||||||
| chr3:31613927 | G | A | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.878-1178G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613927 | |||||||
| chr3:31614018 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878-1087T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614018 | |||||||
| chr3:31614027 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878-1078A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614027 | |||||||
| chr3:31614150 | C | T | 89 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(86): Show |
95 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.878-955C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614150 | |||||||
| chr3:31614172 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878-933C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614172 | |||||||
| chr3:31614173 | G | C | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0121 others(1): Show |
4 | NA18612.hp2 NA18944.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.878-932G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614173 | |||||||
| chr3:31614362 | C | T | 2 | a0001c0004t0005g0017 a0001c0004t0005g0066 |
2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.878-743C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614362 | |||||||
| chr3:31614467 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0114 a0001c0001t0001g0131 others(1): Show |
5 | NA18963.hp2 NA18968.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-638C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614467 | |||||||
| chr3:31614721 | C | CAT | 191 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.878-384_878-383ins others(2): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614721 | |||||||
| chr3:31614726 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.878-379A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614726 | |||||||
| chr3:31614770 | GT | G | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.878-334delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614770 | |||||||
| chr3:31615050 | T | G | 1 | a0001c0009t0001g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.878-55T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31615050 | |||||||
| chr3:31615283 | T | G | 1 | a0001c0001t0001g0259 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.976+80T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615283 | |||||||
| chr3:31615347 | G | C | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.976+144G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615347 | |||||||
| chr3:31615480 | T | A | 1 | a0001c0001t0001g0259 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.976+277T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615480 | |||||||
| chr3:31615509 | G | A | 20 | a0001c0001t0004g0005 a0001c0001t0004g0094 a0001c0001t0004g0095 others(17): Show |
21 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(18): Show |
intron_variant | MODIFIER | c.976+306G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615509 | |||||||
| chr3:31615593 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.976+390C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615593 | |||||||
| chr3:31615710 | G | A | 25 | a0001c0001t0004g0005 a0001c0001t0004g0094 a0001c0001t0004g0095 others(22): Show |
26 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.976+507G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615710 | |||||||
| chr3:31615929 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0313 a0001c0001t0001g0314 |
4 | HG00639.hp1 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.976+726A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615929 | |||||||
| chr3:31615945 | ACTC | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.976+745_976+747del others(3): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 31615945 | ||||||
| chr3:31616211 | G | T | 1 | a0001c0001t0002g0036 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.977-718G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31616211 | |||||||
| chr3:31616290 | A | T | 1 | a0001c0001t0001g0259 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.977-639A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31616290 | |||||||
| chr3:31616376 | C | CT | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.977-551dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 31616376 | ||||||
| chr3:31616447 | A | G | 11 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(8): Show |
11 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.977-482A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31616447 | |||||||
| chr3:31616498 | T | C | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.977-431T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31616498 | |||||||
| chr3:31616772 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.977-157G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31616772 | |||||||
| chr3:31616861 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | NA19007.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.977-68C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31616861 | |||||||
| chr3:31617186 | C | CT | 27 | a0001c0001t0001g0114 a0001c0001t0001g0119 a0001c0001t0004g0005 others(24): Show |
28 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.1123+126dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 31617186 | ||||||
| chr3:31617186 | C | CTT | 87 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(84): Show |
94 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1123+125_1123+126d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 31617186 | ||||||
| chr3:31617186 | CT | C | 47 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(44): Show |
50 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1123+126delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 31617186 | ||||||
| chr3:31617222 | G | T | 2 | a0001c0001t0003g0012 a0001c0001t0003g0212 |
3 | NA18948.hp2 NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1123+147G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | chr3 | 31617222 | |||||||
| chr3:31617429 | C | T | 2 | a0001c0001t0001g0284 a0001c0001t0001g0296 |
2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1123+354C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | chr3 | 31617429 | |||||||
| chr3:31617517 | G | T | 2 | a0001c0004t0005g0017 a0001c0004t0005g0066 |
2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1124-423G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | chr3 | 31617517 | |||||||
| chr3:31617846 | G | A | 1 | a0001c0001t0003g0209 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1124-94G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | chr3 | 31617846 | |||||||
| chr3:31618003 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1172+15A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618003 | |||||||
| chr3:31618011 | G | A | 1 | a0001c0004t0005g0017 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1172+23G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618011 | |||||||
| chr3:31618262 | T | C | 118 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1172+274T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618262 | |||||||
| chr3:31618287 | T | TTACCTAA others(2): Show |
298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1172+301_1172+302i others(11): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 31618287 | ||||||
| chr3:31618456 | T | G | 1 | a0001c0001t0001g0002 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1172+468T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618456 | |||||||
| chr3:31618469 | A | C | 1 | a0001c0001t0001g0296 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1172+481A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618469 | |||||||
| chr3:31618628 | G | C | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1172+640G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618628 | |||||||
| chr3:31618865 | T | C | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | NA18951.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1173-811T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618865 | |||||||
| chr3:31618937 | TTATAA | T | 18 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(15): Show |
18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1173-733_1173-729d others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 31618937 | ||||||
| chr3:31619040 | C | T | 1 | a0001c0004t0005g0017 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1173-636C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31619040 | |||||||
| chr3:31619261 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1173-415T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31619261 | |||||||
| chr3:31619851 | A | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1327+21A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31619851 | |||||||
| chr3:31620132 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1327+302G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620132 | |||||||
| chr3:31620148 | G | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1327+318G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620148 | |||||||
| chr3:31620262 | G | A | 32 | a0001c0001t0001g0107 a0001c0001t0001g0118 a0001c0001t0001g0137 others(29): Show |
33 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1327+432G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620262 | |||||||
| chr3:31620274 | C | CAA | 73 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(70): Show |
78 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1327+460_1327+461d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 31620274 | ||||||
| chr3:31620274 | CA | C | 7 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(4): Show |
7 | HG01515.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1327+461delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 31620274 | ||||||
| chr3:31620277 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1327+447A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620277 | |||||||
| chr3:31620285 | A | G | 1 | a0001c0001t0005g0218 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1327+455A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620285 | |||||||
| chr3:31620349 | A | G | 2 | a0001c0004t0005g0017 a0001c0004t0005g0318 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1327+519A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620349 | |||||||
| chr3:31620356 | G | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1327+526G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620356 | |||||||
| chr3:31620365 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(72): Show |
80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1327+535G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620365 | |||||||
| chr3:31620417 | C | T | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1327+587C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620417 | |||||||
| chr3:31620560 | C | T | 298 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(295): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1327+730C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620560 | |||||||
| chr3:31620681 | G | T | 46 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(43): Show |
49 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1327+851G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620681 | |||||||
| chr3:31620865 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0308 a0001c0001t0001g0309 others(5): Show |
9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1327+1035T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620865 | |||||||
| chr3:31620892 | C | T | 2 | a0001c0004t0005g0017 a0001c0004t0005g0066 |
2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1327+1062C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620892 | |||||||
| chr3:31620901 | TTCTCTAG others(1): Show |
T | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(45): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1327+1073_1327+108 others(12): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 31620901 | ||||||
| chr3:31621148 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1328-949A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31621148 | |||||||
| chr3:31621583 | A | G | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1328-514A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31621583 | |||||||
| chr3:31621655 | A | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0268 |
2 | NA18964.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1328-442A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31621655 | |||||||
| chr3:31621676 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1328-421G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31621676 | |||||||
| chr3:31621711 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1328-386G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31621711 | |||||||
| chr3:31621984 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1328-113C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31621984 | |||||||
| chr3:31622013 | T | C | 1 | a0001c0001t0002g0063 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1328-84T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31622013 | |||||||
| chr3:31622377 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1539+69C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31622377 | |||||||
| chr3:31622679 | C | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(104): Show |
113 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1539+371C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31622679 | |||||||
| chr3:31622807 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1539+499G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31622807 | |||||||
| chr3:31622896 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1539+588G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31622896 | |||||||
| chr3:31622933 | G | A | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1539+625G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31622933 | |||||||
| chr3:31623023 | T | A | 1 | a0001c0001t0001g0155 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1540-651T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31623023 | |||||||
| chr3:31623156 | TG | T | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1540-517delG | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31623156 | |||||||
| chr3:31623226 | G | A | 82 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
89 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.1540-448G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31623226 | |||||||
| chr3:31623281 | A | G | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1540-393A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31623281 | |||||||
| chr3:31623354 | A | C | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1540-320A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31623354 | |||||||
| chr3:31623913 | G | A | 4 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | NA18951.hp1 NA18951.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1727+52G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31623913 | |||||||
| chr3:31624077 | G | A | 10 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0305 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1727+216G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624077 | |||||||
| chr3:31624088 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1727+227G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624088 | |||||||
| chr3:31624221 | C | T | 1 | a0001c0002t0001g0220 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1727+360C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624221 | |||||||
| chr3:31624231 | C | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0031 |
2 | NA18942.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1727+370C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624231 | |||||||
| chr3:31624236 | G | T | 3 | a0001c0004t0005g0017 a0001c0004t0005g0066 a0001c0004t0005g0318 |
3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1727+375G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624236 | |||||||
| chr3:31624295 | T | C | 2 | a0001c0004t0005g0017 a0001c0004t0005g0318 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1727+434T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624295 | |||||||
| chr3:31624667 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1728-247C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624667 | |||||||
| chr3:31624670 | CT | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0013 others(124): Show |
136 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1728-227delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 31624670 | ||||||
| chr3:31624749 | C | T | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1728-165C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624749 | |||||||
| chr3:31624764 | CT | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(71): Show |
79 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1728-140delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 31624764 | ||||||
| chr3:31624865 | C | A | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1728-49C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624865 | |||||||
| chr3:31625118 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1899+33C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 12/15 | chr3 | 31625118 | |||||||
| chr3:31625186 | C | T | 1 | a0001c0009t0001g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1899+101C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 12/15 | chr3 | 31625186 | |||||||
| chr3:31625799 | A | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(296): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1900-155A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 12/15 | chr3 | 31625799 | |||||||
| chr3:31626141 | T | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0120 a0001c0001t0001g0155 others(3): Show |
7 | HG00544.hp1 NA18965.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.2073+14T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31626141 | |||||||
| chr3:31626625 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2073+498G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31626625 | |||||||
| chr3:31626668 | G | T | 1 | a0001c0001t0004g0194 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2073+541G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31626668 | |||||||
| chr3:31626763 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2073+636A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31626763 | |||||||
| chr3:31626808 | A | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(75): Show |
83 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.2073+681A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31626808 | |||||||
| chr3:31627235 | C | G | 1 | a0001c0004t0005g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2073+1108C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627235 | |||||||
| chr3:31627268 | T | C | 299 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(296): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.2073+1141T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627268 | |||||||
| chr3:31627597 | G | A | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG00558.hp1 NA19065.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2073+1470G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627597 | |||||||
| chr3:31627694 | G | A | 20 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.2073+1567G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627694 | |||||||
| chr3:31627722 | C | T | 1 | a0001c0001t0001g0009 | 2 | NA18977.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2074-1576C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627722 | |||||||
| chr3:31627802 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2074-1496A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627802 | |||||||
| chr3:31627830 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2074-1468C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627830 | |||||||
| chr3:31628011 | T | TA | 112 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.2074-1275dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 31628011 | ||||||
| chr3:31628011 | T | TAA | 6 | a0001c0001t0001g0011 a0001c0001t0001g0108 a0001c0001t0001g0150 others(3): Show |
7 | HG00639.hp2 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.2074-1276_2074-127 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 31628011 | ||||||
| chr3:31628219 | T | TG | 58 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0073 others(55): Show |
58 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.2074-1072dupG | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 31628219 | ||||||
| chr3:31628306 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2074-992C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31628306 | |||||||
| chr3:31628455 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2074-843C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31628455 | |||||||
| chr3:31628495 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2074-803G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31628495 | |||||||
| chr3:31628526 | T | C | 13 | a0001c0001t0001g0283 a0001c0001t0001g0285 a0001c0001t0001g0315 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2074-772T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31628526 | |||||||
| chr3:31628819 | T | C | 8 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0200 others(5): Show |
8 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2074-479T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31628819 | |||||||
| chr3:31628997 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2074-301T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31628997 | |||||||
| chr3:31629066 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2074-232A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31629066 | |||||||
| chr3:31629186 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2074-112C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31629186 | |||||||
| chr3:31629514 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2187+103A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629514 | |||||||
| chr3:31629594 | A | G | 9 | a0001c0001t0003g0012 a0001c0001t0003g0201 a0001c0001t0003g0202 others(6): Show |
10 | HG00735.hp2 HG01123.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.2187+183A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629594 | |||||||
| chr3:31629645 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2187+234A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629645 | |||||||
| chr3:31629719 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2187+308C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629719 | |||||||
| chr3:31629779 | A | C | 1 | a0001c0001t0002g0036 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2187+368A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629779 | |||||||
| chr3:31629807 | T | A | 1 | a0001c0001t0001g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2187+396T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629807 | |||||||
| chr3:31629831 | T | C | 3 | a0001c0001t0005g0218 a0001c0004t0005g0017 a0001c0004t0005g0318 |
3 | HG03139.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2187+420T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629831 | |||||||
| chr3:31629861 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2187+450T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629861 | |||||||
| chr3:31630209 | A | G | 1 | a0001c0001t0002g0056 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2187+798A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630209 | |||||||
| chr3:31630250 | C | T | 1 | a0001c0001t0004g0176 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2187+839C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630250 | |||||||
| chr3:31630665 | G | A | 191 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.2187+1254G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630665 | |||||||
| chr3:31630725 | A | G | 7 | a0001c0001t0001g0323 a0001c0002t0001g0215 a0001c0002t0001g0216 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2187+1314A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630725 | |||||||
| chr3:31630795 | GT | G | 190 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.2187+1392delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 31630795 | ||||||
| chr3:31630796 | T | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(76): Show |
84 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.2187+1385T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630796 | |||||||
| chr3:31630803 | T | G | 1 | a0001c0010t0002g0044 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2187+1392T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630803 | |||||||
| chr3:31630804 | G | GT | 6 | a0001c0001t0001g0255 a0001c0001t0001g0283 a0001c0001t0001g0287 others(3): Show |
6 | HG00738.hp1 HG03195.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.2187+1403dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 31630804 | ||||||
| chr3:31630804 | G | T | 1 | a0001c0010t0002g0044 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2187+1393G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630804 | |||||||
| chr3:31630828 | G | T | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2187+1417G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630828 | |||||||
| chr3:31630835 | C | T | 1 | a0001c0001t0002g0026 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2187+1424C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630835 | |||||||
| chr3:31631017 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2187+1606C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31631017 | |||||||
| chr3:31631039 | T | C | 1 | a0001c0001t0004g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2187+1628T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31631039 | |||||||
| chr3:31631078 | C | T | 2 | a0001c0001t0005g0218 a0001c0004t0005g0017 |
2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2187+1667C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31631078 | |||||||
| chr3:31631583 | T | A | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2188-1352T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31631583 | |||||||
| chr3:31631781 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2188-1154G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31631781 | |||||||
| chr3:31631978 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(76): Show |
84 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.2188-957C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31631978 | |||||||
| chr3:31632082 | C | CT | 49 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(46): Show |
52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2188-852dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 31632082 | ||||||
| chr3:31632098 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2188-837C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632098 | |||||||
| chr3:31632226 | C | T | 14 | a0001c0001t0002g0001 a0001c0001t0002g0018 a0001c0001t0002g0024 others(11): Show |
16 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.2188-709C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632226 | |||||||
| chr3:31632549 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2188-386C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632549 | |||||||
| chr3:31632669 | GT | G | 103 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(100): Show |
107 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.2188-250delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 31632669 | ||||||
| chr3:31632669 | GTT | G | 88 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(85): Show |
94 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.2188-251_2188-250d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 31632669 | ||||||
| chr3:31632670 | T | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(74): Show |
82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.2188-265T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632670 | |||||||
| chr3:31632671 | T | G | 1 | a0001c0001t0001g0289 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2188-264T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632671 | |||||||
| chr3:31632673 | T | G | 26 | a0001c0001t0004g0005 a0001c0001t0004g0094 a0001c0001t0004g0095 others(23): Show |
27 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.2188-262T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632673 | |||||||
| chr3:31632763 | A | G | 4 | a0001c0001t0001g0242 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | NA18964.hp2 NA18965.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.2188-172A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632763 | |||||||
| chr3:31633276 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0087 a0001c0001t0001g0088 others(1): Show |
5 | HG00733.hp2 HG02145.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.2400+129G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633276 | |||||||
| chr3:31633316 | A | C | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2400+169A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633316 | |||||||
| chr3:31633422 | T | C | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.2400+275T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633422 | |||||||
| chr3:31633481 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 |
3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2400+334G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633481 | |||||||
| chr3:31633615 | TA | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(104): Show |
113 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.2400+469delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633615 | |||||||
| chr3:31633671 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2400+524A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633671 | |||||||
| chr3:31633686 | T | G | 1 | a0001c0001t0001g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2400+539T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633686 | |||||||
| chr3:31633769 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2400+622C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633769 | |||||||
| chr3:31634043 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2400+896G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634043 | |||||||
| chr3:31634174 | G | C | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.2400+1027G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634174 | |||||||
| chr3:31634655 | C | T | 50 | a0001c0001t0001g0309 a0001c0001t0002g0001 a0001c0001t0002g0003 others(47): Show |
53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.2401-1329C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634655 | |||||||
| chr3:31634676 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2401-1308A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634676 | |||||||
| chr3:31634805 | T | A | 1 | a0001c0009t0001g0171 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2401-1179T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634805 | |||||||
| chr3:31634848 | A | G | 28 | a0001c0001t0003g0187 a0001c0001t0003g0188 a0001c0001t0004g0005 others(25): Show |
29 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.2401-1136A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634848 | |||||||
| chr3:31634876 | C | A | 21 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(18): Show |
21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.2401-1108C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634876 | |||||||
| chr3:31635048 | A | G | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 |
3 | NA18945.hp1 NA18954.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.2401-936A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635048 | |||||||
| chr3:31635134 | C | T | 1 | a0001c0007t0001g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2401-850C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635134 | |||||||
| chr3:31635221 | A | G | 2 | a0001c0004t0005g0017 a0001c0004t0005g0318 |
2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2401-763A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635221 | |||||||
| chr3:31635252 | A | G | 20 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(17): Show |
20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.2401-732A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635252 | |||||||
| chr3:31635435 | T | C | 1 | a0001c0001t0002g0047 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2401-549T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635435 | |||||||
| chr3:31635458 | T | G | 1 | a0001c0001t0001g0301 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2401-526T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635458 | |||||||
| chr3:31635536 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2401-448A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635536 | |||||||
| chr3:31635567 | C | G | 4 | a0001c0003t0001g0222 a0001c0003t0001g0223 a0001c0003t0001g0224 others(1): Show |
4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2401-417C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635567 | |||||||
| chr3:31635569 | A | G | 1 | a0001c0001t0003g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2401-415A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635569 | |||||||
| chr3:31635632 | G | C | 1 | a0001c0001t0001g0101 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2401-352G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635632 | |||||||
| chr3:31635898 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2401-86A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635898 | |||||||
| chr3:31635903 | T | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(296): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.2401-81T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635903 | |||||||
| chr3:31635940 | A | G | 48 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0018 others(45): Show |
51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.2401-44A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635940 |