Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79703 |
| ensemblid | ENSG00000173715.19 |
| hgncid | 26197 |
| symbol | C11orf80 |
| name | TOP6B like initiator of meiotic double strand breaks |
| refseq_nuc | NM_001302084.2 |
| refseq_prot | NP_001289013.1 |
| ensembl_nuc | ENST00000540737.7 |
| ensembl_prot | ENSP00000444319.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 66744769 |
| end | 66843516 |
| strand | + |
| ver | v1.2 |
| region | chr11:66744769-66843516 |
| region5000 | chr11:66739769-66848516 |
| regionname0 | C11orf80_chr11_66744769_66843516 |
| regionname5000 | C11orf80_chr11_66739769_66848516 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 511 | 237 | 56 | 30 | 119 | 10 | 20 | 92 | C11orf80_chr11_66739769_66848516 | C11orf80 | MVLKK others(506): Show |
chr11 | 66739769 | 66848516 |
| a0002 | 0/0 | 511 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | MVLKK others(506): Show |
chr11 | 66739769 | 66848516 |
| a0003 | 0/0 | 511 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | MVLKK others(506): Show |
chr11 | 66739769 | 66848516 |
| a0004 | 0/0 | 511 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | MVLKK others(506): Show |
chr11 | 66739769 | 66848516 |
| a0005 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | MVLKK others(506): Show |
chr11 | 66739769 | 66848516 |
| a0006 | 0/0 | 511 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | MVLKK others(506): Show |
chr11 | 66739769 | 66848516 |
| a0007 | 0/0 | 511 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | MVLKK others(506): Show |
chr11 | 66739769 | 66848516 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1533 | 188 | 43 | 20 | 101 | 7 | 16 | C11orf80_chr11_66739769_66848516 | C11orf80 | ATGGT others(1528): Show |
chr11 | 66739769 | 66848516 | ||
| a0001c0002 | 0/1 | 1533 | 48 | 12 | 10 | 18 | 3 | 4 | C11orf80_chr11_66739769_66848516 | C11orf80 | ATGGT others(1528): Show |
chr11 | 66739769 | 66848516 | ||
| a0001c0007 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | ATGGT others(1528): Show |
chr11 | 66739769 | 66848516 | ||
| a0002c0003 | 0/0 | 1533 | 4 | 3 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | ATGGT others(1528): Show |
chr11 | 66739769 | 66848516 | ||
| a0003c0004 | 0/0 | 1533 | 2 | 1 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | ATGGT others(1528): Show |
chr11 | 66739769 | 66848516 | ||
| a0004c0005 | 0/0 | 1533 | 2 | 2 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | ATGGT others(1528): Show |
chr11 | 66739769 | 66848516 | ||
| a0005c0008 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | ATGGT others(1528): Show |
chr11 | 66739769 | 66848516 | ||
| a0006c0009 | 0/0 | 1533 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | ATGGT others(1528): Show |
chr11 | 66739769 | 66848516 | ||
| a0007c0006 | 0/0 | 1533 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | ATGGT others(1528): Show |
chr11 | 66739769 | 66848516 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1998 | 92 | 17 | 5 | 61 | 2 | 6 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1993): Show |
chr11 | 66739769 | 66848516 |
| a0001c0001t0002 | 0/0 | 2001 | 66 | 11 | 6 | 39 | 2 | 8 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1996): Show |
chr11 | 66739769 | 66848516 |
| a0001c0001t0003 | 0/0 | 2004 | 10 | 2 | 4 | 0 | 3 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1999): Show |
chr11 | 66739769 | 66848516 |
| a0001c0001t0004 | 0/0 | 1998 | 9 | 8 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1993): Show |
chr11 | 66739769 | 66848516 |
| a0001c0001t0006 | 0/0 | 2001 | 4 | 3 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1996): Show |
chr11 | 66739769 | 66848516 |
| a0001c0001t0007 | 0/0 | 2006 | 3 | 0 | 3 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(2001): Show |
chr11 | 66739769 | 66848516 |
| a0001c0001t0009 | 0/0 | 1993 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1988): Show |
chr11 | 66739769 | 66848516 |
| a0001c0001t0010 | 0/0 | 2013 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(2008): Show |
chr11 | 66739769 | 66848516 |
| a0001c0001t0011 | 0/0 | 2010 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(2005): Show |
chr11 | 66739769 | 66848516 |
| a0001c0001t0012 | 0/0 | 2004 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1999): Show |
chr11 | 66739769 | 66848516 |
| a0001c0002t0001 | 0/1 | 1998 | 43 | 11 | 8 | 17 | 2 | 4 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1993): Show |
chr11 | 66739769 | 66848516 |
| a0001c0002t0002 | 0/0 | 2001 | 4 | 1 | 1 | 1 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1996): Show |
chr11 | 66739769 | 66848516 |
| a0001c0002t0013 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1993): Show |
chr11 | 66739769 | 66848516 |
| a0001c0007t0004 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1993): Show |
chr11 | 66739769 | 66848516 |
| a0002c0003t0005 | 0/0 | 1993 | 4 | 3 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1988): Show |
chr11 | 66739769 | 66848516 |
| a0003c0004t0008 | 0/0 | 1996 | 2 | 1 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1991): Show |
chr11 | 66739769 | 66848516 |
| a0004c0005t0005 | 0/0 | 1993 | 2 | 2 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1988): Show |
chr11 | 66739769 | 66848516 |
| a0005c0008t0002 | 0/0 | 2001 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1996): Show |
chr11 | 66739769 | 66848516 |
| a0006c0009t0001 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1993): Show |
chr11 | 66739769 | 66848516 |
| a0007c0006t0009 | 0/0 | 1993 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | GTGGA others(1988): Show |
chr11 | 66739769 | 66848516 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0007g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0007g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0007g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0010g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0011g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0001t0012g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0002t0013g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0001c0007t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0002c0003t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0002c0003t0005g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0002c0003t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0002c0003t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0003c0004t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0003c0004t0008g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0004c0005t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0004c0005t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0005c0008t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0006c0009t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| a0007c0006t0009g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0150 | EUR | GBR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0073 | EUR | GBR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0044 | EUR | FIN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0011 | EUR | FIN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0181 | EUR | FIN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0192 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01109 | hp2 | a0003 | c0004 | t0008 | g0063 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01168 | hp1 | a0001 | c0002 | t0013 | g0071 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0226 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0228 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01243 | hp1 | a0002 | c0003 | t0005 | g0120 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0081 | AMR | PUR | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0198 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0137 | EUR | IBS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01884 | hp1 | a0002 | c0003 | t0005 | g0118 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | PEL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0089 | AMR | PEL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PEL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0064 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02071 | hp2 | a0001 | c0001 | t0011 | g0233 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CDX | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CDX | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02615 | hp2 | a0002 | c0003 | t0005 | g0237 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0082 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02647 | hp1 | a0004 | c0005 | t0005 | g0119 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0194 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0085 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0135 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0087 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0021 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03098 | hp1 | a0003 | c0004 | t0008 | g0062 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03195 | hp2 | a0005 | c0008 | t0002 | g0165 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03225 | hp2 | a0002 | c0003 | t0005 | g0238 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0065 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03516 | hp2 | a0001 | c0007 | t0004 | g0188 | AFR | ESN | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03540 | hp2 | a0001 | c0001 | t0010 | g0088 | AFR | GWD | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03654 | hp1 | a0001 | c0001 | t0012 | g0144 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | YRI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | CHB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18747 | hp2 | a0006 | c0009 | t0001 | g0008 | EAS | CHB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18906 | hp1 | a0004 | c0005 | t0005 | g0236 | AFR | YRI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | LWK | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0067 | AFR | LWK | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | YRI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | TSI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0211 | EUR | TSI | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01123 | hp1 | a0001 | c0001 | t0007 | g0227 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | CLM | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG03471 | hp2 | a0001 | c0001 | t0009 | g0004 | AFR | MSL | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | USA | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | USA | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | LWK | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| NA21309 | hp2 | a0007 | c0006 | t0009 | g0247 | AFR | LWK | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0195 | REF | REF | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0241 | REF | REF | C11orf80_chr11_66739769_66848516 | C11orf80 | chr11 | 66739769 | 66848516 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:66788262 | T | C | 1 | a0003 | 2 | HG01109.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.128T>C | p.Ile43Thr | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/15 | 308/1998 | 128/1536 | 43/511 | chr11 | 66788262 | |||
| chr11:66801077 | T | G | 2 | a0002 a0004 |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
missense_variant | MODERATE | c.322T>G | p.Leu108Val | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/15 | 502/1998 | 322/1536 | 108/511 | chr11 | 66801077 | |||
| chr11:66804173 | A | G | 1 | a0006 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.526A>G | p.Arg176Gly | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/15 | 706/1998 | 526/1536 | 176/511 | chr11 | 66804173 | |||
| chr11:66813980 | G | A | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.659G>A | p.Cys220Tyr | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/15 | 839/1998 | 659/1536 | 220/511 | chr11 | 66813980 | |||
| chr11:66813986 | T | C | 1 | a0004 | 2 | HG02647.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.665T>C | p.Ile222Thr | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/15 | 845/1998 | 665/1536 | 222/511 | chr11 | 66813986 | |||
| chr11:66838419 | A | T | 1 | a0005 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.1223A>T | p.Asp408Val | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/15 | 1403/1998 | 1223/1536 | 408/511 | chr11 | 66838419 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:66838438 | C | T | 1 | a0003c0004 | 2 | HG01109.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.1242C>T | p.Leu414Leu | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/15 | 1422/1998 | 1242/1536 | 414/511 | chr11 | 66838438 | |||
| chr11:66843021 | C | T | 1 | a0001c0007 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1422C>T | p.His474His | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 14/15 | 1602/1998 | 1422/1536 | 474/511 | chr11 | 66843021 | |||
| chr11:66843174 | G | C | 1 | a0001c0002 | 47 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(44): Show |
synonymous_variant | LOW | c.1476G>C | p.Val492Val | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 1656/1998 | 1476/1536 | 492/511 | chr11 | 66843174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:66744819 | G | GGGC | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(3): Show |
80 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(77): Show |
5_prime_UTR_variant | MODIFIER | c.-106_-104dupCGG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/15 | 14226 | INFO_REALIGN_3_PRIME | chr11 | 66744819 | |||||
| chr11:66744819 | G | GGGCGGC | 2 | a0001c0001t0003 a0001c0001t0012 |
11 | HG00099.hp1 HG01074.hp1 HG01175.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-109_-104dupCGGCGG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/15 | 14226 | INFO_REALIGN_3_PRIME | chr11 | 66744819 | |||||
| chr11:66744819 | G | GGGCGGCG others(5): Show |
1 | a0001c0001t0011 | 1 | HG02071.hp2 | 5_prime_UTR_variant | MODIFIER | c.-115_-104dupCGGCGG others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/15 | 14226 | INFO_REALIGN_3_PRIME | chr11 | 66744819 | |||||
| chr11:66744819 | G | GGGCGGCG others(8): Show |
1 | a0001c0001t0010 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-118_-104dupCGGCGG others(9): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/15 | 14226 | INFO_REALIGN_3_PRIME | chr11 | 66744819 | |||||
| chr11:66843272 | G | T | 1 | a0001c0001t0012 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 38 | chr11 | 66843272 | ||||||
| chr11:66843334 | C | T | 1 | a0001c0002t0013 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 100 | chr11 | 66843334 | ||||||
| chr11:66843352 | G | GGGCCC | 1 | a0001c0001t0007 | 3 | HG01123.hp1 HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*121_*125dupCCCGG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 126 | INFO_REALIGN_3_PRIME | chr11 | 66843352 | |||||
| chr11:66843357 | CGGGCG | C | 5 | a0001c0001t0009 a0002c0003t0005 a0003c0004t0008 others(2): Show |
10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*139_*143delGGGCG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 139 | INFO_REALIGN_3_PRIME | chr11 | 66843357 | |||||
| chr11:66843423 | G | C | 3 | a0001c0001t0009 a0003c0004t0008 a0007c0006t0009 |
4 | HG01109.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*189G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 189 | chr11 | 66843423 | ||||||
| chr11:66843507 | G | C | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(1): Show |
15 | HG01243.hp2 HG01934.hp1 HG02109.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*273G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 15/15 | 273 | chr11 | 66843507 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:66744924 | T | C | 2 | a0001c0001t0003g0001 a0001c0001t0003g0002 |
2 | HG01515.hp2 HG03942.hp1 |
splice_region_variant&intron_variant | LOW | c.-30+5T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66744924 | |||||||
| chr11:66744967 | G | GGGCTTTG others(10): Show |
1 | a0001c0001t0002g0248 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-30+50_-30+66dupGC others(15): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66744967 | ||||||
| chr11:66745057 | C | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+138C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745057 | |||||||
| chr11:66745180 | G | A | 1 | a0001c0002t0001g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-30+261G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745180 | |||||||
| chr11:66745191 | G | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+272G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745191 | |||||||
| chr11:66745309 | C | CG | 40 | a0001c0001t0001g0197 a0001c0001t0001g0199 a0001c0001t0001g0200 others(37): Show |
40 | HG00438.hp1 HG00609.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.-30+394dupG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745309 | ||||||
| chr11:66745309 | C | CGG | 10 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(7): Show |
10 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30+393_-30+394dup others(2): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745309 | ||||||
| chr11:66745311 | G | C | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-30+392G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745311 | |||||||
| chr11:66745311 | G | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-30+392G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745311 | |||||||
| chr11:66745312 | G | T | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-30+393G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745312 | |||||||
| chr11:66745314 | T | G | 242 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-30+395T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745314 | |||||||
| chr11:66745793 | G | GGTTT | 41 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(38): Show |
41 | HG00323.hp1 HG00621.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.-30+903_-30+906dup others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745793 | ||||||
| chr11:66745793 | G | GGTTTGTT others(1): Show |
3 | a0001c0001t0001g0239 a0001c0001t0004g0240 a0001c0002t0001g0007 |
3 | HG02109.hp1 HG02922.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-30+899_-30+906dup others(8): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745793 | ||||||
| chr11:66745793 | G | GGTTTGTT others(5): Show |
1 | a0001c0001t0002g0006 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-30+895_-30+906dup others(12): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745793 | ||||||
| chr11:66745793 | G | GGTTTGTT others(9): Show |
1 | a0001c0001t0002g0005 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-30+891_-30+906dup others(16): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745793 | ||||||
| chr11:66745793 | GGTTT | G | 91 | a0001c0001t0001g0125 a0001c0001t0001g0131 a0001c0001t0001g0138 others(88): Show |
91 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-30+903_-30+906del others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745793 | ||||||
| chr11:66745793 | GGTTTGTT others(5): Show |
G | 1 | a0001c0001t0002g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-30+895_-30+906del others(12): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66745793 | ||||||
| chr11:66745940 | A | G | 1 | a0001c0001t0004g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-30+1021A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66745940 | |||||||
| chr11:66746263 | C | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+1344C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66746263 | |||||||
| chr11:66746302 | G | T | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | NA18941.hp1 NA18942.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+1383G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66746302 | |||||||
| chr11:66746498 | T | G | 2 | a0001c0001t0002g0122 a0001c0001t0002g0248 |
2 | NA18998.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-30+1579T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66746498 | |||||||
| chr11:66746594 | A | G | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-30+1675A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66746594 | |||||||
| chr11:66746714 | C | CA | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+1807dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66746714 | ||||||
| chr11:66746754 | C | A | 7 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+1835C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66746754 | |||||||
| chr11:66746882 | T | G | 1 | a0001c0001t0001g0041 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-30+1963T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66746882 | |||||||
| chr11:66747189 | A | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-30+2270A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747189 | |||||||
| chr11:66747196 | G | A | 2 | a0001c0001t0002g0123 a0001c0001t0002g0124 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-30+2277G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747196 | |||||||
| chr11:66747394 | AT | A | 5 | a0001c0001t0003g0001 a0002c0003t0005g0118 a0002c0003t0005g0237 others(2): Show |
5 | HG01515.hp2 HG01884.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+2490delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66747394 | ||||||
| chr11:66747427 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0002g0190 |
2 | HG02165.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-30+2508A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747427 | |||||||
| chr11:66747445 | A | C | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-30+2526A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747445 | |||||||
| chr11:66747525 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-30+2606T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747525 | |||||||
| chr11:66747527 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-30+2608T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747527 | |||||||
| chr11:66747644 | A | C | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-30+2725A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747644 | |||||||
| chr11:66747864 | C | T | 10 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(7): Show |
10 | HG00280.hp2 HG01074.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30+2945C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747864 | |||||||
| chr11:66747909 | C | T | 2 | a0001c0001t0004g0184 a0001c0001t0004g0185 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-30+2990C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747909 | |||||||
| chr11:66747911 | C | T | 1 | a0001c0002t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-30+2992C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66747911 | |||||||
| chr11:66748015 | T | C | 1 | a0001c0001t0002g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-30+3096T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66748015 | |||||||
| chr11:66748578 | T | C | 26 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(23): Show |
26 | HG00280.hp1 HG00609.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-30+3659T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66748578 | |||||||
| chr11:66748628 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-30+3709A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66748628 | |||||||
| chr11:66748681 | A | T | 1 | a0001c0001t0001g0246 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-30+3762A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66748681 | |||||||
| chr11:66748871 | C | CA | 14 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(11): Show |
14 | HG00423.hp1 HG01109.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-30+3970dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66748871 | ||||||
| chr11:66749048 | TTG | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+4144_-30+4145d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66749048 | ||||||
| chr11:66749078 | T | A | 1 | a0001c0001t0002g0127 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-30+4159T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749078 | |||||||
| chr11:66749293 | T | A | 1 | a0001c0001t0002g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-30+4374T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749293 | |||||||
| chr11:66749367 | G | A | 1 | a0002c0003t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-30+4448G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749367 | |||||||
| chr11:66749408 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-30+4489A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749408 | |||||||
| chr11:66749491 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-30+4572A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749491 | |||||||
| chr11:66749534 | T | C | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-30+4615T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749534 | |||||||
| chr11:66749616 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-30+4697C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749616 | |||||||
| chr11:66749858 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+4939G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66749858 | |||||||
| chr11:66750013 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+5094A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66750013 | |||||||
| chr11:66750075 | A | G | 7 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0107 others(4): Show |
7 | HG00438.hp2 HG02165.hp1 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+5156A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66750075 | |||||||
| chr11:66750197 | A | AT | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+5286dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66750197 | ||||||
| chr11:66750215 | T | A | 2 | a0001c0002t0001g0064 a0001c0002t0002g0065 |
2 | HG02055.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-30+5296T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66750215 | |||||||
| chr11:66750511 | G | A | 1 | a0001c0002t0001g0009 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-30+5592G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66750511 | |||||||
| chr11:66750528 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+5609A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66750528 | |||||||
| chr11:66750703 | C | CT | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
13 | HG00438.hp2 HG00621.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30+5794dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66750703 | ||||||
| chr11:66750789 | G | T | 1 | a0001c0002t0001g0033 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-30+5870G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66750789 | |||||||
| chr11:66751252 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-30+6333C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751252 | |||||||
| chr11:66751418 | C | T | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | NA18943.hp2 NA18990.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30+6499C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751418 | |||||||
| chr11:66751468 | T | C | 7 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+6549T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751468 | |||||||
| chr11:66751498 | A | AT | 33 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(30): Show |
33 | HG00408.hp1 HG00423.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.-30+6598dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66751498 | ||||||
| chr11:66751498 | A | ATT | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30+6597_-30+6598d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66751498 | ||||||
| chr11:66751498 | AT | A | 7 | a0001c0001t0001g0131 a0001c0001t0001g0210 a0001c0001t0001g0231 others(4): Show |
7 | HG02738.hp1 HG02895.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.-30+6598delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66751498 | ||||||
| chr11:66751519 | T | C | 48 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0197 others(45): Show |
48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-30+6600T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751519 | |||||||
| chr11:66751519 | T | G | 1 | a0001c0001t0002g0132 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-30+6600T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751519 | |||||||
| chr11:66751548 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA19009.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.-30+6629G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751548 | |||||||
| chr11:66751888 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0003g0201 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-30+6969C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751888 | |||||||
| chr11:66751985 | C | G | 1 | a0001c0002t0001g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29-7058C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66751985 | |||||||
| chr11:66752019 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-29-7024A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66752019 | |||||||
| chr11:66752142 | C | CT | 8 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0091 others(5): Show |
8 | HG00438.hp1 HG02735.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-6884dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66752142 | ||||||
| chr11:66752142 | CT | C | 13 | a0001c0001t0001g0092 a0001c0001t0001g0199 a0001c0001t0002g0129 others(10): Show |
13 | HG00609.hp2 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-29-6884delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66752142 | ||||||
| chr11:66752144 | T | C | 9 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0204 others(6): Show |
9 | HG00323.hp1 HG01361.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-6899T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66752144 | |||||||
| chr11:66752159 | T | A | 1 | a0001c0001t0006g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-29-6884T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66752159 | |||||||
| chr11:66752544 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-29-6499C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66752544 | |||||||
| chr11:66752749 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-29-6294G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66752749 | |||||||
| chr11:66752992 | G | A | 2 | a0001c0001t0002g0127 a0001c0001t0002g0135 |
2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-29-6051G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66752992 | |||||||
| chr11:66753012 | C | T | 1 | a0001c0002t0001g0026 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-29-6031C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753012 | |||||||
| chr11:66753061 | G | A | 1 | a0001c0002t0001g0066 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-29-5982G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753061 | |||||||
| chr11:66753137 | A | T | 131 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0041 others(128): Show |
131 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.-29-5906A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753137 | |||||||
| chr11:66753406 | C | CT | 5 | a0001c0001t0002g0173 a0001c0001t0002g0174 a0001c0001t0002g0223 others(2): Show |
5 | HG01261.hp2 HG01928.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29-5619dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66753406 | ||||||
| chr11:66753406 | CT | C | 117 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0041 others(114): Show |
117 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.-29-5619delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66753406 | ||||||
| chr11:66753567 | C | T | 24 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(21): Show |
24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.-29-5476C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753567 | |||||||
| chr11:66753607 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-29-5436C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753607 | |||||||
| chr11:66753623 | G | T | 34 | a0001c0001t0001g0078 a0001c0001t0001g0197 a0001c0002t0001g0009 others(31): Show |
34 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.-29-5420G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753623 | |||||||
| chr11:66753924 | C | T | 1 | a0001c0002t0001g0025 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-29-5119C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66753924 | |||||||
| chr11:66754348 | C | G | 2 | a0001c0001t0004g0184 a0001c0001t0004g0185 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-29-4695C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66754348 | |||||||
| chr11:66754432 | C | T | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-29-4611C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66754432 | |||||||
| chr11:66754605 | G | A | 1 | a0001c0002t0001g0067 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-29-4438G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66754605 | |||||||
| chr11:66754797 | C | G | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-29-4246C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66754797 | |||||||
| chr11:66754846 | A | G | 6 | a0001c0001t0002g0171 a0001c0001t0006g0080 a0001c0001t0006g0087 others(3): Show |
6 | HG01934.hp1 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-4197A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66754846 | |||||||
| chr11:66755120 | G | T | 1 | a0001c0001t0002g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-29-3923G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755120 | |||||||
| chr11:66755121 | A | AT | 53 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0078 others(50): Show |
53 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.-29-3906dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66755121 | ||||||
| chr11:66755121 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-3922A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755121 | |||||||
| chr11:66755121 | AT | A | 10 | a0001c0001t0004g0081 a0001c0001t0004g0082 a0001c0001t0004g0121 others(7): Show |
10 | HG01243.hp2 HG01934.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-29-3906delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66755121 | ||||||
| chr11:66755139 | A | G | 1 | a0001c0002t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-29-3904A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755139 | |||||||
| chr11:66755150 | C | T | 4 | a0001c0001t0001g0078 a0001c0002t0001g0031 a0001c0002t0001g0076 others(1): Show |
4 | HG02132.hp2 NA18960.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-29-3893C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755150 | |||||||
| chr11:66755160 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-29-3883C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755160 | |||||||
| chr11:66755341 | G | C | 40 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(37): Show |
40 | HG00408.hp1 HG00423.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.-29-3702G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755341 | |||||||
| chr11:66755870 | T | C | 1 | a0001c0002t0002g0192 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-29-3173T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755870 | |||||||
| chr11:66755904 | A | T | 9 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(6): Show |
9 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-3139A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66755904 | |||||||
| chr11:66756331 | T | C | 3 | a0001c0001t0002g0136 a0004c0005t0005g0119 a0004c0005t0005g0236 |
3 | HG02647.hp1 NA18906.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-29-2712T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66756331 | |||||||
| chr11:66756338 | T | C | 1 | a0001c0001t0003g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-29-2705T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66756338 | |||||||
| chr11:66756649 | T | G | 1 | a0001c0001t0002g0006 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-29-2394T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66756649 | |||||||
| chr11:66756780 | C | T | 1 | a0002c0003t0005g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-29-2263C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66756780 | |||||||
| chr11:66756795 | T | A | 1 | a0001c0001t0002g0175 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-29-2248T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66756795 | |||||||
| chr11:66757033 | C | T | 4 | a0001c0001t0001g0197 a0001c0002t0001g0009 a0001c0002t0001g0025 others(1): Show |
4 | HG01169.hp2 HG01433.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-2010C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757033 | |||||||
| chr11:66757180 | T | A | 1 | a0001c0001t0003g0137 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-29-1863T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757180 | |||||||
| chr11:66757200 | G | A | 1 | a0001c0002t0013g0071 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-29-1843G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757200 | |||||||
| chr11:66757291 | T | C | 244 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(241): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.-29-1752T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757291 | |||||||
| chr11:66757356 | T | C | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-29-1687T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757356 | |||||||
| chr11:66757417 | A | C | 1 | a0006c0009t0001g0008 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-29-1626A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757417 | |||||||
| chr11:66757461 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-29-1582A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757461 | |||||||
| chr11:66757754 | T | G | 2 | a0001c0001t0002g0122 a0001c0001t0002g0248 |
2 | NA18998.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-29-1289T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66757754 | |||||||
| chr11:66758302 | C | CTTTTCTT others(2): Show |
9 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0037 others(6): Show |
9 | HG00438.hp2 HG00621.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-737_-29-736ins others(9): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | ||||||
| chr11:66758302 | C | CTTTTCTT others(3): Show |
4 | a0001c0001t0001g0035 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG02080.hp1 HG02165.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-737_-29-736ins others(10): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | ||||||
| chr11:66758302 | C | CTTTTTTT others(1): Show |
25 | a0001c0001t0001g0012 a0001c0001t0001g0042 a0001c0001t0001g0043 others(22): Show |
25 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.-29-721_-29-714dup others(8): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | ||||||
| chr11:66758302 | C | CTTTTTTT others(2): Show |
28 | a0001c0001t0001g0029 a0001c0001t0001g0046 a0001c0001t0001g0047 others(25): Show |
28 | HG00099.hp2 HG00323.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.-29-722_-29-714dup others(9): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | ||||||
| chr11:66758302 | C | CTTTTTTT others(3): Show |
13 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(10): Show |
13 | HG01123.hp2 HG01169.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-29-723_-29-714dup others(10): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | ||||||
| chr11:66758302 | C | CTTTTTTT others(4): Show |
8 | a0001c0001t0001g0041 a0001c0001t0001g0052 a0001c0001t0001g0232 others(5): Show |
8 | HG00621.hp1 HG00738.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29-724_-29-714dup others(11): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | ||||||
| chr11:66758302 | C | CTTTTTTT others(5): Show |
9 | a0001c0001t0001g0078 a0001c0001t0001g0204 a0001c0001t0001g0231 others(6): Show |
9 | HG01109.hp1 HG01361.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-725_-29-714dup others(12): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | ||||||
| chr11:66758302 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0003g0243 a0001c0002t0001g0079 |
2 | HG03486.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-29-726_-29-714dup others(13): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | ||||||
| chr11:66758302 | CT | C | 33 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(30): Show |
33 | HG00408.hp1 HG00423.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.-29-714delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | ||||||
| chr11:66758302 | CTTTTT | C | 18 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0163 others(15): Show |
18 | HG00738.hp2 HG02109.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.-29-718_-29-714del others(5): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | ||||||
| chr11:66758302 | CTTTTTT | C | 66 | a0001c0001t0001g0131 a0001c0001t0001g0140 a0001c0001t0001g0149 others(63): Show |
66 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.-29-719_-29-714del others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | ||||||
| chr11:66758302 | CTTTTTTT | C | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0002g0127 others(2): Show |
5 | HG01433.hp1 HG02895.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29-720_-29-714del others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr11 | 66758302 | ||||||
| chr11:66758304 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-29-739T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758304 | |||||||
| chr11:66758334 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0051 a0001c0001t0001g0091 others(4): Show |
7 | NA18946.hp2 NA18955.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.-29-709C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758334 | |||||||
| chr11:66758420 | C | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-623C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758420 | |||||||
| chr11:66758532 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0002g0141 |
3 | HG00609.hp1 NA18960.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-29-511T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758532 | |||||||
| chr11:66758588 | G | A | 242 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-29-455G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758588 | |||||||
| chr11:66758593 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-29-450C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758593 | |||||||
| chr11:66758834 | C | T | 10 | a0001c0001t0009g0004 a0002c0003t0005g0118 a0002c0003t0005g0120 others(7): Show |
10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-29-209C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758834 | |||||||
| chr11:66758861 | T | C | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29-182T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 1/14 | chr11 | 66758861 | |||||||
| chr11:66759108 | C | T | 1 | a0001c0001t0003g0001 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.25+12C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66759108 | |||||||
| chr11:66759646 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.25+550C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66759646 | |||||||
| chr11:66759792 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.25+696A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66759792 | |||||||
| chr11:66760176 | CCAGTGGC others(322): Show |
C | 6 | a0001c0001t0001g0204 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+1112_25+1440del | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760176 | ||||||
| chr11:66760307 | G | A | 1 | a0001c0002t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.25+1211G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66760307 | |||||||
| chr11:66760578 | T | G | 2 | a0001c0001t0001g0056 a0001c0001t0003g0201 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.25+1482T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66760578 | |||||||
| chr11:66760625 | C | CA | 81 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0057 others(78): Show |
81 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.25+1558dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760625 | ||||||
| chr11:66760625 | C | CAA | 20 | a0001c0001t0001g0094 a0001c0001t0001g0189 a0001c0001t0002g0122 others(17): Show |
20 | HG00642.hp2 HG00738.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.25+1557_25+1558dup others(2): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760625 | ||||||
| chr11:66760625 | CA | C | 8 | a0001c0001t0001g0104 a0001c0001t0001g0111 a0001c0001t0001g0112 others(5): Show |
8 | HG00280.hp2 HG00323.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.25+1558delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760625 | ||||||
| chr11:66760625 | CAAAAAA | C | 6 | a0001c0001t0001g0042 a0001c0001t0001g0053 a0001c0001t0001g0054 others(3): Show |
6 | HG02683.hp2 HG03669.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+1553_25+1558del others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760625 | ||||||
| chr11:66760625 | CAAAAAAA | C | 20 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0046 others(17): Show |
20 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.25+1552_25+1558del others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760625 | ||||||
| chr11:66760835 | A | G | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.25+1739A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66760835 | |||||||
| chr11:66760904 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0230 |
2 | NA18939.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.25+1808C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66760904 | |||||||
| chr11:66760994 | C | CT | 24 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(21): Show |
24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+1913dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760994 | ||||||
| chr11:66760994 | CT | C | 8 | a0001c0001t0001g0104 a0001c0001t0001g0112 a0001c0001t0002g0221 others(5): Show |
8 | HG01934.hp1 HG02965.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.25+1913delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66760994 | ||||||
| chr11:66761112 | C | G | 2 | a0001c0001t0004g0184 a0001c0001t0004g0185 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.25+2016C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761112 | |||||||
| chr11:66761147 | G | A | 9 | a0001c0001t0001g0057 a0001c0001t0001g0092 a0001c0001t0001g0093 others(6): Show |
9 | HG00408.hp1 HG02040.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.25+2051G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761147 | |||||||
| chr11:66761223 | T | C | 48 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0197 others(45): Show |
48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.25+2127T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761223 | |||||||
| chr11:66761319 | C | T | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.25+2223C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761319 | |||||||
| chr11:66761577 | A | C | 2 | a0001c0001t0002g0127 a0001c0001t0002g0135 |
2 | HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.25+2481A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761577 | |||||||
| chr11:66761646 | G | T | 10 | a0001c0001t0009g0004 a0002c0003t0005g0118 a0002c0003t0005g0120 others(7): Show |
10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.25+2550G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761646 | |||||||
| chr11:66761650 | C | A | 1 | a0001c0001t0003g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.25+2554C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761650 | |||||||
| chr11:66761692 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.25+2596C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66761692 | |||||||
| chr11:66762246 | A | G | 7 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+3150A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762246 | |||||||
| chr11:66762292 | G | A | 27 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(24): Show |
27 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.25+3196G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762292 | |||||||
| chr11:66762299 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0052 |
2 | HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.25+3203C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762299 | |||||||
| chr11:66762364 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.25+3268C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762364 | |||||||
| chr11:66762368 | A | G | 3 | a0001c0001t0001g0204 a0001c0001t0001g0234 a0001c0001t0003g0002 |
3 | HG02602.hp1 HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.25+3272A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762368 | |||||||
| chr11:66762370 | A | G | 1 | a0001c0001t0002g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.25+3274A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762370 | |||||||
| chr11:66762425 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.25+3329G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762425 | |||||||
| chr11:66762458 | G | A | 1 | a0002c0003t0005g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.25+3362G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762458 | |||||||
| chr11:66762492 | C | T | 1 | a0001c0001t0002g0159 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.25+3396C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762492 | |||||||
| chr11:66762500 | C | T | 27 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(24): Show |
27 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.25+3404C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762500 | |||||||
| chr11:66762637 | T | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+3541T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66762637 | |||||||
| chr11:66763002 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.25+3906A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66763002 | |||||||
| chr11:66763034 | C | T | 2 | a0001c0001t0002g0123 a0001c0001t0002g0124 |
2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.25+3938C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66763034 | |||||||
| chr11:66763219 | A | G | 32 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(29): Show |
32 | HG00280.hp1 HG00609.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.25+4123A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66763219 | |||||||
| chr11:66764213 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.25+5117C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764213 | |||||||
| chr11:66764254 | T | A | 1 | a0001c0001t0002g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.25+5158T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764254 | |||||||
| chr11:66764326 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.25+5230T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764326 | |||||||
| chr11:66764456 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.25+5360G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764456 | |||||||
| chr11:66764496 | C | CA | 19 | a0001c0001t0001g0043 a0001c0001t0001g0113 a0001c0001t0001g0115 others(16): Show |
19 | HG00738.hp2 HG01243.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.25+5419dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66764496 | ||||||
| chr11:66764496 | C | CAA | 5 | a0001c0001t0004g0185 a0002c0003t0005g0118 a0002c0003t0005g0120 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.25+5418_25+5419dup others(2): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66764496 | ||||||
| chr11:66764568 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.25+5472G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764568 | |||||||
| chr11:66764580 | G | A | 1 | a0001c0002t0001g0193 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.25+5484G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764580 | |||||||
| chr11:66764619 | C | T | 1 | a0001c0002t0001g0021 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.25+5523C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764619 | |||||||
| chr11:66764643 | C | T | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.25+5547C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764643 | |||||||
| chr11:66764665 | C | CA | 46 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0197 others(43): Show |
46 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.25+5583dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66764665 | ||||||
| chr11:66764680 | TAAA | T | 26 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(23): Show |
26 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.25+5585_25+5587del others(3): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764680 | |||||||
| chr11:66764681 | A | G | 2 | a0001c0001t0002g0132 a0001c0001t0002g0225 |
2 | HG00438.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.25+5585A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764681 | |||||||
| chr11:66764683 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.25+5587A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764683 | |||||||
| chr11:66764761 | C | T | 2 | a0001c0001t0001g0239 a0001c0001t0004g0240 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.25+5665C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764761 | |||||||
| chr11:66764838 | G | C | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.25+5742G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764838 | |||||||
| chr11:66764968 | CA | C | 6 | a0001c0001t0001g0204 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+5883delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66764968 | ||||||
| chr11:66764990 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.25+5894T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764990 | |||||||
| chr11:66764994 | G | A | 8 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0095 others(5): Show |
8 | HG00423.hp1 HG02040.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.25+5898G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66764994 | |||||||
| chr11:66765109 | A | G | 1 | a0001c0001t0002g0174 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.25+6013A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66765109 | |||||||
| chr11:66765143 | G | A | 1 | a0001c0002t0001g0023 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.25+6047G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66765143 | |||||||
| chr11:66765148 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.25+6052A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66765148 | |||||||
| chr11:66765499 | G | A | 26 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(23): Show |
26 | HG00280.hp1 HG00609.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.25+6403G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66765499 | |||||||
| chr11:66765998 | C | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+6902C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66765998 | |||||||
| chr11:66766347 | T | G | 7 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+7251T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66766347 | |||||||
| chr11:66766442 | C | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+7346C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66766442 | |||||||
| chr11:66766522 | G | C | 1 | a0001c0001t0002g0159 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.25+7426G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66766522 | |||||||
| chr11:66766535 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0003g0201 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.25+7439C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66766535 | |||||||
| chr11:66766766 | A | T | 5 | a0001c0001t0006g0080 a0001c0001t0006g0087 a0001c0001t0006g0089 others(2): Show |
5 | HG01934.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+7670A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66766766 | |||||||
| chr11:66767045 | T | C | 48 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0197 others(45): Show |
48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.25+7949T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767045 | |||||||
| chr11:66767046 | T | C | 24 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(21): Show |
24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+7950T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767046 | |||||||
| chr11:66767084 | C | T | 3 | a0002c0003t0005g0237 a0004c0005t0005g0119 a0004c0005t0005g0236 |
3 | HG02615.hp2 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.25+7988C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767084 | |||||||
| chr11:66767097 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.25+8001A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767097 | |||||||
| chr11:66767178 | A | T | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.25+8082A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767178 | |||||||
| chr11:66767343 | T | G | 7 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+8247T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767343 | |||||||
| chr11:66767852 | A | G | 48 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0197 others(45): Show |
48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.25+8756A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767852 | |||||||
| chr11:66767953 | A | T | 24 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(21): Show |
24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+8857A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66767953 | |||||||
| chr11:66768603 | G | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.25+9507G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66768603 | |||||||
| chr11:66768668 | G | GT | 5 | a0001c0001t0001g0053 a0001c0001t0001g0117 a0001c0001t0002g0151 others(2): Show |
5 | NA18949.hp1 NA19068.hp2 NA19082.hp2 others(2): Show |
intron_variant | MODIFIER | c.25+9587dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66768668 | ||||||
| chr11:66768668 | GT | G | 12 | a0001c0001t0001g0113 a0001c0001t0006g0080 a0001c0001t0006g0087 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.25+9587delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66768668 | ||||||
| chr11:66768675 | T | G | 3 | a0001c0001t0007g0226 a0001c0001t0007g0227 a0001c0001t0007g0228 |
3 | HG01123.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.25+9579T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66768675 | |||||||
| chr11:66768983 | G | A | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.25+9887G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66768983 | |||||||
| chr11:66769042 | G | C | 6 | a0001c0001t0001g0204 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.25+9946G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769042 | |||||||
| chr11:66769175 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.25+10079A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769175 | |||||||
| chr11:66769318 | A | G | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.25+10222A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769318 | |||||||
| chr11:66769343 | A | T | 1 | a0006c0009t0001g0008 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.25+10247A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769343 | |||||||
| chr11:66769354 | C | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+10258C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769354 | |||||||
| chr11:66769355 | G | A | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.25+10259G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769355 | |||||||
| chr11:66769435 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.25+10339G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769435 | |||||||
| chr11:66769448 | T | TA | 7 | a0001c0001t0001g0028 a0001c0002t0001g0064 a0001c0002t0001g0067 others(4): Show |
7 | HG01109.hp2 HG02055.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+10364dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66769448 | ||||||
| chr11:66769639 | T | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0210 |
2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.25+10543T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66769639 | |||||||
| chr11:66770155 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.25+11059G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66770155 | |||||||
| chr11:66770564 | C | A | 24 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(21): Show |
24 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.25+11468C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66770564 | |||||||
| chr11:66770944 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.25+11848G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66770944 | |||||||
| chr11:66770982 | C | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA19009.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.25+11886C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66770982 | |||||||
| chr11:66771112 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0004g0240 |
2 | HG02109.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.25+12016A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66771112 | |||||||
| chr11:66771385 | T | C | 7 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.25+12289T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66771385 | |||||||
| chr11:66771581 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+12485G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66771581 | |||||||
| chr11:66771687 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.25+12591A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66771687 | |||||||
| chr11:66771718 | T | C | 1 | a0001c0002t0001g0075 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.25+12622T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66771718 | |||||||
| chr11:66772192 | T | A | 1 | a0001c0001t0002g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.25+13096T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66772192 | |||||||
| chr11:66772370 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.25+13274C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66772370 | |||||||
| chr11:66772385 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.25+13289T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66772385 | |||||||
| chr11:66772914 | A | G | 1 | a0001c0001t0004g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.25+13818A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66772914 | |||||||
| chr11:66773054 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.25+13958C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66773054 | |||||||
| chr11:66773483 | C | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.25+14387C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66773483 | |||||||
| chr11:66773767 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.26-14393C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66773767 | |||||||
| chr11:66774539 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.26-13621C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66774539 | |||||||
| chr11:66774589 | G | A | 1 | a0001c0002t0001g0010 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.26-13571G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66774589 | |||||||
| chr11:66774714 | G | A | 1 | a0001c0002t0002g0011 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.26-13446G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66774714 | |||||||
| chr11:66774763 | G | A | 1 | a0002c0003t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-13397G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66774763 | |||||||
| chr11:66774794 | T | A | 1 | a0001c0001t0001g0037 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.26-13366T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66774794 | |||||||
| chr11:66775112 | C | CA | 97 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0049 others(94): Show |
97 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.26-13025dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66775112 | ||||||
| chr11:66775112 | C | CAAA | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-13027_26-13025d others(5): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66775112 | ||||||
| chr11:66775113 | A | C | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-13047A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775113 | |||||||
| chr11:66775242 | C | G | 1 | a0001c0002t0001g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.26-12918C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775242 | |||||||
| chr11:66775335 | C | T | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.26-12825C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775335 | |||||||
| chr11:66775338 | G | A | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.26-12822G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775338 | |||||||
| chr11:66775459 | A | G | 10 | a0001c0001t0001g0078 a0001c0002t0001g0020 a0001c0002t0001g0031 others(7): Show |
10 | HG00621.hp1 HG02132.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.26-12701A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775459 | |||||||
| chr11:66775767 | A | G | 226 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0041 others(223): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.26-12393A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775767 | |||||||
| chr11:66775867 | T | C | 1 | a0001c0002t0002g0011 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.26-12293T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775867 | |||||||
| chr11:66775920 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.26-12240T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66775920 | |||||||
| chr11:66776119 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.26-12041C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776119 | |||||||
| chr11:66776151 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.26-12009C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776151 | |||||||
| chr11:66776229 | G | A | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.26-11931G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776229 | |||||||
| chr11:66776260 | T | C | 1 | a0001c0001t0002g0222 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.26-11900T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776260 | |||||||
| chr11:66776442 | A | G | 3 | a0001c0001t0004g0081 a0001c0001t0004g0082 a0001c0001t0004g0121 |
3 | HG01243.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.26-11718A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776442 | |||||||
| chr11:66776501 | C | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-11659C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776501 | |||||||
| chr11:66776504 | C | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-11656C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776504 | |||||||
| chr11:66776588 | G | A | 6 | a0001c0001t0001g0204 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.26-11572G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776588 | |||||||
| chr11:66776603 | C | G | 1 | a0002c0003t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-11557C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776603 | |||||||
| chr11:66776634 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.26-11526A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776634 | |||||||
| chr11:66776836 | C | G | 11 | a0001c0001t0001g0131 a0001c0001t0001g0139 a0001c0001t0001g0149 others(8): Show |
11 | HG00423.hp2 HG02523.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-11324C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776836 | |||||||
| chr11:66776898 | A | C | 2 | a0001c0001t0001g0056 a0001c0001t0003g0201 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.26-11262A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66776898 | |||||||
| chr11:66777010 | G | A | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG00280.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.26-11150G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777010 | |||||||
| chr11:66777033 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-11127G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777033 | |||||||
| chr11:66777042 | ACTATATC others(7): Show |
A | 1 | a0001c0002t0001g0026 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.26-11089_26-11076d others(16): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66777042 | ||||||
| chr11:66777043 | C | CTATATCT others(31): Show |
7 | a0001c0001t0001g0204 a0001c0001t0001g0231 a0001c0001t0001g0232 others(4): Show |
7 | HG00738.hp2 HG01361.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-11077_26-11040d others(40): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66777043 | ||||||
| chr11:66777057 | CTATATCT others(17): Show |
C | 1 | a0001c0002t0013g0071 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.26-11075_26-11052d others(26): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66777057 | ||||||
| chr11:66777074 | T | G | 3 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0238 |
3 | HG01243.hp1 HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.26-11086T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777074 | |||||||
| chr11:66777081 | ATATATCT others(7): Show |
A | 1 | a0001c0001t0002g0133 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.26-11053_26-11040d others(16): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66777081 | ||||||
| chr11:66777136 | A | G | 1 | a0002c0003t0005g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.26-11024A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777136 | |||||||
| chr11:66777188 | A | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-10972A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777188 | |||||||
| chr11:66777265 | T | G | 1 | a0001c0001t0002g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.26-10895T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777265 | |||||||
| chr11:66777367 | C | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-10793C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777367 | |||||||
| chr11:66777832 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0210 |
3 | HG02630.hp2 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.26-10328A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66777832 | |||||||
| chr11:66778093 | CT | C | 5 | a0001c0001t0001g0106 a0001c0001t0002g0133 a0001c0001t0003g0201 others(2): Show |
5 | HG00099.hp2 HG01168.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.26-10052delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66778093 | ||||||
| chr11:66778243 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.26-9917G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66778243 | |||||||
| chr11:66778860 | A | T | 1 | a0001c0001t0002g0128 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.26-9300A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66778860 | |||||||
| chr11:66779324 | A | G | 1 | a0002c0003t0005g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.26-8836A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779324 | |||||||
| chr11:66779343 | G | A | 1 | a0001c0001t0002g0214 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.26-8817G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779343 | |||||||
| chr11:66779351 | A | G | 2 | a0001c0001t0007g0226 a0001c0001t0007g0228 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.26-8809A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779351 | |||||||
| chr11:66779403 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-8757G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779403 | |||||||
| chr11:66779465 | C | T | 3 | a0001c0002t0001g0067 a0001c0002t0001g0069 a0001c0002t0001g0203 |
3 | NA19030.hp1 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.26-8695C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779465 | |||||||
| chr11:66779635 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.26-8525C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779635 | |||||||
| chr11:66779665 | T | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-8495T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779665 | |||||||
| chr11:66779852 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.26-8308C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779852 | |||||||
| chr11:66779895 | C | G | 1 | a0001c0001t0002g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.26-8265C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66779895 | |||||||
| chr11:66779911 | C | CA | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-8243dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66779911 | ||||||
| chr11:66780015 | T | TG | 19 | a0001c0001t0001g0052 a0001c0001t0001g0125 a0001c0001t0001g0204 others(16): Show |
19 | HG00280.hp2 HG00408.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.26-8139dupG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66780015 | ||||||
| chr11:66780016 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.26-8144G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66780016 | |||||||
| chr11:66780050 | C | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-8110C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66780050 | |||||||
| chr11:66780106 | A | G | 1 | a0001c0001t0001g0039 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.26-8054A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66780106 | |||||||
| chr11:66780151 | C | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-8009C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66780151 | |||||||
| chr11:66780789 | C | G | 32 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(29): Show |
32 | HG00280.hp1 HG00609.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.26-7371C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66780789 | |||||||
| chr11:66780991 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0055 |
3 | HG01928.hp1 NA18994.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.26-7169T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66780991 | |||||||
| chr11:66781104 | A | G | 26 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(23): Show |
26 | HG00280.hp1 HG00609.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.26-7056A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781104 | |||||||
| chr11:66781299 | A | G | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.26-6861A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781299 | |||||||
| chr11:66781343 | T | C | 2 | a0001c0002t0001g0003 a0001c0002t0001g0015 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.26-6817T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781343 | |||||||
| chr11:66781425 | G | A | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.26-6735G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781425 | |||||||
| chr11:66781435 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | NA18950.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.26-6725A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781435 | |||||||
| chr11:66781569 | C | T | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.26-6591C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781569 | |||||||
| chr11:66781698 | C | T | 3 | a0001c0002t0001g0203 a0003c0004t0008g0062 a0003c0004t0008g0063 |
3 | HG01109.hp2 HG03098.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.26-6462C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781698 | |||||||
| chr11:66781846 | A | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-6314A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781846 | |||||||
| chr11:66781947 | A | G | 2 | a0001c0001t0002g0191 a0001c0001t0002g0221 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.26-6213A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66781947 | |||||||
| chr11:66782073 | A | G | 1 | a0001c0002t0001g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.26-6087A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782073 | |||||||
| chr11:66782269 | C | G | 48 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0197 others(45): Show |
48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.26-5891C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782269 | |||||||
| chr11:66782445 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-5715G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782445 | |||||||
| chr11:66782452 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.26-5708G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782452 | |||||||
| chr11:66782500 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0229 |
2 | HG00280.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.26-5660C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782500 | |||||||
| chr11:66782608 | C | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.26-5552C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782608 | |||||||
| chr11:66782980 | G | A | 26 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(23): Show |
26 | HG00280.hp1 HG00609.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.26-5180G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66782980 | |||||||
| chr11:66783073 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.26-5087A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783073 | |||||||
| chr11:66783129 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0186 a0001c0001t0001g0229 |
3 | HG00280.hp2 HG01074.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.26-5031C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783129 | |||||||
| chr11:66783130 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0140 |
2 | NA18960.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.26-5030G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783130 | |||||||
| chr11:66783531 | G | C | 47 | a0001c0001t0001g0078 a0001c0001t0001g0197 a0001c0002t0001g0003 others(44): Show |
47 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.26-4629G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783531 | |||||||
| chr11:66783611 | G | T | 1 | a0001c0001t0002g0133 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.26-4549G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783611 | |||||||
| chr11:66783612 | C | G | 1 | a0001c0001t0002g0133 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.26-4548C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783612 | |||||||
| chr11:66783645 | T | G | 32 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(29): Show |
32 | HG00280.hp1 HG00609.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.26-4515T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783645 | |||||||
| chr11:66783672 | C | T | 100 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0057 others(97): Show |
100 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.26-4488C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783672 | |||||||
| chr11:66783796 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.26-4364A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783796 | |||||||
| chr11:66783879 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-4281G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783879 | |||||||
| chr11:66783977 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.26-4183C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66783977 | |||||||
| chr11:66784017 | TTTTTG | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-4123_26-4119del others(5): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66784017 | ||||||
| chr11:66784049 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-4111G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784049 | |||||||
| chr11:66784099 | C | T | 1 | a0004c0005t0005g0236 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.26-4061C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784099 | |||||||
| chr11:66784157 | A | T | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.26-4003A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784157 | |||||||
| chr11:66784537 | C | G | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.26-3623C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784537 | |||||||
| chr11:66784669 | G | A | 1 | a0001c0001t0002g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.26-3491G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784669 | |||||||
| chr11:66784884 | A | G | 27 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(24): Show |
27 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.26-3276A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784884 | |||||||
| chr11:66784956 | C | CT | 27 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
27 | HG00438.hp2 HG00621.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.26-3183dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66784956 | ||||||
| chr11:66784956 | CT | C | 126 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0041 others(123): Show |
126 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.26-3183delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66784956 | ||||||
| chr11:66784994 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-3166C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66784994 | |||||||
| chr11:66785185 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.26-2975C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785185 | |||||||
| chr11:66785363 | T | G | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.26-2797T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785363 | |||||||
| chr11:66785450 | G | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.26-2710G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785450 | |||||||
| chr11:66785529 | T | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | NA19009.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.26-2631T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785529 | |||||||
| chr11:66785540 | C | A | 4 | a0001c0001t0001g0239 a0001c0001t0001g0242 a0001c0001t0003g0243 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-2620C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785540 | |||||||
| chr11:66785617 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.26-2543A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785617 | |||||||
| chr11:66785835 | C | T | 3 | a0001c0001t0004g0081 a0001c0001t0004g0082 a0001c0001t0004g0121 |
3 | HG01243.hp2 HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.26-2325C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785835 | |||||||
| chr11:66785981 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.26-2179C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66785981 | |||||||
| chr11:66786266 | G | C | 163 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(160): Show |
163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.26-1894G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66786266 | |||||||
| chr11:66786297 | T | TA | 8 | a0001c0001t0001g0149 a0001c0001t0001g0163 a0001c0001t0003g0212 others(5): Show |
8 | HG00423.hp2 HG01175.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.26-1848dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66786297 | ||||||
| chr11:66786297 | TA | T | 11 | a0001c0001t0002g0217 a0001c0001t0004g0081 a0001c0001t0004g0082 others(8): Show |
11 | HG01243.hp2 HG01255.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-1848delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66786297 | ||||||
| chr11:66786313 | T | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0058 a0001c0001t0002g0224 others(1): Show |
4 | HG01261.hp2 HG02080.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-1847T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66786313 | |||||||
| chr11:66786318 | G | A | 2 | a0001c0001t0002g0133 a0001c0001t0002g0157 |
2 | NA18953.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.26-1842G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66786318 | |||||||
| chr11:66786937 | G | GT | 51 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0078 others(48): Show |
51 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.26-1210dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66786937 | ||||||
| chr11:66786937 | G | GTT | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02074.hp2 HG02132.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.26-1211_26-1210dup others(2): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66786937 | ||||||
| chr11:66786937 | G | T | 1 | a0001c0002t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.26-1223G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66786937 | |||||||
| chr11:66786956 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.26-1204G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66786956 | |||||||
| chr11:66787213 | C | T | 1 | a0001c0002t0001g0194 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.26-947C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787213 | |||||||
| chr11:66787431 | C | T | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | NA18941.hp1 NA18942.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.26-729C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787431 | |||||||
| chr11:66787454 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.26-706C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787454 | |||||||
| chr11:66787551 | C | CA | 11 | a0001c0001t0001g0242 a0001c0001t0002g0132 a0001c0001t0002g0177 others(8): Show |
11 | HG01934.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.26-592dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66787551 | ||||||
| chr11:66787551 | CA | C | 117 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0041 others(114): Show |
117 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.26-592delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66787551 | ||||||
| chr11:66787568 | A | G | 1 | a0001c0001t0002g0151 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.26-592A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787568 | |||||||
| chr11:66787593 | G | A | 1 | a0001c0002t0001g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.26-567G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787593 | |||||||
| chr11:66787676 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.26-484C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787676 | |||||||
| chr11:66787715 | G | A | 1 | a0001c0002t0001g0202 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.26-445G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787715 | |||||||
| chr11:66787719 | C | CA | 12 | a0001c0001t0001g0083 a0001c0001t0001g0096 a0001c0001t0002g0132 others(9): Show |
12 | HG00438.hp1 HG01175.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.26-426dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr11 | 66787719 | ||||||
| chr11:66787971 | A | G | 1 | a0002c0003t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.26-189A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66787971 | |||||||
| chr11:66788001 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.26-159G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66788001 | |||||||
| chr11:66788024 | C | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.26-136C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 2/14 | chr11 | 66788024 | |||||||
| chr11:66788404 | GC | G | 6 | a0001c0001t0001g0204 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+137delC | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66788404 | ||||||
| chr11:66788405 | C | G | 1 | a0001c0001t0002g0006 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.135+136C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66788405 | |||||||
| chr11:66788428 | A | G | 1 | a0001c0001t0002g0220 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.135+159A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66788428 | |||||||
| chr11:66788471 | T | C | 1 | a0002c0003t0005g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.135+202T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66788471 | |||||||
| chr11:66788489 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0117 |
2 | NA18941.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.135+220G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66788489 | |||||||
| chr11:66788596 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.135+327C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66788596 | |||||||
| chr11:66789084 | C | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+815C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66789084 | |||||||
| chr11:66789297 | A | G | 1 | a0005c0008t0002g0165 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.135+1028A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66789297 | |||||||
| chr11:66789369 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.135+1100C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66789369 | |||||||
| chr11:66789715 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.135+1446T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66789715 | |||||||
| chr11:66790005 | G | A | 1 | a0001c0002t0001g0067 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.135+1736G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66790005 | |||||||
| chr11:66790283 | T | C | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.135+2014T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66790283 | |||||||
| chr11:66790644 | G | A | 1 | a0001c0001t0002g0248 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.135+2375G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66790644 | |||||||
| chr11:66790962 | G | A | 3 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 |
3 | HG02723.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.135+2693G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66790962 | |||||||
| chr11:66791271 | T | C | 1 | a0001c0001t0012g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.135+3002T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66791271 | |||||||
| chr11:66791327 | T | C | 10 | a0001c0001t0009g0004 a0002c0003t0005g0118 a0002c0003t0005g0120 others(7): Show |
10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.135+3058T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66791327 | |||||||
| chr11:66791421 | TTATACA | T | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.135+3157_135+3162d others(8): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66791421 | ||||||
| chr11:66791561 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.135+3292A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66791561 | |||||||
| chr11:66791818 | A | AT | 8 | a0001c0001t0001g0034 a0001c0001t0001g0106 a0001c0001t0001g0117 others(5): Show |
8 | HG01109.hp1 HG02602.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+3566dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66791818 | ||||||
| chr11:66792008 | G | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.135+3739G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66792008 | |||||||
| chr11:66792089 | C | T | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.135+3820C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66792089 | |||||||
| chr11:66792114 | C | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.135+3845C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66792114 | |||||||
| chr11:66792242 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.135+3973C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66792242 | |||||||
| chr11:66792552 | A | G | 47 | a0001c0001t0001g0078 a0001c0001t0001g0197 a0001c0002t0001g0003 others(44): Show |
47 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.136-3729A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66792552 | |||||||
| chr11:66792792 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.136-3489G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66792792 | |||||||
| chr11:66793072 | C | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0137 |
2 | HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.136-3209C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793072 | |||||||
| chr11:66793092 | GT | G | 48 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0197 others(45): Show |
48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.136-3176delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66793092 | ||||||
| chr11:66793133 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-3148G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793133 | |||||||
| chr11:66793253 | AT | A | 30 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(27): Show |
30 | HG00280.hp2 HG00438.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.136-3019delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66793253 | ||||||
| chr11:66793262 | T | C | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.136-3019T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793262 | |||||||
| chr11:66793409 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.136-2872T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793409 | |||||||
| chr11:66793444 | G | GT | 55 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0047 others(52): Show |
55 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.136-2817dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66793444 | ||||||
| chr11:66793444 | G | GTT | 6 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0229 others(3): Show |
6 | HG00099.hp1 HG01261.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-2818_136-2817d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66793444 | ||||||
| chr11:66793444 | G | T | 2 | a0001c0001t0002g0156 a0001c0001t0002g0220 |
2 | NA18970.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.136-2837G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793444 | |||||||
| chr11:66793444 | GT | G | 7 | a0001c0001t0009g0004 a0002c0003t0005g0118 a0002c0003t0005g0120 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-2817delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66793444 | ||||||
| chr11:66793447 | T | G | 1 | a0001c0001t0004g0082 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.136-2834T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793447 | |||||||
| chr11:66793449 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.136-2832T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793449 | |||||||
| chr11:66793511 | T | C | 48 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0197 others(45): Show |
48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.136-2770T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793511 | |||||||
| chr11:66793714 | G | T | 1 | a0001c0001t0002g0223 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.136-2567G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793714 | |||||||
| chr11:66793908 | C | G | 1 | a0001c0001t0001g0012 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.136-2373C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66793908 | |||||||
| chr11:66794099 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.136-2182G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66794099 | |||||||
| chr11:66794112 | T | TA | 50 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0197 others(47): Show |
50 | HG00099.hp2 HG00621.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.136-2149dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66794112 | ||||||
| chr11:66794112 | TA | T | 11 | a0001c0001t0001g0083 a0001c0001t0002g0044 a0001c0001t0002g0130 others(8): Show |
11 | HG00280.hp1 HG01109.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-2149delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66794112 | ||||||
| chr11:66794440 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.136-1841C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66794440 | |||||||
| chr11:66794777 | T | C | 163 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(160): Show |
163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.136-1504T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66794777 | |||||||
| chr11:66794851 | G | T | 1 | a0001c0002t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.136-1430G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66794851 | |||||||
| chr11:66794858 | C | T | 11 | a0001c0001t0001g0131 a0001c0001t0001g0139 a0001c0001t0001g0149 others(8): Show |
11 | HG00423.hp2 HG02523.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.136-1423C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66794858 | |||||||
| chr11:66794960 | C | T | 24 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(21): Show |
24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.136-1321C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66794960 | |||||||
| chr11:66795134 | C | CA | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-1138dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66795134 | ||||||
| chr11:66795140 | A | AAT | 5 | a0001c0001t0001g0057 a0001c0001t0001g0093 a0001c0001t0001g0097 others(2): Show |
5 | HG00408.hp1 HG02074.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.136-1140_136-1139i others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr11 | 66795140 | ||||||
| chr11:66795142 | A | T | 41 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.136-1139A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795142 | |||||||
| chr11:66795144 | T | A | 8 | a0001c0001t0001g0047 a0001c0001t0002g0145 a0001c0001t0002g0148 others(5): Show |
8 | HG00408.hp2 HG01109.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.136-1137T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795144 | |||||||
| chr11:66795205 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.136-1076T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795205 | |||||||
| chr11:66795312 | T | G | 3 | a0001c0001t0002g0134 a0001c0001t0002g0167 a0001c0001t0002g0168 |
3 | NA18941.hp2 NA18962.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.136-969T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795312 | |||||||
| chr11:66795362 | C | T | 2 | a0001c0001t0004g0184 a0001c0001t0004g0185 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.136-919C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795362 | |||||||
| chr11:66795490 | T | C | 1 | a0001c0001t0002g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136-791T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795490 | |||||||
| chr11:66795494 | G | T | 1 | a0001c0001t0002g0169 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.136-787G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795494 | |||||||
| chr11:66795591 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.136-690C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795591 | |||||||
| chr11:66795594 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.136-687G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795594 | |||||||
| chr11:66795940 | A | G | 1 | a0001c0001t0007g0227 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.136-341A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795940 | |||||||
| chr11:66795957 | T | G | 1 | a0001c0002t0001g0193 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.136-324T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795957 | |||||||
| chr11:66795961 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.136-320A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66795961 | |||||||
| chr11:66796054 | A | G | 10 | a0001c0001t0009g0004 a0002c0003t0005g0118 a0002c0003t0005g0120 others(7): Show |
10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-227A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66796054 | |||||||
| chr11:66796062 | G | A | 1 | a0001c0002t0002g0011 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.136-219G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66796062 | |||||||
| chr11:66796163 | G | C | 10 | a0001c0001t0004g0081 a0001c0001t0004g0082 a0001c0001t0004g0121 others(7): Show |
10 | HG01243.hp2 HG01934.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.136-118G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66796163 | |||||||
| chr11:66796215 | G | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.136-66G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 3/14 | chr11 | 66796215 | |||||||
| chr11:66796551 | G | A | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.219+187G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796551 | |||||||
| chr11:66796699 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.219+335C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796699 | |||||||
| chr11:66796708 | A | G | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.219+344A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796708 | |||||||
| chr11:66796780 | CT | C | 5 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.219+419delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66796780 | ||||||
| chr11:66796783 | T | G | 1 | a0002c0003t0005g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.219+419T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796783 | |||||||
| chr11:66796785 | G | A | 1 | a0002c0003t0005g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.219+421G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796785 | |||||||
| chr11:66796785 | G | GA | 18 | a0001c0001t0001g0207 a0001c0001t0001g0242 a0001c0001t0001g0244 others(15): Show |
18 | HG00438.hp1 HG01123.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.219+438dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66796785 | ||||||
| chr11:66796804 | ACAACTTT | A | 5 | a0001c0001t0001g0204 a0001c0001t0001g0231 a0001c0001t0001g0232 others(2): Show |
5 | HG01361.hp2 HG02071.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.219+451_219+457del others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66796804 | ||||||
| chr11:66796805 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.219+441C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796805 | |||||||
| chr11:66796860 | G | GT | 24 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0083 others(21): Show |
24 | HG00408.hp1 HG02040.hp2 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.219+509dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66796860 | ||||||
| chr11:66796863 | T | TG | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0100 |
3 | HG00423.hp1 HG02040.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.219+499_219+500ins others(1): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66796863 | |||||||
| chr11:66797125 | T | C | 10 | a0001c0001t0004g0081 a0001c0001t0004g0082 a0001c0001t0004g0121 others(7): Show |
10 | HG01243.hp2 HG01934.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.219+761T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66797125 | |||||||
| chr11:66797789 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0207 |
2 | NA18945.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.219+1425G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66797789 | |||||||
| chr11:66797798 | A | G | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(1): Show |
4 | NA18941.hp1 NA18942.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+1434A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66797798 | |||||||
| chr11:66797808 | A | G | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.219+1444A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66797808 | |||||||
| chr11:66797824 | A | C | 1 | a0001c0001t0002g0124 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.219+1460A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66797824 | |||||||
| chr11:66797942 | A | G | 2 | a0001c0001t0001g0242 a0001c0001t0003g0243 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.219+1578A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66797942 | |||||||
| chr11:66798034 | C | T | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.219+1670C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798034 | |||||||
| chr11:66798105 | A | G | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.219+1741A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798105 | |||||||
| chr11:66798263 | C | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.219+1899C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798263 | |||||||
| chr11:66798304 | A | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02602.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.219+1940A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798304 | |||||||
| chr11:66798374 | C | T | 1 | a0002c0003t0005g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.219+2010C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798374 | |||||||
| chr11:66798513 | T | G | 24 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(21): Show |
24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.220-2128T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798513 | |||||||
| chr11:66798597 | C | CA | 30 | a0001c0001t0001g0047 a0001c0001t0001g0052 a0001c0001t0001g0056 others(27): Show |
30 | HG00280.hp2 HG01109.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.220-2020dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66798597 | ||||||
| chr11:66798597 | CA | C | 28 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0102 others(25): Show |
28 | HG00280.hp1 HG00423.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.220-2020delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66798597 | ||||||
| chr11:66798797 | G | A | 27 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(24): Show |
27 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.220-1844G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798797 | |||||||
| chr11:66798957 | G | A | 24 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(21): Show |
24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.220-1684G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66798957 | |||||||
| chr11:66799035 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0100 |
3 | HG00423.hp1 HG02040.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.220-1606C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66799035 | |||||||
| chr11:66799077 | C | A | 1 | a0001c0002t0001g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.220-1564C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66799077 | |||||||
| chr11:66799094 | C | G | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.220-1547C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66799094 | |||||||
| chr11:66799193 | CA | C | 10 | a0001c0001t0004g0081 a0001c0001t0004g0082 a0001c0001t0004g0121 others(7): Show |
10 | HG01243.hp2 HG01934.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-1446delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66799193 | ||||||
| chr11:66799207 | C | CA | 17 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0094 others(14): Show |
17 | HG00642.hp1 HG01433.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.220-1413dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66799207 | ||||||
| chr11:66799207 | CA | C | 8 | a0001c0001t0001g0037 a0001c0001t0001g0230 a0001c0001t0002g0129 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.220-1413delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66799207 | ||||||
| chr11:66799299 | C | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.220-1342C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66799299 | |||||||
| chr11:66799385 | CA | C | 10 | a0001c0001t0001g0230 a0001c0001t0001g0245 a0001c0001t0007g0228 others(7): Show |
10 | HG01169.hp1 HG01169.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.220-1242delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66799385 | ||||||
| chr11:66799541 | A | G | 3 | a0001c0001t0002g0134 a0001c0001t0002g0167 a0001c0001t0002g0168 |
3 | NA18941.hp2 NA18962.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.220-1100A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66799541 | |||||||
| chr11:66799929 | A | T | 27 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(24): Show |
27 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.220-712A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66799929 | |||||||
| chr11:66800004 | C | T | 1 | a0001c0001t0002g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.220-637C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66800004 | |||||||
| chr11:66800064 | C | CA | 23 | a0001c0001t0001g0041 a0001c0001t0001g0046 a0001c0001t0001g0052 others(20): Show |
23 | HG01175.hp1 HG01243.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.220-562dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr11 | 66800064 | ||||||
| chr11:66800344 | A | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.220-297A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 4/14 | chr11 | 66800344 | |||||||
| chr11:66801367 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.347+265A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66801367 | |||||||
| chr11:66801472 | C | T | 174 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(171): Show |
174 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.347+370C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66801472 | |||||||
| chr11:66801888 | G | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.347+786G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66801888 | |||||||
| chr11:66802014 | T | G | 1 | a0001c0001t0002g0174 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.347+912T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66802014 | |||||||
| chr11:66802038 | G | T | 3 | a0001c0001t0007g0226 a0001c0001t0007g0227 a0001c0001t0007g0228 |
3 | HG01123.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.347+936G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66802038 | |||||||
| chr11:66802076 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.347+974G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66802076 | |||||||
| chr11:66802925 | C | G | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.348-1070C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66802925 | |||||||
| chr11:66803036 | T | C | 24 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(21): Show |
24 | HG00280.hp1 HG00609.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.348-959T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803036 | |||||||
| chr11:66803278 | G | A | 163 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(160): Show |
163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.348-717G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803278 | |||||||
| chr11:66803369 | G | A | 3 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 |
3 | HG02723.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.348-626G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803369 | |||||||
| chr11:66803467 | T | C | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.348-528T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803467 | |||||||
| chr11:66803490 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.348-505G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803490 | |||||||
| chr11:66803515 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348-480G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803515 | |||||||
| chr11:66803867 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.348-128A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803867 | |||||||
| chr11:66803971 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.348-24T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 6/14 | chr11 | 66803971 | |||||||
| chr11:66804408 | T | C | 1 | a0001c0001t0002g0160 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.543+218T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66804408 | |||||||
| chr11:66804704 | G | A | 1 | a0001c0001t0003g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.543+514G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66804704 | |||||||
| chr11:66804793 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.543+603C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66804793 | |||||||
| chr11:66805040 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.543+850C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805040 | |||||||
| chr11:66805156 | C | T | 2 | a0001c0002t0001g0009 a0001c0002t0001g0196 |
2 | HG01433.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.543+966C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805156 | |||||||
| chr11:66805413 | A | G | 2 | a0001c0001t0002g0146 a0001c0001t0002g0164 |
2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.543+1223A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805413 | |||||||
| chr11:66805413 | ATGTC | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+1229_543+1232d others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 66805413 | ||||||
| chr11:66805425 | A | G | 1 | a0001c0001t0002g0124 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.543+1235A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805425 | |||||||
| chr11:66805453 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.543+1263G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805453 | |||||||
| chr11:66805470 | T | C | 1 | a0001c0002t0001g0211 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.543+1280T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805470 | |||||||
| chr11:66805737 | A | G | 7 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+1547A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805737 | |||||||
| chr11:66805931 | C | G | 2 | a0001c0001t0001g0056 a0001c0001t0003g0201 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.543+1741C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66805931 | |||||||
| chr11:66806346 | C | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+2156C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66806346 | |||||||
| chr11:66806760 | TA | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+2579delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 66806760 | ||||||
| chr11:66806761 | A | G | 2 | a0001c0001t0002g0132 a0001c0001t0002g0225 |
2 | HG00438.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.543+2571A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66806761 | |||||||
| chr11:66806787 | G | C | 1 | a0001c0002t0001g0026 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.543+2597G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66806787 | |||||||
| chr11:66807209 | A | C | 1 | a0001c0001t0001g0041 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.543+3019A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66807209 | |||||||
| chr11:66807363 | G | A | 1 | a0001c0001t0003g0002 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.543+3173G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66807363 | |||||||
| chr11:66807384 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+3194C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66807384 | |||||||
| chr11:66807531 | A | G | 1 | a0001c0002t0001g0030 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.543+3341A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66807531 | |||||||
| chr11:66807561 | G | A | 7 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+3371G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66807561 | |||||||
| chr11:66807925 | T | C | 1 | a0001c0002t0001g0018 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.543+3735T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66807925 | |||||||
| chr11:66808115 | A | G | 1 | a0001c0001t0002g0170 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.543+3925A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808115 | |||||||
| chr11:66808148 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.543+3958G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808148 | |||||||
| chr11:66808278 | T | C | 1 | a0001c0001t0002g0183 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.543+4088T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808278 | |||||||
| chr11:66808537 | T | A | 3 | a0001c0001t0003g0001 a0001c0001t0003g0137 a0001c0001t0003g0150 |
3 | HG00099.hp1 HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.543+4347T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808537 | |||||||
| chr11:66808779 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+4589A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808779 | |||||||
| chr11:66808865 | CAAAAAGA | C | 4 | a0001c0001t0001g0204 a0001c0001t0001g0232 a0001c0001t0001g0234 others(1): Show |
4 | HG02071.hp2 HG02602.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+4676_543+4682d others(9): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808865 | |||||||
| chr11:66808946 | G | C | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+4756G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66808946 | |||||||
| chr11:66809129 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.544-4736A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66809129 | |||||||
| chr11:66809158 | A | G | 2 | a0001c0001t0002g0191 a0001c0001t0002g0221 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.544-4707A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66809158 | |||||||
| chr11:66809395 | C | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.544-4470C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66809395 | |||||||
| chr11:66809792 | C | T | 1 | a0001c0001t0004g0084 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.544-4073C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66809792 | |||||||
| chr11:66809799 | G | C | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-4066G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66809799 | |||||||
| chr11:66809886 | A | G | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544-3979A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66809886 | |||||||
| chr11:66810308 | C | G | 1 | a0001c0002t0002g0065 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.544-3557C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810308 | |||||||
| chr11:66810426 | G | A | 72 | a0001c0001t0001g0032 a0001c0001t0001g0041 a0001c0001t0001g0042 others(69): Show |
72 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.544-3439G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810426 | |||||||
| chr11:66810462 | A | G | 1 | a0001c0002t0001g0213 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.544-3403A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810462 | |||||||
| chr11:66810538 | G | A | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544-3327G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810538 | |||||||
| chr11:66810549 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-3316A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810549 | |||||||
| chr11:66810592 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-3273A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810592 | |||||||
| chr11:66810799 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.544-3066A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810799 | |||||||
| chr11:66810863 | TC | T | 4 | a0001c0001t0003g0166 a0001c0001t0003g0172 a0001c0001t0003g0176 others(1): Show |
4 | HG01074.hp1 HG01175.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-3001delC | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66810863 | |||||||
| chr11:66810897 | A | AG | 131 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0041 others(128): Show |
131 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.544-2966dupG | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 66810897 | ||||||
| chr11:66811164 | G | A | 131 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0041 others(128): Show |
131 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.544-2701G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811164 | |||||||
| chr11:66811198 | C | T | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0112 |
3 | HG02965.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.544-2667C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811198 | |||||||
| chr11:66811290 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.544-2575T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811290 | |||||||
| chr11:66811648 | T | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-2217T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811648 | |||||||
| chr11:66811810 | C | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-2055C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811810 | |||||||
| chr11:66811947 | A | G | 2 | a0001c0001t0004g0184 a0001c0001t0004g0185 |
2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.544-1918A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811947 | |||||||
| chr11:66811972 | A | T | 6 | a0001c0001t0001g0204 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-1893A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66811972 | |||||||
| chr11:66812094 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.544-1771A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812094 | |||||||
| chr11:66812101 | A | G | 1 | a0001c0002t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.544-1764A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812101 | |||||||
| chr11:66812185 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0094 a0001c0002t0013g0071 a0002c0003t0005g0237 others(1): Show |
4 | HG01168.hp1 HG02615.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-1671_544-1670i others(13): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 66812185 | ||||||
| chr11:66812185 | C | CTTTTTTT others(5): Show |
126 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0041 others(123): Show |
126 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.544-1671_544-1670i others(14): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 66812185 | ||||||
| chr11:66812185 | C | CTTTTTTT others(6): Show |
1 | a0001c0002t0001g0075 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.544-1671_544-1670i others(15): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr11 | 66812185 | ||||||
| chr11:66812232 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-1633A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812232 | |||||||
| chr11:66812418 | C | T | 3 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 |
3 | HG02723.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.544-1447C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812418 | |||||||
| chr11:66812466 | G | A | 1 | a0002c0003t0005g0120 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.544-1399G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812466 | |||||||
| chr11:66812848 | T | C | 1 | a0001c0001t0002g0126 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.544-1017T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812848 | |||||||
| chr11:66812940 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.544-925A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66812940 | |||||||
| chr11:66813265 | A | G | 5 | a0001c0001t0002g0136 a0001c0001t0002g0143 a0001c0001t0002g0146 others(2): Show |
5 | NA18968.hp2 NA18977.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.544-600A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66813265 | |||||||
| chr11:66813597 | G | A | 1 | a0001c0002t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.544-268G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66813597 | |||||||
| chr11:66813668 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.544-197G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66813668 | |||||||
| chr11:66813711 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0002g0190 |
2 | HG02165.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.544-154C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 7/14 | chr11 | 66813711 | |||||||
| chr11:66814202 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.694+187C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66814202 | |||||||
| chr11:66814206 | C | CA | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.694+193dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr11 | 66814206 | ||||||
| chr11:66814328 | G | A | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG00280.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.694+313G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66814328 | |||||||
| chr11:66814555 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.694+540A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66814555 | |||||||
| chr11:66814565 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.694+550G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66814565 | |||||||
| chr11:66814739 | A | G | 48 | a0001c0001t0001g0012 a0001c0001t0001g0197 a0001c0002t0001g0003 others(45): Show |
48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.694+724A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66814739 | |||||||
| chr11:66814971 | C | T | 3 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 |
3 | HG02723.hp1 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.694+956C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66814971 | |||||||
| chr11:66815605 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0003g0201 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.695-448A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66815605 | |||||||
| chr11:66815624 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG02080.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.695-429G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66815624 | |||||||
| chr11:66816031 | C | T | 1 | a0001c0001t0002g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.695-22C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 8/14 | chr11 | 66816031 | |||||||
| chr11:66816288 | A | G | 48 | a0001c0001t0001g0012 a0001c0001t0001g0197 a0001c0002t0001g0003 others(45): Show |
48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.841+89A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66816288 | |||||||
| chr11:66816308 | T | G | 163 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(160): Show |
163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.841+109T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66816308 | |||||||
| chr11:66816480 | T | C | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.841+281T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66816480 | |||||||
| chr11:66816567 | T | TTTAAATT others(7): Show |
1 | a0001c0001t0001g0230 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.841+371_841+384dup others(14): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66816567 | ||||||
| chr11:66816769 | G | A | 1 | a0004c0005t0005g0236 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.841+570G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66816769 | |||||||
| chr11:66817029 | T | G | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.841+830T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66817029 | |||||||
| chr11:66817155 | G | GAAATAAA others(3): Show |
1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.841+976_841+985dup others(10): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66817155 | ||||||
| chr11:66817155 | G | GAAATAAA others(8): Show |
2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.841+971_841+985dup others(15): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66817155 | ||||||
| chr11:66817155 | G | GAAATAAA others(13): Show |
3 | a0002c0003t0005g0118 a0002c0003t0005g0237 a0002c0003t0005g0238 |
3 | HG01884.hp1 HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.841+966_841+985dup others(20): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66817155 | ||||||
| chr11:66817155 | G | GAAATAAA others(18): Show |
4 | a0002c0003t0005g0120 a0004c0005t0005g0119 a0004c0005t0005g0236 others(1): Show |
4 | HG01243.hp1 HG02647.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.841+961_841+985dup others(25): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66817155 | ||||||
| chr11:66817267 | G | C | 1 | a0001c0002t0001g0067 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.841+1068G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66817267 | |||||||
| chr11:66817564 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.841+1365G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66817564 | |||||||
| chr11:66817814 | T | G | 1 | a0001c0002t0001g0040 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.841+1615T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66817814 | |||||||
| chr11:66818106 | C | A | 1 | a0001c0002t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.841+1907C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66818106 | |||||||
| chr11:66818159 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.841+1960A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66818159 | |||||||
| chr11:66818260 | C | T | 1 | a0001c0002t0001g0024 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.841+2061C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66818260 | |||||||
| chr11:66818500 | C | G | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.841+2301C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66818500 | |||||||
| chr11:66818553 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.841+2354G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66818553 | |||||||
| chr11:66819154 | G | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.842-2489G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819154 | |||||||
| chr11:66819550 | C | T | 1 | a0001c0002t0001g0023 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.842-2093C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819550 | |||||||
| chr11:66819597 | C | T | 2 | a0001c0001t0002g0156 a0001c0001t0002g0220 |
2 | NA18970.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.842-2046C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819597 | |||||||
| chr11:66819602 | C | G | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.842-2041C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819602 | |||||||
| chr11:66819615 | A | G | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.842-2028A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819615 | |||||||
| chr11:66819621 | C | T | 1 | a0001c0001t0004g0081 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.842-2022C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819621 | |||||||
| chr11:66819728 | C | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.842-1915C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819728 | |||||||
| chr11:66819897 | CT | C | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.842-1744delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66819897 | ||||||
| chr11:66819904 | TA | T | 227 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(224): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.842-1717delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66819904 | ||||||
| chr11:66819906 | A | T | 2 | a0001c0001t0001g0242 a0001c0001t0003g0243 |
2 | HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.842-1737A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66819906 | |||||||
| chr11:66820129 | G | A | 1 | a0001c0001t0004g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.842-1514G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66820129 | |||||||
| chr11:66820148 | A | C | 1 | a0001c0001t0001g0235 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.842-1495A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66820148 | |||||||
| chr11:66820864 | CTTTCTTA others(11): Show |
C | 1 | a0001c0002t0001g0020 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.842-778_842-761del others(18): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66820864 | |||||||
| chr11:66821041 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.842-602C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66821041 | |||||||
| chr11:66821286 | AT | A | 219 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0041 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.842-338delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr11 | 66821286 | ||||||
| chr11:66821413 | G | A | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.842-230G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66821413 | |||||||
| chr11:66821497 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.842-146G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 9/14 | chr11 | 66821497 | |||||||
| chr11:66821907 | G | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0210 |
2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.963+143G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 10/14 | chr11 | 66821907 | |||||||
| chr11:66821969 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.963+205T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 10/14 | chr11 | 66821969 | |||||||
| chr11:66821988 | T | G | 1 | a0001c0001t0002g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.963+224T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 10/14 | chr11 | 66821988 | |||||||
| chr11:66822396 | C | A | 1 | a0001c0001t0002g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.964-168C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 10/14 | chr11 | 66822396 | |||||||
| chr11:66822400 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-164A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 10/14 | chr11 | 66822400 | |||||||
| chr11:66822928 | C | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074+254C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66822928 | |||||||
| chr11:66822997 | T | TA | 18 | a0001c0001t0001g0055 a0001c0001t0001g0131 a0001c0001t0001g0139 others(15): Show |
18 | HG00423.hp2 HG01109.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.1074+338dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66822997 | ||||||
| chr11:66822997 | TA | T | 7 | a0001c0001t0001g0012 a0002c0003t0005g0118 a0002c0003t0005g0120 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1074+338delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66822997 | ||||||
| chr11:66823025 | T | C | 1 | a0001c0001t0004g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1074+351T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66823025 | |||||||
| chr11:66823084 | C | T | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1074+410C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66823084 | |||||||
| chr11:66823294 | C | CA | 14 | a0001c0001t0001g0036 a0001c0001t0001g0060 a0001c0001t0001g0113 others(11): Show |
14 | HG00621.hp2 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1074+641dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66823294 | ||||||
| chr11:66823384 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1074+710T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66823384 | |||||||
| chr11:66823593 | G | A | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1074+919G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66823593 | |||||||
| chr11:66823790 | C | G | 14 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
14 | HG00438.hp2 HG00621.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1074+1116C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66823790 | |||||||
| chr11:66824276 | G | A | 6 | a0001c0001t0002g0136 a0001c0001t0002g0146 a0001c0001t0002g0162 others(3): Show |
6 | NA18968.hp2 NA18982.hp2 NA18999.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+1602G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66824276 | |||||||
| chr11:66824419 | A | T | 1 | a0001c0001t0002g0216 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1074+1745A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66824419 | |||||||
| chr11:66824420 | T | A | 1 | a0001c0001t0002g0174 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1074+1746T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66824420 | |||||||
| chr11:66824420 | T | TTTA | 16 | a0001c0001t0001g0046 a0001c0001t0001g0098 a0001c0001t0001g0197 others(13): Show |
16 | HG00738.hp2 HG01928.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1074+1787_1074+178 others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | ||||||
| chr11:66824420 | T | TTTATTA | 4 | a0001c0001t0001g0100 a0001c0001t0002g0132 a0001c0001t0002g0187 others(1): Show |
4 | HG00438.hp1 HG01433.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+1784_1074+178 others(10): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | ||||||
| chr11:66824420 | TTTA | T | 59 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0035 others(56): Show |
59 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1074+1787_1074+178 others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | ||||||
| chr11:66824420 | TTTATTA | T | 16 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0055 others(13): Show |
16 | HG00408.hp1 HG00423.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1074+1784_1074+178 others(10): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | ||||||
| chr11:66824420 | TTTATTAT others(2): Show |
T | 48 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0231 others(45): Show |
48 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1074+1781_1074+178 others(13): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | ||||||
| chr11:66824420 | TTTATTAT others(5): Show |
T | 1 | a0001c0002t0001g0196 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1074+1778_1074+178 others(16): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | ||||||
| chr11:66824420 | TTTATTAT others(8): Show |
T | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1074+1775_1074+178 others(19): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66824420 | ||||||
| chr11:66824528 | G | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1074+1854G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66824528 | |||||||
| chr11:66825036 | G | A | 6 | a0001c0001t0001g0204 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074+2362G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825036 | |||||||
| chr11:66825110 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1074+2436C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825110 | |||||||
| chr11:66825158 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1074+2484C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825158 | |||||||
| chr11:66825187 | G | A | 1 | a0001c0002t0001g0010 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1074+2513G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825187 | |||||||
| chr11:66825211 | A | G | 4 | a0001c0001t0002g0177 a0001c0001t0002g0178 a0001c0001t0002g0179 others(1): Show |
4 | NA18943.hp2 NA18990.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074+2537A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825211 | |||||||
| chr11:66825362 | G | C | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1074+2688G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825362 | |||||||
| chr11:66825446 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1074+2772G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825446 | |||||||
| chr11:66825462 | G | T | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1074+2788G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825462 | |||||||
| chr11:66825478 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1075-2788C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825478 | |||||||
| chr11:66825495 | C | CA | 53 | a0001c0001t0001g0012 a0001c0001t0001g0078 a0001c0001t0001g0117 others(50): Show |
53 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1075-2760dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66825495 | ||||||
| chr11:66825579 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075-2687G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825579 | |||||||
| chr11:66825616 | T | C | 10 | a0001c0001t0004g0081 a0001c0001t0004g0082 a0001c0001t0004g0121 others(7): Show |
10 | HG01243.hp2 HG01934.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1075-2650T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825616 | |||||||
| chr11:66825841 | C | CT | 7 | a0001c0001t0001g0182 a0001c0001t0002g0221 a0001c0001t0002g0223 others(4): Show |
7 | HG01109.hp2 HG02738.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-2411dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66825841 | ||||||
| chr11:66825982 | C | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075-2284C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66825982 | |||||||
| chr11:66826045 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0096 a0001c0001t0001g0101 |
3 | HG02257.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1075-2221G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826045 | |||||||
| chr11:66826078 | C | T | 1 | a0001c0002t0013g0071 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1075-2188C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826078 | |||||||
| chr11:66826210 | A | G | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1075-2056A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826210 | |||||||
| chr11:66826255 | T | A | 1 | a0001c0001t0011g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1075-2011T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826255 | |||||||
| chr11:66826298 | T | C | 1 | a0001c0001t0004g0081 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1075-1968T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826298 | |||||||
| chr11:66826323 | T | G | 1 | a0001c0001t0004g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1075-1943T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826323 | |||||||
| chr11:66826477 | A | T | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1075-1789A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826477 | |||||||
| chr11:66826691 | AT | A | 9 | a0001c0001t0001g0055 a0001c0001t0001g0131 a0001c0001t0001g0139 others(6): Show |
9 | HG00423.hp2 HG02523.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1075-1567delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66826691 | ||||||
| chr11:66826709 | T | C | 1 | a0001c0007t0004g0188 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1075-1557T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826709 | |||||||
| chr11:66826760 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1075-1506G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66826760 | |||||||
| chr11:66826981 | C | CT | 144 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0035 others(141): Show |
144 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.1075-1268dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66826981 | ||||||
| chr11:66826981 | C | CTT | 7 | a0001c0001t0001g0056 a0001c0001t0001g0093 a0001c0001t0001g0235 others(4): Show |
7 | HG00408.hp1 HG01175.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-1269_1075-126 others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66826981 | ||||||
| chr11:66827042 | C | T | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1075-1224C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66827042 | |||||||
| chr11:66827207 | C | T | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075-1059C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66827207 | |||||||
| chr11:66827955 | ACT | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0096 a0001c0001t0001g0101 |
3 | HG02257.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1075-308_1075-307d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66827955 | ||||||
| chr11:66827966 | G | GA | 123 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0036 others(120): Show |
123 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1075-273dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66827966 | ||||||
| chr11:66827966 | G | GAA | 8 | a0001c0001t0001g0046 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
8 | HG01361.hp2 HG01928.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1075-274_1075-273d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66827966 | ||||||
| chr11:66827966 | GAA | G | 7 | a0001c0001t0003g0243 a0002c0003t0005g0118 a0002c0003t0005g0120 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1075-274_1075-273d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66827966 | ||||||
| chr11:66827966 | GAAAAAAA others(3): Show |
G | 3 | a0001c0001t0001g0231 a0001c0001t0004g0081 a0001c0001t0004g0082 |
3 | HG01243.hp2 HG02630.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1075-282_1075-273d others(12): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr11 | 66827966 | ||||||
| chr11:66827992 | A | T | 1 | a0002c0003t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1075-274A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66827992 | |||||||
| chr11:66828181 | C | G | 1 | a0001c0001t0002g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1075-85C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 11/14 | chr11 | 66828181 | |||||||
| chr11:66828393 | G | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0096 a0001c0001t0001g0101 |
3 | HG02257.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1173+29G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828393 | |||||||
| chr11:66828433 | G | T | 1 | a0002c0003t0005g0237 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1173+69G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828433 | |||||||
| chr11:66828508 | A | G | 24 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(21): Show |
24 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.1173+144A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828508 | |||||||
| chr11:66828574 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0096 |
2 | HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1173+210G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828574 | |||||||
| chr11:66828611 | C | T | 3 | a0001c0001t0002g0134 a0001c0001t0002g0167 a0001c0001t0002g0168 |
3 | NA18941.hp2 NA18962.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1173+247C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828611 | |||||||
| chr11:66828621 | G | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1173+257G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828621 | |||||||
| chr11:66828733 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0003g0201 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1173+369G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828733 | |||||||
| chr11:66828966 | GTGTTTTT | G | 3 | a0001c0001t0002g0134 a0001c0001t0002g0167 a0001c0001t0002g0168 |
3 | NA18941.hp2 NA18962.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1173+611_1173+617d others(9): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66828966 | ||||||
| chr11:66828975 | G | GT | 43 | a0001c0001t0001g0050 a0001c0001t0001g0053 a0001c0001t0001g0078 others(40): Show |
43 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.1173+625dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66828975 | ||||||
| chr11:66828975 | G | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0210 |
3 | HG02630.hp2 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1173+611G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66828975 | |||||||
| chr11:66828975 | GT | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+625delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66828975 | ||||||
| chr11:66829041 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1173+677G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829041 | |||||||
| chr11:66829068 | C | CA | 34 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0054 others(31): Show |
34 | HG00280.hp1 HG00280.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1173+731dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66829068 | ||||||
| chr11:66829068 | CA | C | 10 | a0001c0001t0001g0043 a0001c0001t0001g0208 a0001c0001t0002g0220 others(7): Show |
10 | HG01243.hp2 HG01515.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1173+731delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66829068 | ||||||
| chr11:66829068 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0189 a0001c0001t0002g0190 |
2 | HG02165.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1173+719_1173+731d others(15): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66829068 | ||||||
| chr11:66829313 | C | T | 6 | a0001c0001t0001g0204 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
6 | HG01361.hp2 HG02071.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.1173+949C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829313 | |||||||
| chr11:66829341 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1173+977C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829341 | |||||||
| chr11:66829414 | A | G | 3 | a0001c0001t0007g0226 a0001c0001t0007g0227 a0001c0001t0007g0228 |
3 | HG01123.hp1 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1173+1050A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829414 | |||||||
| chr11:66829461 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1173+1097G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829461 | |||||||
| chr11:66829585 | A | AG | 58 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0078 others(55): Show |
58 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1173+1221_1173+122 others(5): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829585 | |||||||
| chr11:66829732 | T | C | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1173+1368T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829732 | |||||||
| chr11:66829763 | C | G | 5 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+1399C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829763 | |||||||
| chr11:66829773 | C | T | 1 | a0001c0001t0002g0143 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1173+1409C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66829773 | |||||||
| chr11:66830056 | C | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+1692C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830056 | |||||||
| chr11:66830115 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+1751A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830115 | |||||||
| chr11:66830266 | C | T | 5 | a0001c0001t0006g0080 a0001c0001t0006g0087 a0001c0001t0006g0089 others(2): Show |
5 | HG01934.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+1902C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830266 | |||||||
| chr11:66830306 | C | T | 1 | a0001c0001t0002g0133 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1173+1942C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830306 | |||||||
| chr11:66830477 | A | C | 1 | a0001c0001t0002g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1173+2113A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830477 | |||||||
| chr11:66830559 | T | C | 1 | a0001c0002t0001g0067 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1173+2195T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830559 | |||||||
| chr11:66830637 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1173+2273C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830637 | |||||||
| chr11:66830982 | G | T | 1 | a0001c0001t0002g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1173+2618G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66830982 | |||||||
| chr11:66831071 | A | C | 6 | a0001c0001t0004g0240 a0001c0001t0006g0080 a0001c0001t0006g0087 others(3): Show |
6 | HG01934.hp1 HG02109.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+2707A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66831071 | |||||||
| chr11:66831180 | C | T | 27 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(24): Show |
27 | HG00408.hp1 HG00423.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.1173+2816C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66831180 | |||||||
| chr11:66831351 | C | T | 1 | a0001c0001t0003g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1173+2987C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66831351 | |||||||
| chr11:66831398 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0001g0208 |
3 | HG00408.hp1 NA18966.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1173+3034T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66831398 | |||||||
| chr11:66831733 | C | T | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1173+3369C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66831733 | |||||||
| chr11:66831889 | T | C | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1173+3525T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66831889 | |||||||
| chr11:66831996 | C | CA | 80 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0041 others(77): Show |
80 | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.1173+3652dupA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66831996 | ||||||
| chr11:66831996 | CA | C | 8 | a0001c0001t0001g0096 a0001c0001t0001g0235 a0001c0001t0002g0146 others(5): Show |
8 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1173+3652delA | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66831996 | ||||||
| chr11:66832017 | C | A | 2 | a0001c0001t0001g0204 a0001c0001t0004g0081 |
2 | HG01243.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1173+3653C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832017 | |||||||
| chr11:66832259 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+3895G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832259 | |||||||
| chr11:66832276 | A | C | 1 | a0001c0001t0002g0146 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1173+3912A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832276 | |||||||
| chr11:66832366 | C | G | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1173+4002C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832366 | |||||||
| chr11:66832389 | C | T | 6 | a0001c0001t0003g0002 a0001c0001t0003g0137 a0001c0001t0003g0166 others(3): Show |
6 | HG01074.hp1 HG01175.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1173+4025C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832389 | |||||||
| chr11:66832402 | C | A | 1 | a0001c0001t0002g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1173+4038C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832402 | |||||||
| chr11:66832851 | G | T | 1 | a0001c0002t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1173+4487G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66832851 | |||||||
| chr11:66833040 | C | CT | 35 | a0001c0001t0001g0036 a0001c0001t0001g0054 a0001c0001t0001g0058 others(32): Show |
35 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1173+4701dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66833040 | ||||||
| chr11:66833040 | CT | C | 15 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0091 others(12): Show |
15 | HG00323.hp1 HG01243.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1173+4701delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66833040 | ||||||
| chr11:66833040 | CTTTT | C | 5 | a0001c0001t0006g0080 a0001c0001t0006g0087 a0001c0001t0006g0089 others(2): Show |
5 | HG01934.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+4698_1173+470 others(8): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66833040 | ||||||
| chr11:66833101 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+4737G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66833101 | |||||||
| chr11:66833488 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0003g0201 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1174-4882C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66833488 | |||||||
| chr11:66833567 | C | T | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174-4803C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66833567 | |||||||
| chr11:66833621 | T | C | 41 | a0001c0001t0001g0032 a0001c0001t0001g0057 a0001c0001t0001g0058 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.1174-4749T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66833621 | |||||||
| chr11:66833729 | C | G | 1 | a0001c0002t0001g0194 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1174-4641C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66833729 | |||||||
| chr11:66833880 | G | A | 1 | a0001c0002t0001g0203 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1174-4490G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66833880 | |||||||
| chr11:66834363 | A | G | 1 | a0001c0001t0002g0133 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1174-4007A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66834363 | |||||||
| chr11:66834421 | T | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1174-3949T>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66834421 | |||||||
| chr11:66834437 | C | T | 1 | a0001c0002t0001g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1174-3933C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66834437 | |||||||
| chr11:66834603 | T | A | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1174-3767T>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66834603 | |||||||
| chr11:66834628 | C | T | 163 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(160): Show |
163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1174-3742C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66834628 | |||||||
| chr11:66834972 | G | A | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174-3398G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66834972 | |||||||
| chr11:66835022 | C | T | 1 | a0001c0001t0012g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1174-3348C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66835022 | |||||||
| chr11:66835309 | GTTTC | G | 30 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(27): Show |
30 | HG00280.hp1 HG00609.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1174-3053_1174-305 others(8): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66835309 | ||||||
| chr11:66835483 | A | G | 2 | a0001c0001t0002g0132 a0001c0001t0002g0225 |
2 | HG00438.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1174-2887A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66835483 | |||||||
| chr11:66835658 | G | C | 2 | a0001c0001t0001g0056 a0001c0001t0003g0201 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1174-2712G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66835658 | |||||||
| chr11:66835772 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1174-2598T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66835772 | |||||||
| chr11:66835809 | G | A | 8 | a0001c0001t0002g0126 a0001c0001t0002g0129 a0001c0001t0002g0145 others(5): Show |
8 | HG00408.hp2 NA18939.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174-2561G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66835809 | |||||||
| chr11:66836028 | A | G | 2 | a0001c0001t0004g0084 a0001c0001t0004g0085 |
2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1174-2342A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836028 | |||||||
| chr11:66836240 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1174-2130G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836240 | |||||||
| chr11:66836432 | A | G | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1174-1938A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836432 | |||||||
| chr11:66836545 | T | C | 4 | a0001c0001t0009g0004 a0003c0004t0008g0062 a0003c0004t0008g0063 others(1): Show |
4 | HG01109.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-1825T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836545 | |||||||
| chr11:66836564 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1174-1806T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836564 | |||||||
| chr11:66836625 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1174-1745G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836625 | |||||||
| chr11:66836627 | A | G | 1 | a0001c0001t0002g0173 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1174-1743A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836627 | |||||||
| chr11:66836699 | G | A | 10 | a0001c0001t0009g0004 a0002c0003t0005g0118 a0002c0003t0005g0120 others(7): Show |
10 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174-1671G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836699 | |||||||
| chr11:66836700 | A | AT | 157 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(154): Show |
157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1174-1652dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66836700 | ||||||
| chr11:66836700 | A | ATT | 73 | a0001c0001t0001g0032 a0001c0001t0001g0053 a0001c0001t0001g0057 others(70): Show |
73 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1174-1653_1174-165 others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66836700 | ||||||
| chr11:66836700 | A | ATTT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | HG00423.hp1 HG01496.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-1654_1174-165 others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66836700 | ||||||
| chr11:66836728 | T | C | 4 | a0001c0001t0009g0004 a0003c0004t0008g0062 a0003c0004t0008g0063 others(1): Show |
4 | HG01109.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1174-1642T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836728 | |||||||
| chr11:66836962 | G | A | 1 | a0001c0001t0009g0004 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1174-1408G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836962 | |||||||
| chr11:66836973 | A | G | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-1397A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66836973 | |||||||
| chr11:66837252 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1174-1118G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66837252 | |||||||
| chr11:66837445 | A | AT | 50 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(47): Show |
50 | HG00408.hp1 HG00423.hp1 HG01123.hp1 others(47): Show |
intron_variant | MODIFIER | c.1174-907dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66837445 | ||||||
| chr11:66837445 | A | ATT | 5 | a0001c0001t0001g0032 a0001c0001t0001g0091 a0001c0001t0001g0106 others(2): Show |
5 | HG01109.hp2 HG03098.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.1174-908_1174-907d others(4): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr11 | 66837445 | ||||||
| chr11:66837510 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0207 |
2 | NA18945.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1174-860T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66837510 | |||||||
| chr11:66837660 | G | A | 6 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(3): Show |
6 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-710G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66837660 | |||||||
| chr11:66837872 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1174-498C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66837872 | |||||||
| chr11:66837939 | A | C | 10 | a0001c0002t0001g0007 a0001c0002t0001g0020 a0001c0002t0001g0031 others(7): Show |
10 | HG00621.hp1 HG02132.hp2 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.1174-431A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66837939 | |||||||
| chr11:66838212 | G | T | 1 | a0001c0002t0001g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1174-158G>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66838212 | |||||||
| chr11:66838321 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1174-49G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 12/14 | chr11 | 66838321 | |||||||
| chr11:66838475 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0003g0201 |
2 | HG01884.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1249+30G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66838475 | |||||||
| chr11:66838518 | A | C | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1249+73A>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66838518 | |||||||
| chr11:66839326 | T | C | 1 | a0001c0002t0001g0074 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1249+881T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66839326 | |||||||
| chr11:66839499 | C | A | 1 | a0001c0002t0001g0076 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1249+1054C>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66839499 | |||||||
| chr11:66839583 | G | A | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1249+1138G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66839583 | |||||||
| chr11:66840184 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1249+1739A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66840184 | |||||||
| chr11:66840282 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1249+1837C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66840282 | |||||||
| chr11:66840314 | C | T | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG00280.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1249+1869C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66840314 | |||||||
| chr11:66840391 | C | G | 1 | a0005c0008t0002g0165 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1249+1946C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66840391 | |||||||
| chr11:66840530 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1249+2085C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66840530 | |||||||
| chr11:66840764 | C | T | 2 | a0003c0004t0008g0062 a0003c0004t0008g0063 |
2 | HG01109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1250-2085C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66840764 | |||||||
| chr11:66841050 | G | C | 208 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(205): Show |
208 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.1250-1799G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841050 | |||||||
| chr11:66841104 | C | G | 2 | a0001c0001t0002g0044 a0001c0001t0002g0045 |
2 | HG00280.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1250-1745C>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841104 | |||||||
| chr11:66841110 | A | AT | 77 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0053 others(74): Show |
77 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1250-1715dupT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 66841110 | ||||||
| chr11:66841110 | A | T | 1 | a0001c0002t0001g0033 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1250-1739A>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841110 | |||||||
| chr11:66841110 | AT | A | 14 | a0001c0001t0001g0036 a0001c0001t0001g0186 a0001c0001t0002g0133 others(11): Show |
14 | HG00621.hp2 HG01074.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1250-1715delT | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 66841110 | ||||||
| chr11:66841110 | ATT | A | 7 | a0002c0003t0005g0118 a0002c0003t0005g0120 a0002c0003t0005g0237 others(4): Show |
7 | HG01243.hp1 HG01884.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1250-1716_1250-171 others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 66841110 | ||||||
| chr11:66841406 | G | A | 1 | a0002c0003t0005g0118 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1250-1443G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841406 | |||||||
| chr11:66841406 | G | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0029 |
2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1250-1443G>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841406 | |||||||
| chr11:66841417 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1250-1432A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841417 | |||||||
| chr11:66841520 | T | C | 163 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0028 others(160): Show |
163 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.1250-1329T>C | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841520 | |||||||
| chr11:66841682 | A | AGGT | 4 | a0001c0001t0009g0004 a0003c0004t0008g0062 a0003c0004t0008g0063 others(1): Show |
4 | HG01109.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1250-1162_1250-116 others(7): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 66841682 | ||||||
| chr11:66841818 | C | T | 132 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0041 others(129): Show |
132 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1250-1031C>T | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66841818 | |||||||
| chr11:66841850 | T | TTTAC | 4 | a0001c0001t0009g0004 a0003c0004t0008g0062 a0003c0004t0008g0063 others(1): Show |
4 | HG01109.hp2 HG03098.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1250-997_1250-996i others(6): Show |
C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr11 | 66841850 | ||||||
| chr11:66842281 | A | G | 4 | a0001c0001t0001g0239 a0001c0001t0001g0242 a0001c0001t0003g0243 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250-568A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66842281 | |||||||
| chr11:66842452 | A | G | 1 | a0007c0006t0009g0247 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1250-397A>G | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66842452 | |||||||
| chr11:66842500 | G | A | 4 | a0001c0001t0006g0080 a0001c0001t0006g0087 a0001c0001t0006g0089 others(1): Show |
4 | HG01934.hp1 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250-349G>A | C11orf80 | ENSG00000173715.19 | transcript | ENST00000540737.7 | protein_coding | 13/14 | chr11 | 66842500 |