Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 389400 |
| ensemblid | ENSG00000187871.2 |
| hgncid | 32789 |
| symbol | GFRAL |
| name | GDNF family receptor alpha like |
| refseq_nuc | NM_207410.2 |
| refseq_prot | NP_997293.2 |
| ensembl_nuc | ENST00000340465.2 |
| ensembl_prot | ENSP00000343636.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 55327469 |
| end | 55402493 |
| strand | + |
| ver | v1.2 |
| region | chr6:55327469-55402493 |
| region5000 | chr6:55322469-55407493 |
| regionname0 | GFRAL_chr6_55327469_55402493 |
| regionname5000 | GFRAL_chr6_55322469_55407493 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 394 | 191 | 32 | 42 | 100 | 6 | 10 | 83 | GFRAL_chr6_55322469_55407493 | GFRAL | MIVFI others(389): Show |
chr6 | 55322469 | 55407493 |
| a0002 | 0/0 | 394 | 81 | 19 | 12 | 33 | 2 | 15 | 25 | GFRAL_chr6_55322469_55407493 | GFRAL | MIVFI others(389): Show |
chr6 | 55322469 | 55407493 |
| a0003 | 0/0 | 394 | 67 | 22 | 7 | 24 | 2 | 12 | 14 | GFRAL_chr6_55322469_55407493 | GFRAL | MIVFI others(389): Show |
chr6 | 55322469 | 55407493 |
| a0004 | 1/0 | 394 | 45 | 20 | 6 | 13 | 4 | 1 | 10 | GFRAL_chr6_55322469_55407493 | GFRAL | MIVFI others(389): Show |
chr6 | 55322469 | 55407493 |
| a0005 | 0/0 | 394 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | MIVFI others(389): Show |
chr6 | 55322469 | 55407493 |
| a0006 | 0/0 | 394 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | MIVFI others(389): Show |
chr6 | 55322469 | 55407493 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1182 | 182 | 24 | 41 | 100 | 6 | 10 | GFRAL_chr6_55322469_55407493 | GFRAL | ATGAT others(1177): Show |
chr6 | 55322469 | 55407493 | ||
| a0001c0005 | 0/0 | 1182 | 8 | 8 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | ATGAT others(1177): Show |
chr6 | 55322469 | 55407493 | ||
| a0001c0007 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | ATGAT others(1177): Show |
chr6 | 55322469 | 55407493 | ||
| a0002c0002 | 0/0 | 1182 | 80 | 18 | 12 | 33 | 2 | 15 | GFRAL_chr6_55322469_55407493 | GFRAL | ATGAT others(1177): Show |
chr6 | 55322469 | 55407493 | ||
| a0002c0010 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | ATGAT others(1177): Show |
chr6 | 55322469 | 55407493 | ||
| a0003c0003 | 0/0 | 1182 | 67 | 22 | 7 | 24 | 2 | 12 | GFRAL_chr6_55322469_55407493 | GFRAL | ATGAT others(1177): Show |
chr6 | 55322469 | 55407493 | ||
| a0004c0004 | 1/0 | 1182 | 44 | 19 | 6 | 13 | 4 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | ATGAT others(1177): Show |
chr6 | 55322469 | 55407493 | ||
| a0004c0008 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | ATGAT others(1177): Show |
chr6 | 55322469 | 55407493 | ||
| a0005c0009 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | ATGAT others(1177): Show |
chr6 | 55322469 | 55407493 | ||
| a0006c0006 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | ATGAT others(1177): Show |
chr6 | 55322469 | 55407493 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1910 | 99 | 3 | 26 | 60 | 4 | 6 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1905): Show |
chr6 | 55322469 | 55407493 |
| a0001c0001t0002 | 0/0 | 1911 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0001c0001t0003 | 0/0 | 1911 | 19 | 15 | 3 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0001c0001t0004 | 0/0 | 1911 | 56 | 2 | 11 | 38 | 2 | 3 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0001c0001t0006 | 0/0 | 1911 | 2 | 2 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0001c0001t0008 | 0/0 | 1910 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1905): Show |
chr6 | 55322469 | 55407493 |
| a0001c0001t0011 | 0/0 | 1874 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1869): Show |
chr6 | 55322469 | 55407493 |
| a0001c0001t0012 | 0/0 | 1911 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0001c0001t0013 | 0/1 | 1909 | 1 | 0 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1904): Show |
chr6 | 55322469 | 55407493 |
| a0001c0005t0003 | 0/0 | 1911 | 6 | 6 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0001c0005t0004 | 0/0 | 1911 | 2 | 2 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0001c0007t0004 | 0/0 | 1911 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0002c0002t0001 | 0/0 | 1910 | 13 | 0 | 3 | 5 | 1 | 4 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1905): Show |
chr6 | 55322469 | 55407493 |
| a0002c0002t0003 | 0/0 | 1911 | 48 | 11 | 3 | 26 | 0 | 8 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0002c0002t0004 | 0/0 | 1911 | 14 | 6 | 5 | 2 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0002c0002t0006 | 0/0 | 1911 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0002c0002t0007 | 0/0 | 1911 | 2 | 0 | 0 | 0 | 0 | 2 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0002c0002t0010 | 0/0 | 1911 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0002c0002t0014 | 0/0 | 1910 | 1 | 0 | 0 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1905): Show |
chr6 | 55322469 | 55407493 |
| a0002c0010t0003 | 0/0 | 1911 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0003c0003t0002 | 0/0 | 1911 | 67 | 22 | 7 | 24 | 2 | 12 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0004c0004t0002 | 1/0 | 1911 | 40 | 15 | 6 | 13 | 4 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0004c0004t0005 | 0/0 | 1947 | 3 | 3 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1942): Show |
chr6 | 55322469 | 55407493 |
| a0004c0004t0009 | 0/0 | 1911 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0004c0008t0002 | 0/0 | 1911 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0005c0009t0002 | 0/0 | 1911 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| a0006c0006t0003 | 0/0 | 1911 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | TTATT others(1906): Show |
chr6 | 55322469 | 55407493 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0006g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0008g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0008g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0011g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0012g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0001t0013g0272 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0005t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0005t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0005t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0005t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0005t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0005t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0005t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0001c0007t0004g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0007g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0010g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0002t0014g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0002c0010t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0003c0003t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0199 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0004t0009g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0004c0008t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0005c0009t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| a0006c0006t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0273 | EUR | FIN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00323 | hp2 | a0004 | c0004 | t0002 | g0222 | EUR | FIN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00408 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00438 | hp2 | a0002 | c0002 | t0003 | g0335 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00544 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00558 | hp1 | a0003 | c0003 | t0002 | g0153 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00621 | hp1 | a0003 | c0003 | t0002 | g0114 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00639 | hp1 | a0003 | c0003 | t0002 | g0142 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00642 | hp1 | a0002 | c0002 | t0003 | g0089 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00642 | hp2 | a0003 | c0003 | t0002 | g0159 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00673 | hp1 | a0002 | c0002 | t0003 | g0077 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00673 | hp2 | a0003 | c0003 | t0002 | g0119 | EAS | CHS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00735 | hp2 | a0004 | c0004 | t0002 | g0276 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0311 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00741 | hp1 | a0003 | c0003 | t0002 | g0138 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01069 | hp2 | a0002 | c0002 | t0004 | g0112 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01070 | hp1 | a0002 | c0002 | t0004 | g0107 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01074 | hp1 | a0002 | c0002 | t0003 | g0090 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01074 | hp2 | a0004 | c0004 | t0002 | g0285 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01106 | hp2 | a0002 | c0002 | t0004 | g0094 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0149 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01169 | hp1 | a0003 | c0003 | t0002 | g0137 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01169 | hp2 | a0001 | c0001 | t0012 | g0297 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0291 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01243 | hp1 | a0002 | c0002 | t0004 | g0111 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01256 | hp2 | a0003 | c0003 | t0002 | g0141 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01346 | hp1 | a0002 | c0002 | t0010 | g0105 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0319 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01358 | hp1 | a0004 | c0004 | t0002 | g0249 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0082 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0122 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01361 | hp2 | a0002 | c0002 | t0004 | g0118 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0288 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0278 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0305 | EUR | IBS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01515 | hp2 | a0004 | c0004 | t0002 | g0019 | EUR | IBS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01516 | hp2 | a0003 | c0003 | t0002 | g0161 | EUR | IBS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01517 | hp1 | a0004 | c0004 | t0002 | g0019 | EUR | IBS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01884 | hp1 | a0004 | c0008 | t0002 | g0227 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01891 | hp1 | a0002 | c0002 | t0004 | g0157 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01934 | hp1 | a0004 | c0004 | t0002 | g0300 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0314 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01952 | hp2 | a0001 | c0007 | t0004 | g0320 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01978 | hp1 | a0004 | c0004 | t0002 | g0279 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01993 | hp1 | a0003 | c0003 | t0002 | g0129 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02040 | hp2 | a0003 | c0003 | t0002 | g0246 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02055 | hp1 | a0002 | c0002 | t0003 | g0088 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02055 | hp2 | a0005 | c0009 | t0002 | g0250 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02074 | hp1 | a0004 | c0004 | t0002 | g0298 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02080 | hp1 | a0004 | c0004 | t0002 | g0032 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02080 | hp2 | a0003 | c0003 | t0002 | g0124 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02129 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0313 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02132 | hp1 | a0003 | c0003 | t0002 | g0013 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02132 | hp2 | a0002 | c0002 | t0003 | g0334 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02135 | hp2 | a0003 | c0003 | t0002 | g0162 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02145 | hp1 | a0003 | c0003 | t0002 | g0252 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02148 | hp1 | a0004 | c0004 | t0002 | g0301 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02165 | hp1 | a0004 | c0004 | t0002 | g0282 | EAS | CDX | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02257 | hp1 | a0004 | c0004 | t0002 | g0206 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0255 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02258 | hp1 | a0004 | c0004 | t0005 | g0204 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02258 | hp2 | a0003 | c0003 | t0002 | g0012 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02280 | hp1 | a0002 | c0002 | t0003 | g0065 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02280 | hp2 | a0002 | c0002 | t0006 | g0125 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0109 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02300 | hp1 | a0006 | c0006 | t0003 | g0258 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0274 | AMR | PEL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02451 | hp1 | a0004 | c0004 | t0002 | g0326 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0040 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02523 | hp1 | a0003 | c0003 | t0002 | g0237 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02523 | hp2 | a0003 | c0003 | t0002 | g0126 | EAS | KHV | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02572 | hp1 | a0003 | c0003 | t0002 | g0238 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02572 | hp2 | a0004 | c0004 | t0002 | g0325 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02602 | hp1 | a0003 | c0003 | t0002 | g0123 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02602 | hp2 | a0002 | c0002 | t0003 | g0074 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02615 | hp1 | a0004 | c0004 | t0002 | g0321 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02615 | hp2 | a0004 | c0004 | t0002 | g0200 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02622 | hp1 | a0003 | c0003 | t0002 | g0066 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02622 | hp2 | a0003 | c0003 | t0002 | g0063 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02630 | hp1 | a0004 | c0004 | t0002 | g0023 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02630 | hp2 | a0004 | c0004 | t0002 | g0198 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02647 | hp1 | a0004 | c0004 | t0002 | g0221 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02683 | hp1 | a0002 | c0002 | t0003 | g0069 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02698 | hp1 | a0003 | c0003 | t0002 | g0241 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02698 | hp2 | a0003 | c0003 | t0002 | g0128 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02717 | hp1 | a0003 | c0003 | t0002 | g0022 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02717 | hp2 | a0004 | c0004 | t0005 | g0203 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0329 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02723 | hp2 | a0003 | c0003 | t0002 | g0103 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02809 | hp1 | a0004 | c0004 | t0002 | g0023 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02809 | hp2 | a0004 | c0004 | t0002 | g0327 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02818 | hp1 | a0003 | c0003 | t0002 | g0012 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02818 | hp2 | a0003 | c0003 | t0002 | g0253 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02886 | hp1 | a0002 | c0002 | t0004 | g0156 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02886 | hp2 | a0002 | c0010 | t0003 | g0235 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02895 | hp1 | a0004 | c0004 | t0002 | g0035 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02896 | hp1 | a0001 | c0005 | t0004 | g0021 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02896 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02897 | hp1 | a0004 | c0004 | t0002 | g0035 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02897 | hp2 | a0001 | c0005 | t0004 | g0021 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02922 | hp1 | a0002 | c0002 | t0003 | g0139 | AFR | ESN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02922 | hp2 | a0002 | c0002 | t0003 | g0254 | AFR | ESN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02965 | hp2 | a0003 | c0003 | t0002 | g0131 | AFR | ESN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0135 | AFR | ESN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02970 | hp2 | a0003 | c0003 | t0002 | g0056 | AFR | ESN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02976 | hp1 | a0003 | c0003 | t0002 | g0022 | AFR | ESN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02976 | hp2 | a0003 | c0003 | t0002 | g0256 | AFR | ESN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0033 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03017 | hp2 | a0004 | c0004 | t0002 | g0165 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03041 | hp1 | a0002 | c0002 | t0004 | g0154 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | GWD | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0219 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0322 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | ESN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | ESN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03209 | hp1 | a0003 | c0003 | t0002 | g0117 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03209 | hp2 | a0004 | c0004 | t0002 | g0328 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03225 | hp1 | a0002 | c0002 | t0003 | g0024 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03239 | hp1 | a0002 | c0002 | t0003 | g0071 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0286 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03453 | hp2 | a0001 | c0005 | t0003 | g0226 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03486 | hp2 | a0003 | c0003 | t0002 | g0116 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0113 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03492 | hp1 | a0002 | c0002 | t0004 | g0106 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0108 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03516 | hp1 | a0004 | c0004 | t0005 | g0202 | AFR | ESN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03516 | hp2 | a0001 | c0005 | t0003 | g0229 | AFR | ESN | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03579 | hp2 | a0004 | c0004 | t0002 | g0201 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03669 | hp1 | a0003 | c0003 | t0002 | g0233 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03669 | hp2 | a0003 | c0003 | t0002 | g0239 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03688 | hp1 | a0002 | c0002 | t0003 | g0011 | SAS | STU | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | STU | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03704 | hp1 | a0003 | c0003 | t0002 | g0240 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0266 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0265 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03710 | hp2 | a0002 | c0002 | t0003 | g0068 | SAS | PJL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03831 | hp2 | a0003 | c0003 | t0002 | g0160 | SAS | BEB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03834 | hp1 | a0002 | c0002 | t0003 | g0236 | SAS | BEB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03834 | hp2 | a0003 | c0003 | t0002 | g0136 | SAS | BEB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03927 | hp2 | a0003 | c0003 | t0002 | g0163 | SAS | BEB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0104 | SAS | BEB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03942 | hp2 | a0002 | c0002 | t0007 | g0061 | SAS | BEB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG04184 | hp1 | a0002 | c0002 | t0007 | g0064 | SAS | BEB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG04184 | hp2 | a0003 | c0003 | t0002 | g0245 | SAS | BEB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG04204 | hp1 | a0003 | c0003 | t0002 | g0127 | SAS | STU | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG04204 | hp2 | a0002 | c0002 | t0003 | g0011 | SAS | STU | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18522 | hp1 | a0001 | c0005 | t0003 | g0230 | AFR | YRI | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18522 | hp2 | a0001 | c0005 | t0003 | g0232 | AFR | YRI | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | CHB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | CHB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18906 | hp1 | a0004 | c0004 | t0002 | g0197 | AFR | YRI | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0120 | AFR | YRI | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18939 | hp1 | a0004 | c0004 | t0002 | g0031 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18939 | hp2 | a0002 | c0002 | t0003 | g0038 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18941 | hp1 | a0002 | c0002 | t0003 | g0059 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18942 | hp1 | a0004 | c0004 | t0002 | g0031 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18944 | hp1 | a0003 | c0003 | t0002 | g0144 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18944 | hp2 | a0002 | c0002 | t0003 | g0062 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18945 | hp2 | a0003 | c0003 | t0002 | g0330 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18946 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18947 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18948 | hp2 | a0003 | c0003 | t0002 | g0013 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18956 | hp1 | a0002 | c0002 | t0003 | g0095 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18960 | hp2 | a0002 | c0002 | t0004 | g0085 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18961 | hp1 | a0002 | c0002 | t0004 | g0083 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18962 | hp2 | a0002 | c0002 | t0003 | g0081 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18963 | hp2 | a0002 | c0002 | t0003 | g0084 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18964 | hp1 | a0003 | c0003 | t0002 | g0140 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18966 | hp2 | a0002 | c0002 | t0003 | g0067 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18968 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18969 | hp1 | a0004 | c0004 | t0002 | g0030 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18970 | hp1 | a0002 | c0002 | t0003 | g0078 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18970 | hp2 | a0004 | c0004 | t0002 | g0034 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18977 | hp1 | a0004 | c0004 | t0002 | g0317 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18980 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18982 | hp1 | a0002 | c0002 | t0003 | g0080 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18983 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18984 | hp1 | a0004 | c0004 | t0002 | g0032 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18986 | hp2 | a0001 | c0001 | t0008 | g0169 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18987 | hp1 | a0002 | c0002 | t0003 | g0072 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18989 | hp1 | a0004 | c0004 | t0002 | g0332 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18993 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18995 | hp2 | a0004 | c0004 | t0002 | g0030 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19001 | hp1 | a0003 | c0003 | t0002 | g0148 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19004 | hp2 | a0003 | c0003 | t0002 | g0242 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19007 | hp2 | a0002 | c0002 | t0003 | g0075 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19009 | hp1 | a0002 | c0002 | t0003 | g0093 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0303 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | LWK | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19030 | hp2 | a0003 | c0003 | t0002 | g0130 | AFR | LWK | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19043 | hp1 | a0003 | c0003 | t0002 | g0132 | AFR | LWK | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19043 | hp2 | a0003 | c0003 | t0002 | g0243 | AFR | LWK | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19056 | hp2 | a0002 | c0002 | t0003 | g0096 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0152 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19064 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19065 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19066 | hp1 | a0004 | c0004 | t0002 | g0034 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19068 | hp1 | a0003 | c0003 | t0002 | g0110 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19074 | hp2 | a0003 | c0003 | t0002 | g0133 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19075 | hp1 | a0002 | c0002 | t0003 | g0073 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19077 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19078 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19080 | hp2 | a0003 | c0003 | t0002 | g0134 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19082 | hp2 | a0002 | c0002 | t0003 | g0039 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19084 | hp2 | a0002 | c0002 | t0003 | g0076 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19085 | hp1 | a0002 | c0002 | t0003 | g0060 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19085 | hp2 | a0004 | c0004 | t0002 | g0299 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19090 | hp1 | a0001 | c0001 | t0008 | g0293 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19240 | hp1 | a0003 | c0003 | t0002 | g0057 | AFR | YRI | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA19240 | hp2 | a0002 | c0002 | t0003 | g0331 | AFR | YRI | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA20129 | hp2 | a0003 | c0003 | t0002 | g0244 | AFR | ASW | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA20752 | hp1 | a0004 | c0004 | t0002 | g0307 | EUR | TSI | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA20752 | hp2 | a0003 | c0003 | t0002 | g0208 | EUR | TSI | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA20805 | hp1 | a0002 | c0002 | t0014 | g0150 | EUR | TSI | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0087 | EUR | TSI | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA20905 | hp1 | a0002 | c0002 | t0003 | g0070 | SAS | GIH | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA20905 | hp2 | a0003 | c0003 | t0002 | g0158 | SAS | GIH | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01123 | hp1 | a0003 | c0003 | t0002 | g0115 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0289 | AMR | CLM | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02109 | hp1 | a0002 | c0002 | t0003 | g0091 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0323 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0290 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02486 | hp2 | a0002 | c0002 | t0004 | g0155 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG02559 | hp2 | a0002 | c0002 | t0004 | g0121 | AFR | ACB | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03471 | hp1 | a0003 | c0003 | t0002 | g0143 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0092 | AFR | MSL | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG06807 | hp1 | a0001 | c0005 | t0003 | g0228 | AFR | USA | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | USA | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA18955 | hp2 | a0003 | c0003 | t0002 | g0145 | EAS | JPT | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | USA | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA20300 | hp2 | a0004 | c0004 | t0009 | g0251 | AFR | USA | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA21309 | hp1 | a0003 | c0003 | t0002 | g0234 | AFR | LWK | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| NA21309 | hp2 | a0001 | c0005 | t0003 | g0231 | AFR | LWK | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0013 | g0272 | REF | REF | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| homoSapiens | grch38p0 | a0004 | c0004 | t0002 | g0199 | REF | REF | GFRAL_chr6_55322469_55407493 | GFRAL | chr6 | 55322469 | 55407493 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:55331777 | G | C | 1 | a0006 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.85G>C | p.Glu29Gln | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/9 | 171/1911 | 85/1185 | 29/394 | chr6 | 55331777 | |||
| chr6:55331789 | C | T | 2 | a0002 a0003 |
148 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(145): Show |
missense_variant | MODERATE | c.97C>T | p.Arg33Cys | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/9 | 183/1911 | 97/1185 | 33/394 | chr6 | 55331789 | |||
| chr6:55350097 | G | A | 1 | a0006 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.322G>A | p.Val108Met | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/9 | 408/1911 | 322/1185 | 108/394 | chr6 | 55350097 | |||
| chr6:55350134 | G | T | 1 | a0006 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.359G>T | p.Arg120Leu | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/9 | 445/1911 | 359/1185 | 120/394 | chr6 | 55350134 | |||
| chr6:55351396 | C | T | 1 | a0005 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.514C>T | p.Arg172Trp | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/9 | 600/1911 | 514/1185 | 172/394 | chr6 | 55351396 | |||
| chr6:55351546 | A | G | 1 | a0006 | 1 | HG02300.hp1 | missense_variant | MODERATE | c.664A>G | p.Ser222Gly | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/9 | 750/1911 | 664/1185 | 222/394 | chr6 | 55351546 | |||
| chr6:55401827 | T | C | 3 | a0001 a0002 a0006 |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
missense_variant | MODERATE | c.1159T>C | p.Ser387Pro | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 1245/1911 | 1159/1185 | 387/394 | chr6 | 55401827 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:55333898 | T | C | 1 | a0006c0006 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.270T>C | p.Tyr90Tyr | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/9 | 356/1911 | 270/1185 | 90/394 | chr6 | 55333898 | |||
| chr6:55359077 | A | G | 3 | a0001c0005 a0002c0010 a0004c0008 |
10 | HG01884.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
synonymous_variant | LOW | c.891A>G | p.Thr297Thr | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/9 | 977/1911 | 891/1185 | 297/394 | chr6 | 55359077 | |||
| chr6:55399415 | C | T | 1 | a0001c0007 | 1 | HG01952.hp2 | synonymous_variant | LOW | c.1095C>T | p.Ile365Ile | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/9 | 1181/1911 | 1095/1185 | 365/394 | chr6 | 55399415 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:55401924 | C | T | 19 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(16): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*71C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 71 | chr6 | 55401924 | ||||||
| chr6:55401998 | C | T | 4 | a0001c0001t0001 a0001c0001t0008 a0002c0002t0001 others(1): Show |
115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*145C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 145 | chr6 | 55401998 | ||||||
| chr6:55401999 | G | A | 1 | a0002c0002t0010 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 146 | chr6 | 55401999 | ||||||
| chr6:55402020 | A | G | 1 | a0002c0002t0007 | 2 | HG03942.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*167A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 167 | chr6 | 55402020 | ||||||
| chr6:55402069 | AAGGTTCA others(30): Show |
A | 1 | a0001c0001t0011 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*219_*255delGTTCAA others(31): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 219 | INFO_REALIGN_3_PRIME | chr6 | 55402069 | |||||
| chr6:55402097 | CT | C | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(15): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*246delT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 246 | INFO_REALIGN_3_PRIME | chr6 | 55402097 | |||||
| chr6:55402126 | C | T | 6 | a0001c0001t0004 a0001c0001t0012 a0001c0005t0004 others(3): Show |
75 | HG00323.hp1 HG00609.hp1 HG00738.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*273C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 273 | chr6 | 55402126 | ||||||
| chr6:55402135 | G | C | 1 | a0004c0004t0009 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*282G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 282 | chr6 | 55402135 | ||||||
| chr6:55402145 | T | A | 1 | a0002c0002t0014 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*292T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 292 | chr6 | 55402145 | ||||||
| chr6:55402146 | T | TTTTTTGT others(29): Show |
1 | a0004c0004t0005 | 3 | HG02258.hp1 HG02717.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*296_*331dupTTTGTA others(30): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 332 | INFO_REALIGN_3_PRIME | chr6 | 55402146 | |||||
| chr6:55402186 | G | T | 1 | a0001c0001t0008 | 2 | NA18986.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*333G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 333 | chr6 | 55402186 | ||||||
| chr6:55402187 | C | T | 2 | a0001c0001t0006 a0002c0002t0006 |
3 | HG02280.hp2 HG02723.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*334C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 334 | chr6 | 55402187 | ||||||
| chr6:55402323 | C | A | 19 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(16): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*470C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 470 | chr6 | 55402323 | ||||||
| chr6:55402432 | GA | G | 4 | a0001c0001t0001 a0001c0001t0008 a0002c0002t0001 others(1): Show |
115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*585delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 585 | INFO_REALIGN_3_PRIME | chr6 | 55402432 | |||||
| chr6:55402451 | T | C | 1 | a0001c0001t0012 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*598T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 9/9 | 598 | chr6 | 55402451 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:55327823 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.22+247T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55327823 | |||||||
| chr6:55327893 | C | T | 2 | a0002c0002t0003g0334 a0002c0002t0003g0335 |
2 | HG00438.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.22+317C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55327893 | |||||||
| chr6:55327914 | A | G | 1 | a0001c0001t0001g0333 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.22+338A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55327914 | |||||||
| chr6:55328031 | T | G | 2 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
2 | NA18939.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.22+455T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55328031 | |||||||
| chr6:55328093 | C | G | 1 | a0004c0004t0002g0332 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.22+517C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55328093 | |||||||
| chr6:55328152 | C | T | 1 | a0002c0002t0003g0331 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.22+576C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55328152 | |||||||
| chr6:55328223 | A | G | 1 | a0003c0003t0002g0330 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.22+647A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55328223 | |||||||
| chr6:55328440 | G | A | 1 | a0001c0001t0011g0040 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.22+864G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55328440 | |||||||
| chr6:55328480 | T | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0043 others(13): Show |
20 | HG00639.hp2 HG00738.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.22+904T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55328480 | |||||||
| chr6:55328483 | G | C | 48 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0086 others(45): Show |
53 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.22+907G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55328483 | |||||||
| chr6:55328812 | C | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | NA18954.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.22+1236C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55328812 | |||||||
| chr6:55328905 | G | A | 3 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | NA18953.hp2 NA19004.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.22+1329G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55328905 | |||||||
| chr6:55329041 | T | G | 1 | a0001c0001t0001g0102 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.22+1465T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55329041 | |||||||
| chr6:55329068 | T | C | 2 | a0003c0003t0002g0056 a0003c0003t0002g0057 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.22+1492T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55329068 | |||||||
| chr6:55329091 | C | A | 66 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(63): Show |
71 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.22+1515C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55329091 | |||||||
| chr6:55329187 | C | G | 1 | a0004c0004t0002g0332 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.22+1611C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55329187 | |||||||
| chr6:55329285 | CAAAAACT others(26): Show |
C | 1 | a0001c0001t0004g0164 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.22+1742_22+1774del others(33): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 55329285 | ||||||
| chr6:55329424 | T | C | 1 | a0003c0003t0002g0103 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.22+1848T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55329424 | |||||||
| chr6:55329570 | A | G | 7 | a0001c0001t0006g0329 a0001c0001t0011g0040 a0004c0004t0002g0035 others(4): Show |
8 | HG02451.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.22+1994A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55329570 | |||||||
| chr6:55329772 | C | G | 1 | a0001c0001t0001g0324 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.23-1943C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55329772 | |||||||
| chr6:55329811 | T | C | 1 | a0002c0002t0001g0058 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.23-1904T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55329811 | |||||||
| chr6:55329894 | T | G | 1 | a0004c0004t0002g0165 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.23-1821T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55329894 | |||||||
| chr6:55329922 | A | G | 51 | a0001c0001t0003g0322 a0001c0001t0003g0323 a0002c0002t0001g0058 others(48): Show |
56 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.23-1793A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55329922 | |||||||
| chr6:55329973 | T | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(59): Show |
79 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.23-1742T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55329973 | |||||||
| chr6:55330062 | A | G | 1 | a0002c0002t0003g0096 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.23-1653A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55330062 | |||||||
| chr6:55330098 | C | T | 80 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(77): Show |
96 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.23-1617C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55330098 | |||||||
| chr6:55330121 | C | T | 6 | a0002c0002t0003g0024 a0002c0002t0003g0254 a0002c0002t0003g0255 others(3): Show |
7 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-1594C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55330121 | |||||||
| chr6:55330370 | G | T | 6 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0004c0004t0002g0023 others(3): Show |
7 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-1345G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55330370 | |||||||
| chr6:55330570 | A | C | 1 | a0003c0003t0002g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.23-1145A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55330570 | |||||||
| chr6:55330582 | G | T | 6 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0004c0004t0002g0023 others(3): Show |
7 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-1133G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55330582 | |||||||
| chr6:55330605 | C | T | 1 | a0003c0003t0002g0162 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.23-1110C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55330605 | |||||||
| chr6:55330616 | C | A | 6 | a0002c0002t0003g0024 a0002c0002t0003g0254 a0002c0002t0003g0255 others(3): Show |
7 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.23-1099C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55330616 | |||||||
| chr6:55330657 | T | C | 1 | a0001c0001t0004g0257 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.23-1058T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55330657 | |||||||
| chr6:55330750 | C | T | 3 | a0003c0003t0002g0159 a0003c0003t0002g0160 a0003c0003t0002g0161 |
3 | HG00642.hp2 HG01516.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.23-965C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55330750 | |||||||
| chr6:55330868 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.23-847G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55330868 | |||||||
| chr6:55330990 | T | A | 1 | a0001c0001t0001g0166 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.23-725T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55330990 | |||||||
| chr6:55331023 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.23-692T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331023 | |||||||
| chr6:55331065 | C | T | 21 | a0002c0002t0003g0024 a0002c0002t0003g0236 a0002c0002t0003g0254 others(18): Show |
23 | HG02040.hp2 HG02145.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.23-650C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331065 | |||||||
| chr6:55331082 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.23-633C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331082 | |||||||
| chr6:55331147 | A | G | 107 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(104): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.23-568A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331147 | |||||||
| chr6:55331236 | C | T | 1 | a0001c0001t0004g0164 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.23-479C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331236 | |||||||
| chr6:55331241 | A | G | 67 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(64): Show |
72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.23-474A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331241 | |||||||
| chr6:55331262 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.23-453T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331262 | |||||||
| chr6:55331316 | G | T | 107 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(104): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.23-399G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331316 | |||||||
| chr6:55331322 | G | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.23-393G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331322 | |||||||
| chr6:55331366 | G | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.23-349G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331366 | |||||||
| chr6:55331377 | G | A | 107 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(104): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.23-338G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331377 | |||||||
| chr6:55331404 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.23-311T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331404 | |||||||
| chr6:55331465 | A | T | 107 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(104): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.23-250A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331465 | |||||||
| chr6:55331501 | C | A | 260 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(257): Show |
293 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.23-214C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331501 | |||||||
| chr6:55331502 | G | A | 1 | a0001c0001t0003g0018 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.23-213G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331502 | |||||||
| chr6:55331516 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.23-199A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331516 | |||||||
| chr6:55331575 | G | A | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.23-140G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 1/8 | chr6 | 55331575 | |||||||
| chr6:55331941 | T | A | 4 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0212 others(1): Show |
4 | HG02559.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.157+92T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55331941 | |||||||
| chr6:55332043 | C | A | 6 | a0002c0002t0003g0024 a0002c0002t0003g0254 a0002c0002t0003g0255 others(3): Show |
7 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.157+194C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332043 | |||||||
| chr6:55332127 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.157+278A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332127 | |||||||
| chr6:55332148 | C | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.157+299C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332148 | |||||||
| chr6:55332149 | T | C | 5 | a0004c0004t0002g0035 a0004c0004t0002g0325 a0004c0004t0002g0326 others(2): Show |
6 | HG02451.hp1 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.157+300T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332149 | |||||||
| chr6:55332152 | T | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(58): Show |
78 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.157+303T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332152 | |||||||
| chr6:55332281 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.157+432G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332281 | |||||||
| chr6:55332339 | G | A | 2 | a0004c0004t0002g0023 a0004c0004t0002g0249 |
3 | HG01358.hp1 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.157+490G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332339 | |||||||
| chr6:55332416 | T | G | 3 | a0002c0002t0003g0010 a0002c0002t0003g0059 a0002c0002t0003g0060 |
4 | NA18941.hp1 NA19064.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.157+567T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332416 | |||||||
| chr6:55332501 | C | G | 46 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0086 others(43): Show |
51 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.157+652C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332501 | |||||||
| chr6:55332544 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.157+695C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332544 | |||||||
| chr6:55332568 | C | T | 11 | a0002c0002t0003g0236 a0003c0003t0002g0237 a0003c0003t0002g0238 others(8): Show |
11 | HG02040.hp2 HG02523.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.157+719C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332568 | |||||||
| chr6:55332697 | C | G | 48 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0086 others(45): Show |
53 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.157+848C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332697 | |||||||
| chr6:55332704 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.157+855G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332704 | |||||||
| chr6:55332714 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.157+865G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332714 | |||||||
| chr6:55332724 | T | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.157+875T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55332724 | |||||||
| chr6:55332900 | CAT | C | 6 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(3): Show |
6 | HG00099.hp2 HG01255.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-884_158-883del others(2): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 55332900 | ||||||
| chr6:55333032 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.158-754G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55333032 | |||||||
| chr6:55333171 | C | T | 67 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(64): Show |
72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.158-615C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55333171 | |||||||
| chr6:55333195 | A | G | 9 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0004g0164 others(6): Show |
10 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.158-591A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55333195 | |||||||
| chr6:55333259 | A | T | 6 | a0002c0002t0003g0024 a0002c0002t0003g0254 a0002c0002t0003g0255 others(3): Show |
7 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.158-527A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55333259 | |||||||
| chr6:55333311 | A | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(104): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.158-475A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55333311 | |||||||
| chr6:55333588 | A | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(62): Show |
82 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.158-198A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55333588 | |||||||
| chr6:55333678 | A | G | 1 | a0003c0003t0002g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.158-108A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 2/8 | chr6 | 55333678 | |||||||
| chr6:55334039 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+95G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55334039 | |||||||
| chr6:55334115 | G | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(61): Show |
81 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.316+171G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55334115 | |||||||
| chr6:55334189 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+245C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55334189 | |||||||
| chr6:55334207 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+263A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55334207 | |||||||
| chr6:55334319 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+375G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55334319 | |||||||
| chr6:55334510 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+566G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55334510 | |||||||
| chr6:55334653 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+709G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55334653 | |||||||
| chr6:55334690 | GTCCAA | G | 259 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.316+752_316+756del others(5): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55334690 | ||||||
| chr6:55334745 | C | T | 14 | a0002c0002t0003g0236 a0002c0010t0003g0235 a0003c0003t0002g0022 others(11): Show |
15 | HG02040.hp2 HG02523.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.316+801C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55334745 | |||||||
| chr6:55334960 | T | G | 7 | a0001c0001t0001g0259 a0001c0001t0004g0025 a0001c0001t0004g0260 others(4): Show |
8 | HG02027.hp1 HG03831.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+1016T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55334960 | |||||||
| chr6:55335088 | A | C | 1 | a0002c0002t0004g0157 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.316+1144A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335088 | |||||||
| chr6:55335241 | A | G | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(321): Show |
374 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.316+1297A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335241 | |||||||
| chr6:55335293 | G | C | 259 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.316+1349G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335293 | |||||||
| chr6:55335353 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+1409C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335353 | |||||||
| chr6:55335452 | G | C | 19 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(16): Show |
21 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.316+1508G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335452 | |||||||
| chr6:55335461 | A | T | 4 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0212 others(1): Show |
4 | HG02559.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+1517A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335461 | |||||||
| chr6:55335558 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+1614T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335558 | |||||||
| chr6:55335570 | A | T | 1 | a0003c0003t0002g0233 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.316+1626A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335570 | |||||||
| chr6:55335592 | T | C | 67 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(64): Show |
72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.316+1648T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335592 | |||||||
| chr6:55335603 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+1659A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335603 | |||||||
| chr6:55335664 | G | T | 1 | a0001c0001t0003g0018 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.316+1720G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335664 | |||||||
| chr6:55335675 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.316+1731A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335675 | |||||||
| chr6:55335727 | G | A | 1 | a0003c0003t0002g0022 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.316+1783G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335727 | |||||||
| chr6:55335895 | C | CTTTAT | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(118): Show |
145 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.316+1990_316+1994d others(7): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55335895 | ||||||
| chr6:55335895 | C | CTTTATTT others(3): Show |
36 | a0001c0001t0001g0167 a0002c0002t0001g0122 a0002c0002t0003g0120 others(33): Show |
38 | HG00558.hp2 HG00621.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.316+1985_316+1994d others(12): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55335895 | ||||||
| chr6:55335895 | C | CTTTATTT others(8): Show |
14 | a0001c0001t0003g0205 a0001c0001t0003g0207 a0002c0002t0001g0109 others(11): Show |
15 | HG01069.hp2 HG01243.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.316+1980_316+1994d others(17): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55335895 | ||||||
| chr6:55335895 | C | CTTTATTT others(13): Show |
4 | a0002c0002t0001g0108 a0002c0002t0004g0106 a0002c0002t0004g0107 others(1): Show |
4 | HG01070.hp1 HG01346.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+1975_316+1994d others(22): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55335895 | ||||||
| chr6:55335895 | C | CTTTATTT others(18): Show |
1 | a0002c0002t0001g0104 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.316+1970_316+1994d others(27): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55335895 | ||||||
| chr6:55335895 | CTTTAT | C | 14 | a0001c0001t0003g0018 a0001c0001t0003g0322 a0001c0001t0003g0323 others(11): Show |
16 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.316+1990_316+1994d others(7): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55335895 | ||||||
| chr6:55335895 | CTTTATTT others(3): Show |
C | 8 | a0002c0002t0003g0024 a0002c0002t0003g0254 a0002c0002t0003g0255 others(5): Show |
9 | HG02040.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.316+1985_316+1994d others(12): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55335895 | ||||||
| chr6:55335895 | CTTTATTT others(8): Show |
C | 106 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(103): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.316+1980_316+1994d others(17): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55335895 | ||||||
| chr6:55335895 | CTTTATTT others(13): Show |
C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+1975_316+1994d others(22): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55335895 | ||||||
| chr6:55335904 | ATTTTATT others(6): Show |
A | 9 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0004g0164 others(6): Show |
10 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.316+1962_316+1974d others(15): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55335904 | ||||||
| chr6:55335967 | C | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+2023C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335967 | |||||||
| chr6:55335991 | C | G | 2 | a0002c0002t0003g0139 a0002c0002t0003g0331 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.316+2047C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55335991 | |||||||
| chr6:55336032 | C | T | 27 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(24): Show |
30 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.316+2088C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336032 | |||||||
| chr6:55336047 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+2103T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336047 | |||||||
| chr6:55336104 | C | A | 1 | a0001c0001t0001g0166 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.316+2160C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336104 | |||||||
| chr6:55336106 | G | T | 1 | a0003c0003t0002g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.316+2162G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336106 | |||||||
| chr6:55336147 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+2203T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336147 | |||||||
| chr6:55336163 | G | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+2219G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336163 | |||||||
| chr6:55336229 | C | G | 1 | a0001c0001t0003g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.316+2285C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336229 | |||||||
| chr6:55336319 | G | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+2375G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336319 | |||||||
| chr6:55336389 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+2445T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336389 | |||||||
| chr6:55336703 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+2759T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336703 | |||||||
| chr6:55336799 | T | G | 5 | a0004c0004t0002g0035 a0004c0004t0002g0325 a0004c0004t0002g0326 others(2): Show |
6 | HG02451.hp1 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.316+2855T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336799 | |||||||
| chr6:55336961 | A | T | 259 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.316+3017A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336961 | |||||||
| chr6:55336983 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+3039T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55336983 | |||||||
| chr6:55337130 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+3186T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337130 | |||||||
| chr6:55337132 | C | T | 1 | a0001c0007t0004g0320 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.316+3188C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337132 | |||||||
| chr6:55337165 | G | A | 1 | a0001c0001t0004g0164 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.316+3221G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337165 | |||||||
| chr6:55337165 | G | T | 1 | a0003c0003t0002g0246 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.316+3221G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337165 | |||||||
| chr6:55337214 | G | A | 1 | a0003c0003t0002g0140 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.316+3270G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337214 | |||||||
| chr6:55337237 | C | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+3293C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337237 | |||||||
| chr6:55337270 | T | A | 7 | a0002c0002t0003g0024 a0002c0002t0003g0254 a0002c0002t0003g0255 others(4): Show |
8 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+3326T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337270 | |||||||
| chr6:55337372 | GTTTTCTT others(4): Show |
G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(62): Show |
82 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.316+3430_316+3440d others(13): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55337372 | ||||||
| chr6:55337401 | C | T | 67 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(64): Show |
72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.316+3457C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337401 | |||||||
| chr6:55337405 | G | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+3461G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337405 | |||||||
| chr6:55337551 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+3607A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337551 | |||||||
| chr6:55337572 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.316+3628G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337572 | |||||||
| chr6:55337598 | T | C | 1 | a0003c0003t0002g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.316+3654T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337598 | |||||||
| chr6:55337648 | G | T | 9 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0004g0164 others(6): Show |
10 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.316+3704G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337648 | |||||||
| chr6:55337753 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+3809T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337753 | |||||||
| chr6:55337758 | A | G | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(321): Show |
374 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.316+3814A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337758 | |||||||
| chr6:55337812 | T | A | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.316+3868T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337812 | |||||||
| chr6:55337893 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+3949T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337893 | |||||||
| chr6:55337923 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+3979G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337923 | |||||||
| chr6:55337963 | C | T | 1 | a0001c0001t0004g0319 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.316+4019C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55337963 | |||||||
| chr6:55338056 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+4112T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338056 | |||||||
| chr6:55338070 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+4126A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338070 | |||||||
| chr6:55338130 | G | A | 49 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0086 others(46): Show |
54 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.316+4186G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338130 | |||||||
| chr6:55338166 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+4222C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338166 | |||||||
| chr6:55338167 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+4223T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338167 | |||||||
| chr6:55338176 | C | T | 67 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(64): Show |
72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.316+4232C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338176 | |||||||
| chr6:55338205 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+4261C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338205 | |||||||
| chr6:55338221 | C | G | 106 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(103): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.316+4277C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338221 | |||||||
| chr6:55338324 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.316+4380A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338324 | |||||||
| chr6:55338342 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+4398A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338342 | |||||||
| chr6:55338373 | A | G | 1 | a0003c0003t0002g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.316+4429A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338373 | |||||||
| chr6:55338381 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+4437T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338381 | |||||||
| chr6:55338385 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+4441G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338385 | |||||||
| chr6:55338468 | T | C | 79 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(76): Show |
95 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.316+4524T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338468 | |||||||
| chr6:55338553 | G | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+4609G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338553 | |||||||
| chr6:55338554 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+4610T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338554 | |||||||
| chr6:55338571 | G | C | 106 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(103): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.316+4627G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338571 | |||||||
| chr6:55338577 | C | T | 2 | a0004c0004t0002g0023 a0004c0004t0002g0249 |
3 | HG01358.hp1 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.316+4633C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338577 | |||||||
| chr6:55338581 | T | G | 3 | a0003c0003t0002g0012 a0003c0003t0002g0116 a0003c0003t0002g0117 |
4 | HG02258.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+4637T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338581 | |||||||
| chr6:55338603 | G | C | 67 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(64): Show |
72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.316+4659G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338603 | |||||||
| chr6:55338642 | T | C | 2 | a0001c0001t0004g0265 a0001c0001t0004g0266 |
2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.316+4698T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338642 | |||||||
| chr6:55338712 | A | T | 259 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.316+4768A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338712 | |||||||
| chr6:55338815 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+4871A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338815 | |||||||
| chr6:55338944 | T | A | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(321): Show |
374 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.316+5000T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338944 | |||||||
| chr6:55338969 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+5025G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338969 | |||||||
| chr6:55338983 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+5039C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55338983 | |||||||
| chr6:55339007 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+5063A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339007 | |||||||
| chr6:55339070 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(62): Show |
82 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.316+5126G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339070 | |||||||
| chr6:55339129 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+5185G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339129 | |||||||
| chr6:55339174 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0192 |
4 | NA18952.hp1 NA18955.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+5230C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339174 | |||||||
| chr6:55339209 | T | C | 1 | a0001c0001t0008g0169 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.316+5265T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339209 | |||||||
| chr6:55339219 | T | C | 106 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(103): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.316+5275T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339219 | |||||||
| chr6:55339256 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.316+5312C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339256 | |||||||
| chr6:55339345 | T | C | 14 | a0002c0002t0003g0236 a0002c0010t0003g0235 a0003c0003t0002g0022 others(11): Show |
15 | HG02040.hp2 HG02523.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.316+5401T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339345 | |||||||
| chr6:55339353 | G | T | 2 | a0003c0003t0002g0137 a0003c0003t0002g0138 |
2 | HG00741.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.316+5409G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339353 | |||||||
| chr6:55339453 | G | T | 8 | a0001c0005t0003g0226 a0001c0005t0003g0228 a0001c0005t0003g0229 others(5): Show |
9 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.316+5509G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339453 | |||||||
| chr6:55339499 | A | G | 6 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0004c0004t0002g0023 others(3): Show |
7 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.316+5555A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339499 | |||||||
| chr6:55339512 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+5568G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339512 | |||||||
| chr6:55339549 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+5605T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339549 | |||||||
| chr6:55339676 | A | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+5732A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339676 | |||||||
| chr6:55339710 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+5766A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339710 | |||||||
| chr6:55339811 | T | G | 1 | a0002c0002t0004g0118 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.316+5867T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55339811 | |||||||
| chr6:55340000 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+6056G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340000 | |||||||
| chr6:55340023 | A | T | 7 | a0002c0002t0003g0024 a0002c0002t0003g0254 a0002c0002t0003g0255 others(4): Show |
8 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+6079A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340023 | |||||||
| chr6:55340036 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+6092A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340036 | |||||||
| chr6:55340050 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.316+6106C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340050 | |||||||
| chr6:55340051 | G | A | 14 | a0002c0002t0003g0236 a0002c0010t0003g0235 a0003c0003t0002g0022 others(11): Show |
15 | HG02040.hp2 HG02523.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.316+6107G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340051 | |||||||
| chr6:55340122 | A | G | 7 | a0002c0002t0003g0024 a0002c0002t0003g0254 a0002c0002t0003g0255 others(4): Show |
8 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+6178A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340122 | |||||||
| chr6:55340135 | A | G | 67 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(64): Show |
72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.316+6191A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340135 | |||||||
| chr6:55340189 | C | G | 14 | a0002c0002t0003g0236 a0002c0010t0003g0235 a0003c0003t0002g0022 others(11): Show |
15 | HG02040.hp2 HG02523.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.316+6245C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340189 | |||||||
| chr6:55340223 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+6279G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340223 | |||||||
| chr6:55340305 | G | A | 1 | a0003c0003t0002g0141 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.316+6361G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340305 | |||||||
| chr6:55340348 | A | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(104): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.316+6404A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340348 | |||||||
| chr6:55340363 | G | A | 7 | a0002c0002t0003g0024 a0002c0002t0003g0254 a0002c0002t0003g0255 others(4): Show |
8 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+6419G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340363 | |||||||
| chr6:55340373 | G | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+6429G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340373 | |||||||
| chr6:55340412 | C | T | 259 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.316+6468C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340412 | |||||||
| chr6:55340415 | A | G | 1 | a0001c0001t0004g0318 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.316+6471A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340415 | |||||||
| chr6:55340449 | C | A | 259 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.316+6505C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340449 | |||||||
| chr6:55340554 | T | C | 2 | a0002c0002t0010g0105 a0003c0003t0002g0142 |
2 | HG00639.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.316+6610T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340554 | |||||||
| chr6:55340558 | A | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+6614A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340558 | |||||||
| chr6:55340582 | A | G | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.316+6638A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340582 | |||||||
| chr6:55340592 | C | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+6648C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340592 | |||||||
| chr6:55340609 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(62): Show |
82 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.316+6665C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340609 | |||||||
| chr6:55340641 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+6697A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340641 | |||||||
| chr6:55340642 | G | A | 46 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0086 others(43): Show |
51 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.316+6698G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340642 | |||||||
| chr6:55340652 | A | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+6708A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340652 | |||||||
| chr6:55340676 | G | T | 1 | a0001c0001t0003g0018 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.316+6732G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340676 | |||||||
| chr6:55340704 | G | A | 107 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(104): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.316+6760G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340704 | |||||||
| chr6:55340748 | A | G | 1 | a0004c0004t0002g0317 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.316+6804A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340748 | |||||||
| chr6:55340790 | C | T | 3 | a0002c0002t0003g0334 a0002c0002t0003g0335 a0006c0006t0003g0258 |
3 | HG00438.hp2 HG02132.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.316+6846C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340790 | |||||||
| chr6:55340823 | C | A | 1 | a0004c0004t0002g0332 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.316+6879C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340823 | |||||||
| chr6:55340834 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+6890A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340834 | |||||||
| chr6:55340877 | T | G | 136 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0086 others(133): Show |
148 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.316+6933T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340877 | |||||||
| chr6:55340881 | G | A | 106 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(103): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.316+6937G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340881 | |||||||
| chr6:55340964 | C | T | 67 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(64): Show |
72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.316+7020C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55340964 | |||||||
| chr6:55341007 | G | A | 14 | a0002c0002t0003g0236 a0002c0010t0003g0235 a0003c0003t0002g0022 others(11): Show |
15 | HG02040.hp2 HG02523.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.316+7063G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341007 | |||||||
| chr6:55341013 | C | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(62): Show |
82 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.316+7069C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341013 | |||||||
| chr6:55341049 | T | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(104): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.316+7105T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341049 | |||||||
| chr6:55341084 | T | C | 46 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0086 others(43): Show |
51 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.316+7140T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341084 | |||||||
| chr6:55341094 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7150T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341094 | |||||||
| chr6:55341184 | G | A | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.316+7240G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341184 | |||||||
| chr6:55341184 | G | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7240G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341184 | |||||||
| chr6:55341191 | A | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7247A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341191 | |||||||
| chr6:55341210 | T | G | 136 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0086 others(133): Show |
148 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.316+7266T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341210 | |||||||
| chr6:55341284 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7340G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341284 | |||||||
| chr6:55341314 | G | C | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(321): Show |
374 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(371): Show |
intron_variant | MODIFIER | c.316+7370G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341314 | |||||||
| chr6:55341320 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7376C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341320 | |||||||
| chr6:55341337 | C | A | 1 | a0003c0003t0002g0233 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.316+7393C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341337 | |||||||
| chr6:55341338 | G | A | 4 | a0003c0003t0002g0114 a0003c0003t0002g0119 a0003c0003t0002g0233 others(1): Show |
4 | HG00621.hp1 HG00673.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+7394G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341338 | |||||||
| chr6:55341382 | C | T | 2 | a0004c0004t0002g0023 a0004c0004t0002g0249 |
3 | HG01358.hp1 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.316+7438C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341382 | |||||||
| chr6:55341389 | T | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(104): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.316+7445T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341389 | |||||||
| chr6:55341393 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7449T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341393 | |||||||
| chr6:55341398 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7454C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341398 | |||||||
| chr6:55341473 | G | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7529G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341473 | |||||||
| chr6:55341582 | G | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7638G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341582 | |||||||
| chr6:55341592 | T | A | 1 | a0001c0001t0004g0026 | 2 | HG02074.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.316+7648T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341592 | |||||||
| chr6:55341641 | A | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7697A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341641 | |||||||
| chr6:55341646 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7702G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341646 | |||||||
| chr6:55341654 | T | C | 2 | a0004c0004t0009g0251 a0005c0009t0002g0250 |
2 | HG02055.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.316+7710T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341654 | |||||||
| chr6:55341685 | C | T | 68 | a0001c0001t0001g0191 a0002c0002t0001g0104 a0002c0002t0001g0108 others(65): Show |
73 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.316+7741C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341685 | |||||||
| chr6:55341702 | G | A | 3 | a0001c0001t0004g0267 a0001c0001t0004g0268 a0001c0001t0004g0269 |
3 | NA18978.hp1 NA19005.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.316+7758G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341702 | |||||||
| chr6:55341731 | A | C | 7 | a0001c0001t0006g0329 a0001c0001t0011g0040 a0004c0004t0002g0035 others(4): Show |
8 | HG02451.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+7787A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341731 | |||||||
| chr6:55341738 | A | T | 1 | a0001c0001t0001g0098 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.316+7794A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341738 | |||||||
| chr6:55341739 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7795T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341739 | |||||||
| chr6:55341743 | C | T | 67 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(64): Show |
72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.316+7799C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341743 | |||||||
| chr6:55341822 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7878C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341822 | |||||||
| chr6:55341849 | C | A | 2 | a0001c0005t0003g0226 a0004c0008t0002g0227 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.316+7905C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341849 | |||||||
| chr6:55341866 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7922C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341866 | |||||||
| chr6:55341867 | A | G | 47 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0086 others(44): Show |
52 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.316+7923A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341867 | |||||||
| chr6:55341898 | C | T | 9 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0004g0164 others(6): Show |
10 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.316+7954C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341898 | |||||||
| chr6:55341915 | G | A | 3 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0005c0009t0002g0250 |
3 | HG01891.hp2 HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.316+7971G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341915 | |||||||
| chr6:55341916 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+7972A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341916 | |||||||
| chr6:55341943 | TGAAAG | T | 5 | a0004c0004t0002g0035 a0004c0004t0002g0325 a0004c0004t0002g0326 others(2): Show |
6 | HG02451.hp1 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.316+8003_316+8007d others(7): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55341943 | ||||||
| chr6:55341944 | G | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+8000G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341944 | |||||||
| chr6:55341953 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.316+8009C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55341953 | |||||||
| chr6:55342051 | G | A | 2 | a0003c0003t0002g0056 a0003c0003t0002g0057 |
2 | HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.317-8041G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342051 | |||||||
| chr6:55342096 | C | G | 8 | a0001c0001t0003g0018 a0001c0001t0003g0322 a0001c0001t0003g0323 others(5): Show |
9 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.317-7996C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342096 | |||||||
| chr6:55342103 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7989G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342103 | |||||||
| chr6:55342108 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.317-7984C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342108 | |||||||
| chr6:55342286 | T | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7806T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342286 | |||||||
| chr6:55342297 | G | A | 1 | a0001c0001t0006g0219 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.317-7795G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342297 | |||||||
| chr6:55342300 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7792G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342300 | |||||||
| chr6:55342319 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7773A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342319 | |||||||
| chr6:55342328 | G | A | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.317-7764G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342328 | |||||||
| chr6:55342369 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7723T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342369 | |||||||
| chr6:55342383 | G | T | 1 | a0002c0002t0004g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.317-7709G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342383 | |||||||
| chr6:55342398 | A | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(104): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.317-7694A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342398 | |||||||
| chr6:55342453 | A | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7639A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342453 | |||||||
| chr6:55342463 | A | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7629A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342463 | |||||||
| chr6:55342506 | A | C | 98 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(95): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.317-7586A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342506 | |||||||
| chr6:55342525 | C | A | 2 | a0003c0003t0002g0137 a0003c0003t0002g0138 |
2 | HG00741.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.317-7567C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342525 | |||||||
| chr6:55342543 | A | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7549A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342543 | |||||||
| chr6:55342548 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.317-7544C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342548 | |||||||
| chr6:55342549 | G | A | 7 | a0002c0002t0003g0024 a0002c0002t0003g0254 a0002c0002t0003g0255 others(4): Show |
8 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.317-7543G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342549 | |||||||
| chr6:55342569 | C | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7523C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342569 | |||||||
| chr6:55342594 | G | A | 106 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(103): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.317-7498G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342594 | |||||||
| chr6:55342596 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7496T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342596 | |||||||
| chr6:55342597 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7495G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342597 | |||||||
| chr6:55342598 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7494T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342598 | |||||||
| chr6:55342619 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7473C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342619 | |||||||
| chr6:55342642 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.317-7450C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342642 | |||||||
| chr6:55342684 | C | T | 106 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(103): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.317-7408C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342684 | |||||||
| chr6:55342820 | G | A | 8 | a0001c0005t0003g0226 a0001c0005t0003g0228 a0001c0005t0003g0229 others(5): Show |
9 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.317-7272G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342820 | |||||||
| chr6:55342833 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7259T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342833 | |||||||
| chr6:55342853 | C | G | 1 | a0001c0001t0001g0189 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.317-7239C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342853 | |||||||
| chr6:55342896 | A | G | 1 | a0003c0003t0002g0136 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.317-7196A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342896 | |||||||
| chr6:55342904 | A | C | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.317-7188A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342904 | |||||||
| chr6:55342912 | G | A | 1 | a0001c0001t0003g0220 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.317-7180G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342912 | |||||||
| chr6:55342924 | G | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7168G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342924 | |||||||
| chr6:55342961 | G | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7131G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342961 | |||||||
| chr6:55342970 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-7122G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55342970 | |||||||
| chr6:55343126 | G | C | 106 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(103): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.317-6966G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343126 | |||||||
| chr6:55343143 | C | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-6949C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343143 | |||||||
| chr6:55343206 | G | C | 3 | a0001c0001t0006g0329 a0001c0001t0011g0040 a0006c0006t0003g0258 |
3 | HG02300.hp1 HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.317-6886G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343206 | |||||||
| chr6:55343233 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-6859A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343233 | |||||||
| chr6:55343259 | T | C | 1 | a0002c0002t0003g0011 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.317-6833T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343259 | |||||||
| chr6:55343264 | C | T | 14 | a0002c0002t0003g0236 a0002c0010t0003g0235 a0003c0003t0002g0022 others(11): Show |
15 | HG02040.hp2 HG02523.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.317-6828C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343264 | |||||||
| chr6:55343271 | T | C | 14 | a0002c0002t0003g0236 a0002c0010t0003g0235 a0003c0003t0002g0022 others(11): Show |
15 | HG02040.hp2 HG02523.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.317-6821T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343271 | |||||||
| chr6:55343309 | C | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-6783C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343309 | |||||||
| chr6:55343324 | T | G | 2 | a0002c0002t0003g0065 a0003c0003t0002g0066 |
2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.317-6768T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343324 | |||||||
| chr6:55343384 | C | A | 1 | a0001c0001t0003g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.317-6708C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343384 | |||||||
| chr6:55343385 | G | A | 136 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0086 others(133): Show |
148 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.317-6707G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343385 | |||||||
| chr6:55343410 | C | A | 7 | a0001c0001t0006g0329 a0001c0001t0011g0040 a0004c0004t0002g0035 others(4): Show |
8 | HG02451.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.317-6682C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343410 | |||||||
| chr6:55343417 | G | C | 2 | a0001c0001t0003g0205 a0004c0004t0002g0206 |
2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.317-6675G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343417 | |||||||
| chr6:55343470 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-6622T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343470 | |||||||
| chr6:55343490 | T | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-6602T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343490 | |||||||
| chr6:55343710 | A | C | 106 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(103): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.317-6382A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343710 | |||||||
| chr6:55343713 | C | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-6379C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343713 | |||||||
| chr6:55343748 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-6344T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343748 | |||||||
| chr6:55343850 | C | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(58): Show |
78 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.317-6242C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343850 | |||||||
| chr6:55343943 | G | T | 48 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0086 others(45): Show |
53 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.317-6149G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343943 | |||||||
| chr6:55343989 | A | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-6103A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55343989 | |||||||
| chr6:55344011 | C | A | 1 | a0004c0004t0002g0317 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.317-6081C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344011 | |||||||
| chr6:55344032 | A | T | 67 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0109 others(64): Show |
72 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.317-6060A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344032 | |||||||
| chr6:55344145 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-5947T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344145 | |||||||
| chr6:55344202 | A | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-5890A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344202 | |||||||
| chr6:55344289 | A | G | 2 | a0001c0001t0003g0205 a0004c0004t0002g0206 |
2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.317-5803A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344289 | |||||||
| chr6:55344389 | C | T | 2 | a0004c0004t0005g0203 a0004c0004t0005g0204 |
2 | HG02258.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.317-5703C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344389 | |||||||
| chr6:55344485 | A | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-5607A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344485 | |||||||
| chr6:55344492 | G | A | 1 | a0003c0003t0002g0114 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.317-5600G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344492 | |||||||
| chr6:55344531 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-5561G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344531 | |||||||
| chr6:55344574 | A | G | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.317-5518A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344574 | |||||||
| chr6:55344590 | G | A | 3 | a0002c0002t0003g0334 a0002c0002t0003g0335 a0006c0006t0003g0258 |
3 | HG00438.hp2 HG02132.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.317-5502G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344590 | |||||||
| chr6:55344692 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0003g0193 |
2 | HG06807.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.317-5400G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344692 | |||||||
| chr6:55344722 | A | T | 1 | a0002c0002t0003g0096 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.317-5370A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344722 | |||||||
| chr6:55344740 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-5352A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344740 | |||||||
| chr6:55344757 | G | C | 2 | a0002c0002t0003g0067 a0002c0002t0003g0096 |
2 | NA18966.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.317-5335G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344757 | |||||||
| chr6:55344774 | C | T | 1 | a0001c0001t0003g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.317-5318C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344774 | |||||||
| chr6:55344793 | C | T | 2 | a0003c0003t0002g0243 a0003c0003t0002g0244 |
2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.317-5299C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344793 | |||||||
| chr6:55344797 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-5295A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344797 | |||||||
| chr6:55344865 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0270 a0001c0001t0001g0271 |
5 | HG00099.hp1 HG01070.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-5227G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344865 | |||||||
| chr6:55344866 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-5226C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344866 | |||||||
| chr6:55344877 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0188 |
4 | HG00621.hp2 NA18942.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-5215A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344877 | |||||||
| chr6:55344939 | C | A | 1 | a0001c0001t0001g0171 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.317-5153C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344939 | |||||||
| chr6:55344965 | T | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(104): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.317-5127T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55344965 | |||||||
| chr6:55345011 | A | T | 1 | a0002c0002t0003g0093 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.317-5081A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345011 | |||||||
| chr6:55345092 | A | G | 9 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0004g0164 others(6): Show |
10 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.317-5000A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345092 | |||||||
| chr6:55345168 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.317-4924C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345168 | |||||||
| chr6:55345207 | T | C | 5 | a0004c0004t0002g0035 a0004c0004t0002g0325 a0004c0004t0002g0326 others(2): Show |
6 | HG02451.hp1 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-4885T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345207 | |||||||
| chr6:55345226 | G | A | 5 | a0001c0005t0003g0228 a0001c0005t0003g0229 a0001c0005t0003g0230 others(2): Show |
6 | HG02896.hp1 HG02897.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-4866G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345226 | |||||||
| chr6:55345274 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-4818T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345274 | |||||||
| chr6:55345306 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-4786G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345306 | |||||||
| chr6:55345318 | A | C | 7 | a0001c0001t0006g0329 a0001c0001t0011g0040 a0004c0004t0002g0035 others(4): Show |
8 | HG02451.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.317-4774A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345318 | |||||||
| chr6:55345342 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-4750A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345342 | |||||||
| chr6:55345455 | G | A | 107 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(104): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.317-4637G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345455 | |||||||
| chr6:55345495 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-4597G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345495 | |||||||
| chr6:55345513 | T | C | 259 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.317-4579T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345513 | |||||||
| chr6:55345565 | A | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-4527A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345565 | |||||||
| chr6:55345567 | G | T | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.317-4525G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345567 | |||||||
| chr6:55345577 | C | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-4515C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345577 | |||||||
| chr6:55345627 | G | T | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.317-4465G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345627 | |||||||
| chr6:55345631 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-4461C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345631 | |||||||
| chr6:55345635 | C | A | 2 | a0001c0001t0006g0329 a0001c0001t0011g0040 |
2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.317-4457C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345635 | |||||||
| chr6:55345682 | A | T | 2 | a0001c0001t0006g0329 a0001c0001t0011g0040 |
2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.317-4410A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345682 | |||||||
| chr6:55345722 | T | C | 174 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(171): Show |
198 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.317-4370T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345722 | |||||||
| chr6:55345737 | T | C | 3 | a0002c0002t0003g0120 a0002c0002t0004g0121 a0002c0002t0004g0157 |
3 | HG01891.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.317-4355T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345737 | |||||||
| chr6:55345806 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-4286G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345806 | |||||||
| chr6:55345926 | T | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-4166T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345926 | |||||||
| chr6:55345943 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(59): Show |
79 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.317-4149C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345943 | |||||||
| chr6:55345948 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-4144T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55345948 | |||||||
| chr6:55346068 | T | C | 1 | a0002c0002t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.317-4024T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346068 | |||||||
| chr6:55346093 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3999G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346093 | |||||||
| chr6:55346111 | G | A | 2 | a0002c0002t0001g0109 a0002c0002t0001g0122 |
2 | HG01361.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.317-3981G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346111 | |||||||
| chr6:55346175 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3917A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346175 | |||||||
| chr6:55346214 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3878T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346214 | |||||||
| chr6:55346262 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3830T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346262 | |||||||
| chr6:55346291 | C | A | 8 | a0001c0005t0003g0226 a0001c0005t0003g0228 a0001c0005t0003g0229 others(5): Show |
9 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.317-3801C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346291 | |||||||
| chr6:55346348 | A | T | 14 | a0002c0002t0003g0236 a0002c0010t0003g0235 a0003c0003t0002g0022 others(11): Show |
15 | HG02040.hp2 HG02523.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.317-3744A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346348 | |||||||
| chr6:55346395 | C | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3697C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346395 | |||||||
| chr6:55346432 | A | G | 1 | a0002c0002t0001g0058 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.317-3660A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346432 | |||||||
| chr6:55346439 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3653A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346439 | |||||||
| chr6:55346441 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3651A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346441 | |||||||
| chr6:55346450 | C | A | 8 | a0001c0001t0003g0018 a0001c0001t0003g0322 a0001c0001t0003g0323 others(5): Show |
9 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.317-3642C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346450 | |||||||
| chr6:55346473 | A | G | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.317-3619A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346473 | |||||||
| chr6:55346530 | C | T | 2 | a0001c0001t0006g0329 a0001c0001t0011g0040 |
2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.317-3562C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346530 | |||||||
| chr6:55346600 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3492G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346600 | |||||||
| chr6:55346627 | C | T | 2 | a0001c0001t0006g0329 a0001c0001t0011g0040 |
2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.317-3465C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346627 | |||||||
| chr6:55346630 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3462A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346630 | |||||||
| chr6:55346656 | C | T | 3 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0113 |
3 | HG03491.hp2 HG03492.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.317-3436C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346656 | |||||||
| chr6:55346673 | C | T | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.317-3419C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346673 | |||||||
| chr6:55346713 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3379A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346713 | |||||||
| chr6:55346725 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3367G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346725 | |||||||
| chr6:55346732 | C | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3360C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346732 | |||||||
| chr6:55346828 | A | G | 2 | a0002c0002t0003g0091 a0002c0002t0003g0092 |
2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.317-3264A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346828 | |||||||
| chr6:55346831 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3261T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346831 | |||||||
| chr6:55346841 | C | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3251C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346841 | |||||||
| chr6:55346841 | C | CA | 6 | a0001c0005t0003g0228 a0001c0005t0003g0229 a0001c0005t0003g0230 others(3): Show |
7 | HG02896.hp1 HG02897.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.317-3251_317-3250i others(3): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346841 | |||||||
| chr6:55346842 | C | A | 46 | a0001c0001t0001g0041 a0001c0001t0001g0213 a0001c0001t0001g0214 others(43): Show |
49 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.317-3250C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346842 | |||||||
| chr6:55346842 | C | CA | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(144): Show |
175 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.317-3242dupA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55346842 | ||||||
| chr6:55346842 | C | CAA | 5 | a0001c0001t0004g0027 a0001c0001t0004g0274 a0001c0005t0003g0226 others(2): Show |
6 | HG01257.hp1 HG01258.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-3243_317-3242d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55346842 | ||||||
| chr6:55346842 | C | CCA | 118 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(115): Show |
136 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(133): Show |
intron_variant | MODIFIER | c.317-3250_317-3249i others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346842 | |||||||
| chr6:55346843 | A | C | 1 | a0004c0004t0002g0200 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.317-3249A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346843 | |||||||
| chr6:55346866 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-3226G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346866 | |||||||
| chr6:55346900 | C | T | 1 | a0001c0005t0003g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.317-3192C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346900 | |||||||
| chr6:55346970 | G | A | 21 | a0002c0002t0003g0024 a0002c0002t0003g0236 a0002c0002t0003g0254 others(18): Show |
23 | HG02040.hp2 HG02145.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.317-3122G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346970 | |||||||
| chr6:55346988 | C | T | 1 | a0001c0001t0006g0219 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.317-3104C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55346988 | |||||||
| chr6:55347014 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.317-3078T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347014 | |||||||
| chr6:55347097 | C | T | 9 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0004g0164 others(6): Show |
10 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.317-2995C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347097 | |||||||
| chr6:55347125 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-2967T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347125 | |||||||
| chr6:55347127 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-2965T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347127 | |||||||
| chr6:55347144 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-2948G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347144 | |||||||
| chr6:55347171 | C | T | 7 | a0002c0002t0003g0024 a0002c0002t0003g0254 a0002c0002t0003g0255 others(4): Show |
8 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.317-2921C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347171 | |||||||
| chr6:55347209 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-2883T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347209 | |||||||
| chr6:55347240 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-2852A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347240 | |||||||
| chr6:55347266 | G | A | 106 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(103): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.317-2826G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347266 | |||||||
| chr6:55347333 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-2759T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347333 | |||||||
| chr6:55347423 | G | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-2669G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347423 | |||||||
| chr6:55347464 | C | T | 1 | a0002c0002t0004g0112 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.317-2628C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347464 | |||||||
| chr6:55347490 | G | A | 5 | a0004c0004t0002g0035 a0004c0004t0002g0325 a0004c0004t0002g0326 others(2): Show |
6 | HG02451.hp1 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-2602G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347490 | |||||||
| chr6:55347515 | G | A | 1 | a0001c0001t0004g0280 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.317-2577G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347515 | |||||||
| chr6:55347516 | G | T | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.317-2576G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347516 | |||||||
| chr6:55347517 | G | A | 3 | a0001c0001t0004g0008 a0001c0001t0004g0028 a0001c0001t0004g0281 |
6 | NA18953.hp1 NA18966.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-2575G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347517 | |||||||
| chr6:55347522 | A | G | 1 | a0001c0001t0003g0314 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.317-2570A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347522 | |||||||
| chr6:55347860 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-2232C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347860 | |||||||
| chr6:55347991 | AG | A | 7 | a0002c0002t0003g0024 a0002c0002t0003g0254 a0002c0002t0003g0255 others(4): Show |
8 | HG02145.hp1 HG02257.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.317-2100delG | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55347991 | |||||||
| chr6:55348016 | T | C | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.317-2076T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348016 | |||||||
| chr6:55348035 | T | G | 106 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(103): Show |
125 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.317-2057T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348035 | |||||||
| chr6:55348039 | G | A | 1 | a0001c0001t0003g0322 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.317-2053G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348039 | |||||||
| chr6:55348108 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-1984C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348108 | |||||||
| chr6:55348186 | G | A | 259 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(256): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.317-1906G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348186 | |||||||
| chr6:55348237 | A | AGT | 74 | a0001c0001t0006g0329 a0001c0001t0011g0040 a0002c0002t0001g0104 others(71): Show |
79 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.317-1834_317-1833d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55348237 | ||||||
| chr6:55348237 | A | AGTGT | 67 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0002c0002t0001g0058 others(64): Show |
76 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(73): Show |
intron_variant | MODIFIER | c.317-1836_317-1833d others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55348237 | ||||||
| chr6:55348237 | A | AGTGTGT | 6 | a0002c0002t0003g0088 a0002c0002t0003g0089 a0002c0002t0003g0090 others(3): Show |
6 | HG00642.hp1 HG01074.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.317-1838_317-1833d others(8): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55348237 | ||||||
| chr6:55348237 | AGT | A | 104 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(101): Show |
123 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.317-1834_317-1833d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55348237 | ||||||
| chr6:55348259 | T | C | 1 | a0004c0004t0002g0282 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.317-1833T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348259 | |||||||
| chr6:55348461 | A | G | 5 | a0002c0002t0001g0087 a0002c0002t0003g0088 a0002c0002t0003g0089 others(2): Show |
5 | HG00642.hp1 HG01074.hp1 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-1631A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348461 | |||||||
| chr6:55348503 | A | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-1589A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348503 | |||||||
| chr6:55348504 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-1588G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348504 | |||||||
| chr6:55348547 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-1545T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348547 | |||||||
| chr6:55348595 | A | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-1497A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348595 | |||||||
| chr6:55348632 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-1460A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348632 | |||||||
| chr6:55348729 | A | G | 1 | a0001c0001t0004g0265 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.317-1363A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348729 | |||||||
| chr6:55348767 | G | T | 3 | a0002c0002t0003g0088 a0002c0002t0003g0089 a0002c0002t0003g0090 |
3 | HG00642.hp1 HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.317-1325G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348767 | |||||||
| chr6:55348784 | G | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-1308G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348784 | |||||||
| chr6:55348786 | A | T | 3 | a0002c0002t0003g0088 a0002c0002t0003g0089 a0002c0002t0003g0090 |
3 | HG00642.hp1 HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.317-1306A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348786 | |||||||
| chr6:55348832 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-1260T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348832 | |||||||
| chr6:55348860 | C | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-1232C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348860 | |||||||
| chr6:55348913 | G | C | 3 | a0003c0003t0002g0114 a0003c0003t0002g0119 a0003c0003t0002g0330 |
3 | HG00621.hp1 HG00673.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.317-1179G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348913 | |||||||
| chr6:55348914 | G | A | 1 | a0003c0003t0002g0119 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.317-1178G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348914 | |||||||
| chr6:55348933 | T | A | 3 | a0003c0003t0002g0103 a0003c0003t0002g0127 a0003c0003t0002g0141 |
3 | HG01256.hp2 HG02723.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.317-1159T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348933 | |||||||
| chr6:55348985 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-1107T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55348985 | |||||||
| chr6:55349060 | G | A | 11 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0004g0164 others(8): Show |
12 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.317-1032G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349060 | |||||||
| chr6:55349082 | A | C | 5 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0004c0004t0002g0023 others(2): Show |
6 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-1010A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349082 | |||||||
| chr6:55349177 | G | A | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.317-915G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349177 | |||||||
| chr6:55349321 | T | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-771T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349321 | |||||||
| chr6:55349374 | T | G | 2 | a0001c0001t0004g0260 a0001c0001t0004g0261 |
2 | NA18941.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.317-718T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349374 | |||||||
| chr6:55349443 | A | G | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.317-649A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349443 | |||||||
| chr6:55349536 | C | G | 2 | a0002c0002t0003g0139 a0002c0002t0003g0331 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.317-556C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349536 | |||||||
| chr6:55349613 | A | G | 1 | a0002c0002t0001g0086 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.317-479A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349613 | |||||||
| chr6:55349693 | A | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-399A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349693 | |||||||
| chr6:55349711 | G | A | 43 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0087 others(40): Show |
48 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.317-381G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349711 | |||||||
| chr6:55349728 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-364A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349728 | |||||||
| chr6:55349754 | A | C | 1 | a0001c0001t0001g0192 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.317-338A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349754 | |||||||
| chr6:55349757 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01106.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.317-335C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349757 | |||||||
| chr6:55349763 | G | GT | 19 | a0001c0001t0001g0097 a0001c0001t0001g0185 a0001c0001t0001g0186 others(16): Show |
19 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.317-313dupT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55349763 | ||||||
| chr6:55349763 | GT | G | 140 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(137): Show |
164 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.317-313delT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55349763 | ||||||
| chr6:55349789 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-303G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349789 | |||||||
| chr6:55349850 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-242A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349850 | |||||||
| chr6:55349879 | A | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-213A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349879 | |||||||
| chr6:55349895 | A | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.317-197A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | chr6 | 55349895 | |||||||
| chr6:55350010 | C | CA | 3 | a0001c0001t0001g0007 a0001c0001t0001g0270 a0001c0001t0001g0271 |
5 | HG00099.hp1 HG01070.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-81dupA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr6 | 55350010 | ||||||
| chr6:55350241 | C | G | 1 | a0001c0001t0004g0265 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.370+96C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350241 | |||||||
| chr6:55350269 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.370+124T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350269 | |||||||
| chr6:55350281 | G | A | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(313): Show |
365 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(362): Show |
intron_variant | MODIFIER | c.370+136G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350281 | |||||||
| chr6:55350357 | C | T | 136 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(133): Show |
159 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.370+212C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350357 | |||||||
| chr6:55350392 | A | C | 93 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(90): Show |
111 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.370+247A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350392 | |||||||
| chr6:55350461 | T | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(135): Show |
161 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.370+316T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350461 | |||||||
| chr6:55350560 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.370+415T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350560 | |||||||
| chr6:55350747 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.371-506C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350747 | |||||||
| chr6:55350762 | G | C | 20 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(17): Show |
21 | HG00099.hp2 HG01255.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.371-491G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350762 | |||||||
| chr6:55350815 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.371-438A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350815 | |||||||
| chr6:55350829 | A | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.371-424A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350829 | |||||||
| chr6:55350922 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.371-331C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350922 | |||||||
| chr6:55350954 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.371-299G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55350954 | |||||||
| chr6:55351015 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.371-238G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55351015 | |||||||
| chr6:55351070 | A | G | 93 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(90): Show |
111 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.371-183A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55351070 | |||||||
| chr6:55351088 | G | T | 1 | a0003c0003t0002g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.371-165G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55351088 | |||||||
| chr6:55351144 | T | C | 1 | a0001c0001t0003g0018 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.371-109T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55351144 | |||||||
| chr6:55351207 | G | A | 136 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(133): Show |
159 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.371-46G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 4/8 | chr6 | 55351207 | |||||||
| chr6:55351663 | A | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.701+80A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55351663 | |||||||
| chr6:55351853 | G | T | 10 | a0002c0002t0003g0120 a0002c0002t0003g0139 a0002c0002t0003g0331 others(7): Show |
10 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.701+270G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55351853 | |||||||
| chr6:55351880 | C | T | 1 | a0001c0001t0004g0273 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.701+297C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55351880 | |||||||
| chr6:55351889 | A | T | 14 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0004g0164 others(11): Show |
16 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.701+306A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55351889 | |||||||
| chr6:55351891 | A | G | 44 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0087 others(41): Show |
49 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.701+308A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55351891 | |||||||
| chr6:55351903 | A | AT | 39 | a0002c0002t0001g0058 a0002c0002t0001g0079 a0002c0002t0001g0087 others(36): Show |
43 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.701+330dupT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 55351903 | ||||||
| chr6:55351911 | T | G | 12 | a0001c0001t0003g0205 a0002c0002t0003g0120 a0002c0002t0003g0139 others(9): Show |
12 | HG01891.hp1 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.701+328T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55351911 | |||||||
| chr6:55351931 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.701+348G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55351931 | |||||||
| chr6:55351977 | C | T | 9 | a0001c0001t0003g0225 a0002c0002t0003g0024 a0002c0002t0003g0065 others(6): Show |
10 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.701+394C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55351977 | |||||||
| chr6:55352018 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.701+435G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352018 | |||||||
| chr6:55352080 | A | G | 1 | a0002c0002t0001g0151 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.701+497A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352080 | |||||||
| chr6:55352166 | C | A | 1 | a0003c0003t0002g0246 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.701+583C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352166 | |||||||
| chr6:55352314 | A | G | 3 | a0002c0002t0004g0154 a0002c0002t0004g0155 a0002c0002t0004g0156 |
3 | HG02486.hp2 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.701+731A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352314 | |||||||
| chr6:55352333 | G | A | 93 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(90): Show |
111 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.701+750G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352333 | |||||||
| chr6:55352378 | A | G | 1 | a0001c0001t0004g0164 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.701+795A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352378 | |||||||
| chr6:55352426 | G | A | 80 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(77): Show |
96 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.701+843G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352426 | |||||||
| chr6:55352441 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.701+858G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352441 | |||||||
| chr6:55352464 | G | T | 1 | a0003c0003t0002g0117 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.701+881G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352464 | |||||||
| chr6:55352528 | T | C | 1 | a0003c0003t0002g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.701+945T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352528 | |||||||
| chr6:55352616 | G | A | 2 | a0001c0001t0004g0283 a0001c0001t0004g0284 |
2 | NA19058.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.701+1033G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352616 | |||||||
| chr6:55352718 | A | G | 63 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(60): Show |
80 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.701+1135A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352718 | |||||||
| chr6:55352748 | A | G | 137 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(134): Show |
160 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.701+1165A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352748 | |||||||
| chr6:55352764 | T | C | 1 | a0003c0003t0002g0246 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.701+1181T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352764 | |||||||
| chr6:55352824 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.701+1241T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352824 | |||||||
| chr6:55352835 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.701+1252T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352835 | |||||||
| chr6:55352872 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.701+1289C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352872 | |||||||
| chr6:55352888 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.701+1305C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352888 | |||||||
| chr6:55352935 | A | T | 4 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0212 others(1): Show |
4 | HG02559.hp1 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+1352A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55352935 | |||||||
| chr6:55353011 | G | C | 1 | a0003c0003t0002g0128 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.701+1428G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353011 | |||||||
| chr6:55353015 | T | C | 138 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(135): Show |
161 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.701+1432T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353015 | |||||||
| chr6:55353072 | CAGTGAGG others(4): Show |
C | 1 | a0001c0001t0001g0310 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.701+1494_701+1504d others(13): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 55353072 | ||||||
| chr6:55353109 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.701+1526A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353109 | |||||||
| chr6:55353159 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.701+1576G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353159 | |||||||
| chr6:55353405 | C | G | 7 | a0001c0001t0004g0164 a0004c0004t0002g0035 a0004c0004t0002g0325 others(4): Show |
8 | HG02300.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.701+1822C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353405 | |||||||
| chr6:55353444 | A | T | 20 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(17): Show |
21 | HG00099.hp2 HG01255.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.701+1861A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353444 | |||||||
| chr6:55353455 | A | G | 1 | a0001c0001t0004g0184 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.701+1872A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353455 | |||||||
| chr6:55353473 | G | T | 92 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0036 others(89): Show |
110 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.701+1890G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353473 | |||||||
| chr6:55353529 | A | ATG | 7 | a0001c0001t0004g0164 a0004c0004t0002g0035 a0004c0004t0002g0325 others(4): Show |
8 | HG02300.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.701+1950_701+1951d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 55353529 | ||||||
| chr6:55353582 | T | G | 7 | a0001c0001t0004g0164 a0004c0004t0002g0035 a0004c0004t0002g0325 others(4): Show |
8 | HG02300.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.701+1999T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353582 | |||||||
| chr6:55353662 | A | G | 10 | a0002c0002t0003g0120 a0002c0002t0003g0139 a0002c0002t0003g0331 others(7): Show |
10 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.701+2079A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353662 | |||||||
| chr6:55353783 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.701+2200T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353783 | |||||||
| chr6:55353783 | T | C | 58 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0004g0164 others(55): Show |
65 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.701+2200T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353783 | |||||||
| chr6:55353784 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.701+2201T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353784 | |||||||
| chr6:55353876 | CACT | C | 9 | a0001c0005t0003g0226 a0001c0005t0003g0228 a0001c0005t0003g0229 others(6): Show |
10 | HG01884.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.701+2297_701+2299d others(5): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 55353876 | ||||||
| chr6:55353897 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.701+2314T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353897 | |||||||
| chr6:55353988 | G | A | 1 | a0004c0004t0002g0282 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.701+2405G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55353988 | |||||||
| chr6:55354003 | A | T | 1 | a0003c0003t0002g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.701+2420A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354003 | |||||||
| chr6:55354020 | A | G | 30 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(27): Show |
31 | HG00099.hp2 HG01255.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.701+2437A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354020 | |||||||
| chr6:55354043 | A | G | 6 | a0001c0001t0004g0164 a0004c0004t0002g0035 a0004c0004t0002g0325 others(3): Show |
7 | HG02451.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.701+2460A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354043 | |||||||
| chr6:55354146 | G | T | 1 | a0002c0002t0014g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.701+2563G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354146 | |||||||
| chr6:55354182 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(227): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.701+2599G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354182 | |||||||
| chr6:55354205 | G | A | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.701+2622G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354205 | |||||||
| chr6:55354233 | C | T | 1 | a0002c0002t0001g0149 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.701+2650C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354233 | |||||||
| chr6:55354259 | G | A | 9 | a0001c0001t0003g0225 a0002c0002t0003g0024 a0002c0002t0003g0065 others(6): Show |
10 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.701+2676G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354259 | |||||||
| chr6:55354353 | G | T | 2 | a0001c0001t0004g0026 a0001c0001t0004g0280 |
3 | HG02015.hp1 HG02074.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.701+2770G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354353 | |||||||
| chr6:55354368 | A | T | 8 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0004c0004t0002g0023 others(5): Show |
9 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.701+2785A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354368 | |||||||
| chr6:55354383 | A | C | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
31 | HG00099.hp2 HG01255.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.701+2800A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354383 | |||||||
| chr6:55354534 | A | C | 1 | a0002c0002t0004g0107 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.701+2951A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354534 | |||||||
| chr6:55354655 | T | A | 81 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(78): Show |
89 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.701+3072T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354655 | |||||||
| chr6:55354727 | G | A | 55 | a0001c0001t0001g0312 a0001c0001t0004g0311 a0002c0002t0001g0104 others(52): Show |
60 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.701+3144G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354727 | |||||||
| chr6:55354727 | G | C | 1 | a0001c0001t0004g0164 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.701+3144G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354727 | |||||||
| chr6:55354789 | C | G | 20 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(17): Show |
21 | HG00099.hp2 HG01255.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.701+3206C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354789 | |||||||
| chr6:55354929 | C | T | 1 | a0003c0003t0002g0330 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.701+3346C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55354929 | |||||||
| chr6:55355091 | A | C | 81 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(78): Show |
89 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.701+3508A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355091 | |||||||
| chr6:55355150 | T | G | 9 | a0001c0001t0003g0225 a0002c0002t0003g0024 a0002c0002t0003g0065 others(6): Show |
10 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.701+3567T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355150 | |||||||
| chr6:55355188 | A | G | 1 | a0001c0001t0004g0309 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.701+3605A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355188 | |||||||
| chr6:55355230 | T | G | 18 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(15): Show |
19 | HG00099.hp2 HG01255.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.701+3647T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355230 | |||||||
| chr6:55355286 | T | C | 1 | a0003c0003t0002g0256 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.702-3602T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355286 | |||||||
| chr6:55355296 | G | A | 80 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(77): Show |
88 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.702-3592G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355296 | |||||||
| chr6:55355318 | C | T | 8 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0004c0004t0002g0023 others(5): Show |
9 | HG01358.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.702-3570C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355318 | |||||||
| chr6:55355351 | A | T | 81 | a0001c0001t0001g0052 a0001c0001t0001g0213 a0001c0001t0001g0214 others(78): Show |
89 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.702-3537A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355351 | |||||||
| chr6:55355355 | T | TA | 7 | a0001c0001t0003g0018 a0001c0001t0003g0322 a0001c0001t0003g0323 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.702-3525dupA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 55355355 | ||||||
| chr6:55355383 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.702-3505A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355383 | |||||||
| chr6:55355396 | T | G | 7 | a0002c0002t0001g0146 a0002c0002t0001g0147 a0003c0003t0002g0004 others(4): Show |
10 | HG00544.hp2 HG00558.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.702-3492T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355396 | |||||||
| chr6:55355521 | A | G | 2 | a0004c0004t0002g0035 a0004c0004t0002g0328 |
3 | HG02895.hp1 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.702-3367A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355521 | |||||||
| chr6:55355527 | C | T | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
31 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.702-3361C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355527 | |||||||
| chr6:55355813 | AAGCTTTC | A | 6 | a0001c0001t0003g0322 a0001c0001t0003g0323 a0004c0004t0002g0321 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.702-3072_702-3066d others(9): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 55355813 | ||||||
| chr6:55355831 | C | T | 36 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(33): Show |
38 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.702-3057C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355831 | |||||||
| chr6:55355835 | T | C | 36 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(33): Show |
38 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.702-3053T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355835 | |||||||
| chr6:55355837 | A | G | 36 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(33): Show |
38 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.702-3051A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355837 | |||||||
| chr6:55355840 | T | C | 36 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(33): Show |
38 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.702-3048T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355840 | |||||||
| chr6:55355883 | C | G | 1 | a0001c0007t0004g0320 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.702-3005C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355883 | |||||||
| chr6:55355938 | C | T | 36 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(33): Show |
39 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.702-2950C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355938 | |||||||
| chr6:55355973 | A | G | 36 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(33): Show |
39 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.702-2915A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355973 | |||||||
| chr6:55355998 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.702-2890T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55355998 | |||||||
| chr6:55356025 | CTGAT | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(100): Show |
124 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.702-2857_702-2854d others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 55356025 | ||||||
| chr6:55356065 | G | C | 1 | a0001c0001t0006g0219 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.702-2823G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356065 | |||||||
| chr6:55356163 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(64): Show |
84 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.702-2725A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356163 | |||||||
| chr6:55356293 | T | A | 43 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(40): Show |
47 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.702-2595T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356293 | |||||||
| chr6:55356300 | T | G | 10 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0003c0003t0002g0056 others(7): Show |
11 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.702-2588T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356300 | |||||||
| chr6:55356415 | C | T | 332 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(329): Show |
383 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(380): Show |
intron_variant | MODIFIER | c.702-2473C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356415 | |||||||
| chr6:55356435 | G | A | 4 | a0004c0004t0002g0035 a0004c0004t0002g0325 a0004c0004t0002g0326 others(1): Show |
5 | HG02451.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.702-2453G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356435 | |||||||
| chr6:55356441 | T | C | 43 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(40): Show |
47 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.702-2447T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356441 | |||||||
| chr6:55356528 | C | T | 43 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(40): Show |
47 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.702-2360C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356528 | |||||||
| chr6:55356548 | T | G | 14 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0212 others(11): Show |
15 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.702-2340T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356548 | |||||||
| chr6:55356554 | A | G | 33 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0213 others(30): Show |
36 | HG00099.hp2 HG01074.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.702-2334A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356554 | |||||||
| chr6:55356586 | A | G | 52 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(49): Show |
56 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.702-2302A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356586 | |||||||
| chr6:55356597 | T | C | 43 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(40): Show |
47 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.702-2291T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356597 | |||||||
| chr6:55356643 | A | G | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.702-2245A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356643 | |||||||
| chr6:55356663 | G | T | 1 | a0002c0002t0014g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.702-2225G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356663 | |||||||
| chr6:55356776 | C | T | 43 | a0001c0001t0001g0167 a0001c0001t0001g0213 a0001c0001t0001g0214 others(40): Show |
47 | HG00099.hp2 HG00558.hp2 HG01074.hp2 others(44): Show |
intron_variant | MODIFIER | c.702-2112C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356776 | |||||||
| chr6:55356777 | G | A | 10 | a0001c0001t0003g0220 a0001c0001t0003g0322 a0001c0001t0003g0323 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.702-2111G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356777 | |||||||
| chr6:55356807 | A | G | 3 | a0001c0001t0003g0205 a0004c0004t0002g0206 a0005c0009t0002g0250 |
3 | HG02055.hp2 HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.702-2081A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356807 | |||||||
| chr6:55356931 | C | A | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.702-1957C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55356931 | |||||||
| chr6:55357074 | G | T | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.702-1814G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55357074 | |||||||
| chr6:55357330 | A | C | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.702-1558A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55357330 | |||||||
| chr6:55357421 | T | C | 1 | a0003c0003t0002g0237 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.702-1467T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55357421 | |||||||
| chr6:55357426 | A | ATC | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.702-1460_702-1459d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 55357426 | ||||||
| chr6:55357541 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.702-1347A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55357541 | |||||||
| chr6:55357586 | C | T | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.702-1302C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55357586 | |||||||
| chr6:55357600 | G | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.702-1288G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55357600 | |||||||
| chr6:55357713 | T | C | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.702-1175T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55357713 | |||||||
| chr6:55357749 | G | A | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.702-1139G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55357749 | |||||||
| chr6:55357835 | A | G | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.702-1053A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55357835 | |||||||
| chr6:55357870 | T | C | 2 | a0003c0003t0002g0022 a0003c0003t0002g0234 |
3 | HG02717.hp1 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.702-1018T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55357870 | |||||||
| chr6:55357898 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0192 others(78): Show |
97 | HG00323.hp1 HG00609.hp1 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.702-990A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55357898 | |||||||
| chr6:55358033 | C | T | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.702-855C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358033 | |||||||
| chr6:55358077 | G | T | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.702-811G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358077 | |||||||
| chr6:55358286 | A | C | 3 | a0002c0002t0004g0154 a0002c0002t0004g0155 a0002c0002t0004g0156 |
3 | HG02486.hp2 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.702-602A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358286 | |||||||
| chr6:55358321 | A | G | 1 | a0003c0003t0002g0242 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.702-567A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358321 | |||||||
| chr6:55358387 | T | C | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.702-501T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358387 | |||||||
| chr6:55358409 | A | G | 2 | a0003c0003t0002g0141 a0003c0003t0002g0233 |
2 | HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.702-479A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358409 | |||||||
| chr6:55358416 | A | C | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.702-472A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358416 | |||||||
| chr6:55358452 | G | A | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.702-436G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358452 | |||||||
| chr6:55358476 | A | C | 1 | a0002c0002t0010g0105 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.702-412A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358476 | |||||||
| chr6:55358480 | G | A | 58 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(55): Show |
65 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.702-408G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358480 | |||||||
| chr6:55358484 | A | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.702-404A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358484 | |||||||
| chr6:55358498 | C | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.702-390C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358498 | |||||||
| chr6:55358553 | G | A | 1 | a0004c0004t0002g0328 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.702-335G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358553 | |||||||
| chr6:55358573 | A | C | 1 | a0001c0001t0004g0305 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.702-315A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358573 | |||||||
| chr6:55358615 | A | G | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.702-273A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358615 | |||||||
| chr6:55358626 | A | G | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.702-262A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358626 | |||||||
| chr6:55358703 | T | G | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.702-185T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358703 | |||||||
| chr6:55358733 | A | G | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.702-155A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358733 | |||||||
| chr6:55358817 | G | A | 1 | a0004c0004t0005g0203 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.702-71G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 5/8 | chr6 | 55358817 | |||||||
| chr6:55359159 | T | C | 1 | a0004c0004t0002g0030 | 2 | NA18969.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.952+21T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359159 | |||||||
| chr6:55359164 | G | GTCTA | 93 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0192 others(90): Show |
112 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.952+45_952+48dupTA others(2): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55359164 | ||||||
| chr6:55359164 | G | GTCTATCT others(5): Show |
1 | a0003c0003t0002g0022 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.952+37_952+48dupTA others(10): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55359164 | ||||||
| chr6:55359164 | G | GTCTATCT others(9): Show |
23 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(20): Show |
24 | HG01074.hp2 HG01255.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.952+33_952+48dupTA others(14): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55359164 | ||||||
| chr6:55359164 | G | GTCTATCT others(13): Show |
6 | a0001c0001t0001g0213 a0003c0003t0002g0160 a0004c0004t0002g0035 others(3): Show |
7 | HG00099.hp2 HG02451.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.952+29_952+48dupTA others(18): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55359164 | ||||||
| chr6:55359164 | G | GTCTATCT others(17): Show |
10 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0003c0003t0002g0240 others(7): Show |
11 | HG01358.hp1 HG01891.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.952+48_952+49insTA others(22): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55359164 | ||||||
| chr6:55359177 | T | TCTAG | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+42_952+43insGC others(2): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55359177 | ||||||
| chr6:55359225 | A | G | 2 | a0001c0001t0004g0265 a0001c0001t0004g0266 |
2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.952+87A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359225 | |||||||
| chr6:55359287 | G | C | 3 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0004g0211 |
3 | HG02559.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.952+149G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359287 | |||||||
| chr6:55359309 | A | G | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.952+171A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359309 | |||||||
| chr6:55359337 | A | C | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.952+199A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359337 | |||||||
| chr6:55359363 | CTCTT | C | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.952+226_952+229del others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359363 | |||||||
| chr6:55359373 | T | A | 2 | a0003c0003t0002g0141 a0003c0003t0002g0233 |
2 | HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.952+235T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359373 | |||||||
| chr6:55359434 | T | G | 3 | a0001c0001t0003g0205 a0004c0004t0002g0206 a0005c0009t0002g0250 |
3 | HG02055.hp2 HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.952+296T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359434 | |||||||
| chr6:55359488 | C | A | 1 | a0001c0001t0004g0275 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.952+350C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359488 | |||||||
| chr6:55359562 | C | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+424C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359562 | |||||||
| chr6:55359609 | T | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+471T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359609 | |||||||
| chr6:55359619 | C | T | 1 | a0004c0004t0002g0222 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.952+481C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359619 | |||||||
| chr6:55359627 | G | C | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+489G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359627 | |||||||
| chr6:55359642 | G | A | 1 | a0003c0003t0002g0128 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.952+504G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359642 | |||||||
| chr6:55359748 | G | C | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+610G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55359748 | |||||||
| chr6:55360041 | G | A | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.952+903G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55360041 | |||||||
| chr6:55360141 | T | C | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+1003T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55360141 | |||||||
| chr6:55360212 | G | A | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+1074G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55360212 | |||||||
| chr6:55360260 | C | T | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.952+1122C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55360260 | |||||||
| chr6:55360395 | CATCTAT | C | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.952+1274_952+1279d others(8): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55360395 | ||||||
| chr6:55360500 | C | T | 2 | a0002c0002t0003g0082 a0002c0002t0003g0120 |
2 | HG01358.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.952+1362C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55360500 | |||||||
| chr6:55360508 | C | A | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.952+1370C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55360508 | |||||||
| chr6:55360554 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+1416A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55360554 | |||||||
| chr6:55360638 | A | G | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+1500A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55360638 | |||||||
| chr6:55360669 | A | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+1531A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55360669 | |||||||
| chr6:55360695 | T | G | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+1557T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55360695 | |||||||
| chr6:55360812 | A | T | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+1674A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55360812 | |||||||
| chr6:55361010 | A | G | 1 | a0001c0001t0004g0265 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.952+1872A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361010 | |||||||
| chr6:55361044 | A | T | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+1906A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361044 | |||||||
| chr6:55361080 | T | A | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.952+1942T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361080 | |||||||
| chr6:55361082 | G | C | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.952+1944G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361082 | |||||||
| chr6:55361101 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(248): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.952+1963G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361101 | |||||||
| chr6:55361215 | C | T | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+2077C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361215 | |||||||
| chr6:55361334 | G | A | 1 | a0003c0003t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.952+2196G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361334 | |||||||
| chr6:55361411 | C | T | 3 | a0001c0001t0003g0205 a0004c0004t0002g0206 a0005c0009t0002g0250 |
3 | HG02055.hp2 HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.952+2273C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361411 | |||||||
| chr6:55361472 | T | C | 10 | a0001c0001t0003g0220 a0001c0001t0003g0322 a0001c0001t0003g0323 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.952+2334T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361472 | |||||||
| chr6:55361522 | A | T | 59 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(56): Show |
66 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.952+2384A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361522 | |||||||
| chr6:55361569 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(76): Show |
94 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.952+2431C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361569 | |||||||
| chr6:55361591 | T | C | 4 | a0003c0003t0002g0123 a0003c0003t0002g0136 a0003c0003t0002g0142 others(1): Show |
4 | HG00639.hp1 HG02602.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.952+2453T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361591 | |||||||
| chr6:55361704 | G | A | 2 | a0003c0003t0002g0022 a0003c0003t0002g0234 |
3 | HG02717.hp1 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.952+2566G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361704 | |||||||
| chr6:55361760 | T | A | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+2622T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361760 | |||||||
| chr6:55361820 | C | T | 1 | a0002c0002t0003g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.952+2682C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361820 | |||||||
| chr6:55361833 | G | A | 64 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(61): Show |
73 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.952+2695G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361833 | |||||||
| chr6:55361938 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(76): Show |
94 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.952+2800C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55361938 | |||||||
| chr6:55362091 | A | G | 10 | a0001c0001t0003g0220 a0001c0001t0003g0322 a0001c0001t0003g0323 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.952+2953A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55362091 | |||||||
| chr6:55362244 | G | A | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.952+3106G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55362244 | |||||||
| chr6:55362274 | G | GA | 6 | a0001c0001t0001g0052 a0001c0001t0001g0189 a0002c0002t0003g0088 others(3): Show |
7 | HG02055.hp1 HG02602.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.952+3149dupA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55362274 | ||||||
| chr6:55362274 | GA | G | 43 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(40): Show |
47 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.952+3149delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55362274 | ||||||
| chr6:55362414 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(62): Show |
80 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.952+3276A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55362414 | |||||||
| chr6:55362515 | C | T | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+3377C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55362515 | |||||||
| chr6:55362533 | G | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+3395G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55362533 | |||||||
| chr6:55362606 | G | A | 1 | a0001c0001t0004g0264 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.952+3468G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55362606 | |||||||
| chr6:55362767 | T | C | 35 | a0001c0001t0003g0286 a0002c0002t0001g0058 a0002c0002t0001g0079 others(32): Show |
40 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.952+3629T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55362767 | |||||||
| chr6:55362795 | C | T | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+3657C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55362795 | |||||||
| chr6:55362846 | A | G | 3 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0004g0211 |
3 | HG02559.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.952+3708A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55362846 | |||||||
| chr6:55362885 | C | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(197): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.952+3747C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55362885 | |||||||
| chr6:55362999 | G | A | 3 | a0001c0001t0003g0205 a0004c0004t0002g0206 a0005c0009t0002g0250 |
3 | HG02055.hp2 HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.952+3861G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55362999 | |||||||
| chr6:55363055 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(76): Show |
94 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.952+3917G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363055 | |||||||
| chr6:55363132 | CA | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(237): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(271): Show |
intron_variant | MODIFIER | c.952+4004delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55363132 | ||||||
| chr6:55363180 | G | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+4042G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363180 | |||||||
| chr6:55363255 | G | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(197): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.952+4117G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363255 | |||||||
| chr6:55363302 | C | A | 1 | a0004c0004t0002g0197 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.952+4164C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363302 | |||||||
| chr6:55363364 | G | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(248): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.952+4226G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363364 | |||||||
| chr6:55363393 | T | C | 3 | a0003c0003t0002g0056 a0004c0004t0002g0023 a0004c0004t0002g0249 |
4 | HG01358.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.952+4255T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363393 | |||||||
| chr6:55363434 | C | CTT | 8 | a0001c0001t0003g0247 a0003c0003t0002g0141 a0003c0003t0002g0233 others(5): Show |
9 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.952+4309_952+4310d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55363434 | ||||||
| chr6:55363434 | CT | C | 38 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(35): Show |
43 | HG00099.hp2 HG00323.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.952+4310delT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55363434 | ||||||
| chr6:55363434 | CTT | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(191): Show |
223 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.952+4309_952+4310d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55363434 | ||||||
| chr6:55363570 | G | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(197): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.952+4432G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363570 | |||||||
| chr6:55363581 | TC | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(161): Show |
194 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.952+4449delC | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55363581 | ||||||
| chr6:55363587 | C | G | 36 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0043 others(33): Show |
37 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.952+4449C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363587 | |||||||
| chr6:55363588 | T | C | 37 | a0001c0001t0001g0015 a0001c0001t0001g0041 a0001c0001t0001g0043 others(34): Show |
38 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.952+4450T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363588 | |||||||
| chr6:55363588 | T | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(161): Show |
194 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.952+4450T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363588 | |||||||
| chr6:55363588 | TC | T | 8 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0003c0003t0002g0056 others(5): Show |
9 | HG01358.hp1 HG01891.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+4456delC | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55363588 | ||||||
| chr6:55363589 | C | T | 2 | a0003c0003t0002g0141 a0004c0004t0009g0251 |
2 | HG01256.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.952+4451C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363589 | |||||||
| chr6:55363602 | C | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(226): Show |
263 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.952+4464C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363602 | |||||||
| chr6:55363706 | C | T | 1 | a0003c0003t0002g0162 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.952+4568C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363706 | |||||||
| chr6:55363774 | T | C | 1 | a0001c0001t0004g0275 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.952+4636T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363774 | |||||||
| chr6:55363803 | C | T | 1 | a0003c0003t0002g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.952+4665C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363803 | |||||||
| chr6:55363817 | T | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(197): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.952+4679T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363817 | |||||||
| chr6:55363876 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+4738T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363876 | |||||||
| chr6:55363899 | C | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+4761C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363899 | |||||||
| chr6:55363900 | G | A | 3 | a0001c0001t0003g0205 a0004c0004t0002g0206 a0005c0009t0002g0250 |
3 | HG02055.hp2 HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.952+4762G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55363900 | |||||||
| chr6:55364008 | G | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+4870G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364008 | |||||||
| chr6:55364026 | A | G | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+4888A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364026 | |||||||
| chr6:55364044 | T | A | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+4906T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364044 | |||||||
| chr6:55364045 | G | A | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+4907G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364045 | |||||||
| chr6:55364094 | T | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+4956T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364094 | |||||||
| chr6:55364110 | C | A | 1 | a0003c0003t0002g0242 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.952+4972C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364110 | |||||||
| chr6:55364116 | A | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+4978A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364116 | |||||||
| chr6:55364117 | A | C | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+4979A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364117 | |||||||
| chr6:55364182 | C | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(197): Show |
231 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.952+5044C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364182 | |||||||
| chr6:55364228 | A | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+5090A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364228 | |||||||
| chr6:55364240 | T | A | 4 | a0002c0002t0003g0067 a0002c0002t0003g0075 a0002c0002t0003g0084 others(1): Show |
4 | NA18963.hp2 NA18966.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.952+5102T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364240 | |||||||
| chr6:55364265 | G | A | 1 | a0003c0003t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.952+5127G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364265 | |||||||
| chr6:55364309 | T | C | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+5171T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364309 | |||||||
| chr6:55364312 | T | G | 38 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(35): Show |
42 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.952+5174T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364312 | |||||||
| chr6:55364343 | T | G | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+5205T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364343 | |||||||
| chr6:55364348 | G | A | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+5210G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364348 | |||||||
| chr6:55364355 | T | G | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+5217T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364355 | |||||||
| chr6:55364362 | C | T | 1 | a0002c0002t0003g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.952+5224C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364362 | |||||||
| chr6:55364363 | G | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+5225G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364363 | |||||||
| chr6:55364380 | T | C | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+5242T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364380 | |||||||
| chr6:55364417 | T | G | 50 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(47): Show |
54 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.952+5279T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364417 | |||||||
| chr6:55364491 | C | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+5353C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364491 | |||||||
| chr6:55364549 | T | C | 3 | a0001c0001t0004g0283 a0001c0001t0004g0284 a0002c0002t0004g0085 |
3 | NA18960.hp2 NA19058.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.952+5411T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364549 | |||||||
| chr6:55364559 | T | G | 3 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0004g0211 |
3 | HG02559.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.952+5421T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364559 | |||||||
| chr6:55364578 | C | G | 1 | a0002c0002t0007g0064 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.952+5440C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364578 | |||||||
| chr6:55364626 | G | A | 3 | a0002c0002t0003g0088 a0002c0002t0003g0089 a0002c0002t0003g0090 |
3 | HG00642.hp1 HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.952+5488G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364626 | |||||||
| chr6:55364635 | T | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+5497T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364635 | |||||||
| chr6:55364653 | A | G | 2 | a0001c0001t0006g0329 a0001c0001t0011g0040 |
2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.952+5515A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364653 | |||||||
| chr6:55364754 | T | A | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+5616T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364754 | |||||||
| chr6:55364762 | G | T | 1 | a0004c0004t0002g0222 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.952+5624G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364762 | |||||||
| chr6:55364791 | G | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+5653G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364791 | |||||||
| chr6:55364800 | C | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+5662C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364800 | |||||||
| chr6:55364813 | C | G | 57 | a0001c0001t0003g0209 a0001c0001t0003g0225 a0001c0001t0003g0286 others(54): Show |
64 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.952+5675C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364813 | |||||||
| chr6:55364817 | T | C | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+5679T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364817 | |||||||
| chr6:55364888 | G | T | 1 | a0001c0001t0003g0223 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.952+5750G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364888 | |||||||
| chr6:55364935 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.952+5797T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364935 | |||||||
| chr6:55364938 | A | G | 1 | a0003c0003t0002g0241 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.952+5800A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364938 | |||||||
| chr6:55364946 | T | A | 3 | a0003c0003t0002g0114 a0003c0003t0002g0119 a0003c0003t0002g0330 |
3 | HG00621.hp1 HG00673.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.952+5808T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364946 | |||||||
| chr6:55364976 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(270): Show |
315 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(312): Show |
intron_variant | MODIFIER | c.952+5838A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55364976 | |||||||
| chr6:55365014 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0270 a0001c0001t0001g0271 |
5 | HG00099.hp1 HG01070.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.952+5876G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365014 | |||||||
| chr6:55365051 | T | C | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+5913T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365051 | |||||||
| chr6:55365062 | T | G | 1 | a0001c0001t0004g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.952+5924T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365062 | |||||||
| chr6:55365063 | A | T | 2 | a0003c0003t0002g0137 a0003c0003t0002g0138 |
2 | HG00741.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.952+5925A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365063 | |||||||
| chr6:55365064 | C | A | 1 | a0001c0001t0003g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.952+5926C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365064 | |||||||
| chr6:55365109 | T | A | 1 | a0001c0001t0001g0190 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.952+5971T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365109 | |||||||
| chr6:55365122 | T | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+5984T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365122 | |||||||
| chr6:55365198 | G | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+6060G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365198 | |||||||
| chr6:55365222 | T | A | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+6084T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365222 | |||||||
| chr6:55365235 | C | G | 2 | a0004c0004t0002g0034 a0004c0004t0002g0332 |
3 | NA18970.hp2 NA18989.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.952+6097C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365235 | |||||||
| chr6:55365351 | G | T | 22 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(19): Show |
23 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.952+6213G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365351 | |||||||
| chr6:55365352 | G | T | 22 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(19): Show |
23 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.952+6214G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365352 | |||||||
| chr6:55365353 | G | T | 1 | a0001c0001t0001g0176 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.952+6215G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365353 | |||||||
| chr6:55365376 | C | G | 57 | a0001c0001t0003g0209 a0001c0001t0003g0225 a0001c0001t0003g0286 others(54): Show |
64 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.952+6238C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365376 | |||||||
| chr6:55365377 | A | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+6239A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365377 | |||||||
| chr6:55365415 | A | T | 1 | a0002c0002t0003g0334 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.952+6277A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365415 | |||||||
| chr6:55365484 | G | A | 6 | a0001c0001t0003g0020 a0001c0001t0003g0223 a0001c0001t0006g0219 others(3): Show |
8 | HG00323.hp2 HG01069.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+6346G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365484 | |||||||
| chr6:55365500 | G | T | 2 | a0001c0005t0003g0229 a0001c0005t0003g0230 |
2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.952+6362G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365500 | |||||||
| chr6:55365592 | T | G | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.952+6454T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365592 | |||||||
| chr6:55365608 | T | C | 52 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(49): Show |
56 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.952+6470T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365608 | |||||||
| chr6:55365609 | G | A | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+6471G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365609 | |||||||
| chr6:55365651 | G | A | 2 | a0001c0005t0003g0226 a0004c0008t0002g0227 |
2 | HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.952+6513G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365651 | |||||||
| chr6:55365710 | G | C | 3 | a0002c0002t0001g0109 a0002c0002t0001g0122 a0002c0002t0004g0118 |
3 | HG01361.hp1 HG01361.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.952+6572G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365710 | |||||||
| chr6:55365711 | C | T | 3 | a0002c0002t0001g0109 a0002c0002t0001g0122 a0002c0002t0004g0118 |
3 | HG01361.hp1 HG01361.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.952+6573C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365711 | |||||||
| chr6:55365754 | G | T | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+6616G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365754 | |||||||
| chr6:55365773 | C | A | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+6635C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365773 | |||||||
| chr6:55365806 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+6668G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365806 | |||||||
| chr6:55365817 | G | T | 1 | a0001c0001t0003g0314 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.952+6679G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365817 | |||||||
| chr6:55365836 | T | G | 2 | a0003c0003t0002g0159 a0003c0003t0002g0161 |
2 | HG00642.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.952+6698T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365836 | |||||||
| chr6:55365858 | T | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(249): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.952+6720T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365858 | |||||||
| chr6:55365883 | A | G | 1 | a0001c0001t0004g0281 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.952+6745A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365883 | |||||||
| chr6:55365921 | C | A | 3 | a0001c0001t0003g0205 a0004c0004t0002g0206 a0005c0009t0002g0250 |
3 | HG02055.hp2 HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.952+6783C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365921 | |||||||
| chr6:55365935 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(249): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.952+6797T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365935 | |||||||
| chr6:55365938 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+6800A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365938 | |||||||
| chr6:55365968 | G | A | 4 | a0004c0004t0002g0035 a0004c0004t0002g0325 a0004c0004t0002g0326 others(1): Show |
5 | HG02451.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.952+6830G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55365968 | |||||||
| chr6:55366071 | T | G | 7 | a0002c0002t0010g0105 a0003c0003t0002g0130 a0003c0003t0002g0131 others(4): Show |
7 | HG00741.hp1 HG01169.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.952+6933T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366071 | |||||||
| chr6:55366082 | G | C | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+6944G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366082 | |||||||
| chr6:55366169 | G | T | 3 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0004g0211 |
3 | HG02559.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.952+7031G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366169 | |||||||
| chr6:55366184 | G | A | 6 | a0001c0001t0003g0020 a0001c0001t0003g0223 a0001c0001t0006g0219 others(3): Show |
8 | HG00323.hp2 HG01069.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+7046G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366184 | |||||||
| chr6:55366198 | T | A | 1 | a0001c0001t0004g0028 | 2 | NA18966.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.952+7060T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366198 | |||||||
| chr6:55366205 | T | C | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+7067T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366205 | |||||||
| chr6:55366254 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(249): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.952+7116A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366254 | |||||||
| chr6:55366264 | T | C | 3 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0004g0211 |
3 | HG02559.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.952+7126T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366264 | |||||||
| chr6:55366277 | G | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+7139G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366277 | |||||||
| chr6:55366291 | C | G | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.952+7153C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366291 | |||||||
| chr6:55366308 | G | A | 1 | a0004c0004t0002g0326 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.952+7170G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366308 | |||||||
| chr6:55366355 | T | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+7217T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366355 | |||||||
| chr6:55366446 | T | C | 12 | a0001c0001t0003g0210 a0001c0001t0003g0247 a0001c0001t0003g0248 others(9): Show |
13 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.952+7308T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366446 | |||||||
| chr6:55366468 | C | G | 10 | a0001c0001t0003g0220 a0001c0001t0003g0322 a0001c0001t0003g0323 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.952+7330C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366468 | |||||||
| chr6:55366478 | G | T | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+7340G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366478 | |||||||
| chr6:55366479 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+7341C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366479 | |||||||
| chr6:55366480 | T | C | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+7342T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366480 | |||||||
| chr6:55366503 | T | C | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+7365T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366503 | |||||||
| chr6:55366526 | C | T | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+7388C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366526 | |||||||
| chr6:55366534 | G | C | 2 | a0004c0004t0002g0023 a0004c0004t0002g0249 |
3 | HG01358.hp1 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.952+7396G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366534 | |||||||
| chr6:55366543 | T | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0192 others(78): Show |
97 | HG00323.hp1 HG00609.hp1 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.952+7405T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366543 | |||||||
| chr6:55366581 | C | G | 53 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(50): Show |
57 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(54): Show |
intron_variant | MODIFIER | c.952+7443C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366581 | |||||||
| chr6:55366615 | T | C | 42 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(39): Show |
46 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(43): Show |
intron_variant | MODIFIER | c.952+7477T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366615 | |||||||
| chr6:55366636 | TTG | T | 6 | a0001c0001t0003g0020 a0001c0001t0003g0223 a0001c0001t0006g0219 others(3): Show |
8 | HG00323.hp2 HG01069.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+7502_952+7503d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55366636 | ||||||
| chr6:55366646 | G | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(62): Show |
80 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.952+7508G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366646 | |||||||
| chr6:55366651 | G | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(248): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.952+7513G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366651 | |||||||
| chr6:55366690 | C | T | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+7552C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366690 | |||||||
| chr6:55366700 | C | G | 2 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
2 | NA18939.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.952+7562C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366700 | |||||||
| chr6:55366746 | T | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+7608T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366746 | |||||||
| chr6:55366796 | G | A | 2 | a0003c0003t0002g0256 a0004c0004t0002g0201 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.952+7658G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366796 | |||||||
| chr6:55366806 | T | C | 1 | a0001c0001t0008g0169 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.952+7668T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366806 | |||||||
| chr6:55366843 | A | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+7705A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366843 | |||||||
| chr6:55366848 | G | A | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+7710G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366848 | |||||||
| chr6:55366859 | A | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+7721A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366859 | |||||||
| chr6:55366867 | G | A | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+7729G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366867 | |||||||
| chr6:55366883 | G | A | 1 | a0001c0001t0004g0257 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.952+7745G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366883 | |||||||
| chr6:55366899 | G | GA | 30 | a0001c0001t0001g0177 a0001c0001t0001g0213 a0001c0001t0001g0214 others(27): Show |
33 | HG00099.hp2 HG01074.hp2 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.952+7768dupA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55366899 | ||||||
| chr6:55366910 | A | G | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.952+7772A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366910 | |||||||
| chr6:55366933 | G | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+7795G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366933 | |||||||
| chr6:55366958 | C | T | 14 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0004g0211 others(11): Show |
14 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+7820C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366958 | |||||||
| chr6:55366959 | G | A | 2 | a0001c0001t0003g0020 a0001c0001t0003g0223 |
3 | HG01069.hp1 HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.952+7821G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55366959 | |||||||
| chr6:55367013 | G | A | 1 | a0003c0003t0002g0252 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.952+7875G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367013 | |||||||
| chr6:55367113 | A | G | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.952+7975A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367113 | |||||||
| chr6:55367159 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(61): Show |
79 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.952+8021C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367159 | |||||||
| chr6:55367207 | C | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+8069C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367207 | |||||||
| chr6:55367288 | T | G | 50 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(47): Show |
54 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.952+8150T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367288 | |||||||
| chr6:55367299 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+8161T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367299 | |||||||
| chr6:55367354 | T | C | 1 | a0004c0004t0002g0030 | 2 | NA18969.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.952+8216T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367354 | |||||||
| chr6:55367364 | C | G | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+8226C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367364 | |||||||
| chr6:55367369 | C | T | 1 | a0001c0001t0001g0333 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.952+8231C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367369 | |||||||
| chr6:55367370 | G | A | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+8232G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367370 | |||||||
| chr6:55367375 | T | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+8237T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367375 | |||||||
| chr6:55367390 | G | T | 61 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(58): Show |
65 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(62): Show |
intron_variant | MODIFIER | c.952+8252G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367390 | |||||||
| chr6:55367455 | T | G | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.952+8317T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367455 | |||||||
| chr6:55367488 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(66): Show |
84 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.952+8350T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367488 | |||||||
| chr6:55367508 | C | T | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+8370C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367508 | |||||||
| chr6:55367537 | C | T | 8 | a0001c0001t0003g0020 a0001c0001t0003g0223 a0001c0001t0006g0219 others(5): Show |
11 | HG00323.hp2 HG01069.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.952+8399C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367537 | |||||||
| chr6:55367569 | G | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+8431G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367569 | |||||||
| chr6:55367580 | C | T | 9 | a0001c0005t0003g0226 a0001c0005t0003g0228 a0001c0005t0003g0229 others(6): Show |
10 | HG01884.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.952+8442C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367580 | |||||||
| chr6:55367610 | T | G | 3 | a0002c0002t0003g0011 a0002c0002t0003g0070 a0002c0002t0003g0071 |
4 | HG03239.hp1 HG03688.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.952+8472T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367610 | |||||||
| chr6:55367657 | C | A | 1 | a0002c0002t0010g0105 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.952+8519C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367657 | |||||||
| chr6:55367676 | T | G | 22 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(19): Show |
23 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.952+8538T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367676 | |||||||
| chr6:55367677 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0192 others(78): Show |
97 | HG00323.hp1 HG00609.hp1 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.952+8539A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367677 | |||||||
| chr6:55367688 | T | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+8550T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367688 | |||||||
| chr6:55367695 | T | G | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.952+8557T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367695 | |||||||
| chr6:55367757 | T | C | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+8619T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367757 | |||||||
| chr6:55367771 | C | T | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+8633C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367771 | |||||||
| chr6:55367818 | G | C | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+8680G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367818 | |||||||
| chr6:55367875 | T | C | 5 | a0001c0001t0003g0020 a0001c0001t0003g0223 a0004c0004t0002g0019 others(2): Show |
7 | HG00323.hp2 HG01069.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.952+8737T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367875 | |||||||
| chr6:55367974 | T | A | 5 | a0001c0001t0004g0027 a0001c0001t0004g0273 a0001c0001t0004g0274 others(2): Show |
6 | HG00323.hp1 HG00738.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.952+8836T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367974 | |||||||
| chr6:55367994 | C | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+8856C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55367994 | |||||||
| chr6:55368142 | T | C | 1 | a0001c0001t0004g0262 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.952+9004T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368142 | |||||||
| chr6:55368159 | C | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+9021C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368159 | |||||||
| chr6:55368199 | C | T | 6 | a0001c0001t0003g0020 a0001c0001t0003g0223 a0001c0001t0006g0219 others(3): Show |
8 | HG00323.hp2 HG01069.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+9061C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368199 | |||||||
| chr6:55368203 | C | T | 1 | a0003c0003t0002g0162 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.952+9065C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368203 | |||||||
| chr6:55368204 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+9066G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368204 | |||||||
| chr6:55368270 | C | G | 3 | a0004c0004t0005g0202 a0004c0004t0005g0203 a0004c0004t0005g0204 |
3 | HG02258.hp1 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.952+9132C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368270 | |||||||
| chr6:55368310 | T | A | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+9172T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368310 | |||||||
| chr6:55368347 | AT | A | 5 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0004g0211 others(2): Show |
5 | HG02559.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.952+9216delT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55368347 | ||||||
| chr6:55368375 | C | T | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+9237C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368375 | |||||||
| chr6:55368397 | G | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+9259G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368397 | |||||||
| chr6:55368430 | C | T | 1 | a0001c0001t0004g0304 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.952+9292C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368430 | |||||||
| chr6:55368474 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.952+9336G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368474 | |||||||
| chr6:55368515 | A | G | 22 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(19): Show |
23 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.952+9377A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368515 | |||||||
| chr6:55368594 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.952+9456T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368594 | |||||||
| chr6:55368606 | A | T | 1 | a0003c0003t0002g0119 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.952+9468A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368606 | |||||||
| chr6:55368701 | C | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+9563C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368701 | |||||||
| chr6:55368702 | T | A | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+9564T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368702 | |||||||
| chr6:55368734 | G | C | 1 | a0001c0001t0001g0259 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.952+9596G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368734 | |||||||
| chr6:55368863 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.952+9725T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368863 | |||||||
| chr6:55368865 | T | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+9727T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368865 | |||||||
| chr6:55368911 | A | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+9773A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368911 | |||||||
| chr6:55368913 | C | T | 9 | a0001c0005t0003g0226 a0001c0005t0003g0228 a0001c0005t0003g0229 others(6): Show |
10 | HG01884.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.952+9775C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368913 | |||||||
| chr6:55368915 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.952+9777C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368915 | |||||||
| chr6:55368973 | G | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+9835G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368973 | |||||||
| chr6:55368985 | C | A | 1 | a0002c0002t0003g0076 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.952+9847C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368985 | |||||||
| chr6:55368985 | C | T | 2 | a0001c0001t0004g0025 a0004c0004t0002g0285 |
3 | HG01074.hp2 NA18947.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.952+9847C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368985 | |||||||
| chr6:55368986 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.952+9848G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55368986 | |||||||
| chr6:55369023 | G | C | 1 | a0003c0003t0002g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.952+9885G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369023 | |||||||
| chr6:55369036 | C | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+9898C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369036 | |||||||
| chr6:55369043 | G | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+9905G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369043 | |||||||
| chr6:55369049 | T | C | 50 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(47): Show |
54 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.952+9911T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369049 | |||||||
| chr6:55369049 | T | G | 1 | a0003c0003t0002g0160 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.952+9911T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369049 | |||||||
| chr6:55369090 | C | T | 25 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(22): Show |
27 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.952+9952C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369090 | |||||||
| chr6:55369128 | T | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+9990T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369128 | |||||||
| chr6:55369141 | A | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+10003A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369141 | |||||||
| chr6:55369164 | G | A | 1 | a0001c0001t0008g0169 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.952+10026G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369164 | |||||||
| chr6:55369166 | C | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+10028C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369166 | |||||||
| chr6:55369170 | A | G | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+10032A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369170 | |||||||
| chr6:55369221 | A | G | 1 | a0003c0003t0002g0237 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.952+10083A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369221 | |||||||
| chr6:55369243 | G | T | 1 | a0001c0001t0004g0309 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.952+10105G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369243 | |||||||
| chr6:55369263 | C | T | 1 | a0003c0003t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.952+10125C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369263 | |||||||
| chr6:55369281 | A | G | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.952+10143A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369281 | |||||||
| chr6:55369304 | C | G | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.952+10166C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369304 | |||||||
| chr6:55369304 | C | T | 9 | a0001c0001t0003g0209 a0001c0001t0003g0225 a0002c0002t0003g0024 others(6): Show |
10 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.952+10166C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369304 | |||||||
| chr6:55369325 | G | C | 1 | a0002c0002t0003g0093 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.952+10187G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369325 | |||||||
| chr6:55369332 | G | A | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.952+10194G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369332 | |||||||
| chr6:55369354 | G | A | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+10216G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369354 | |||||||
| chr6:55369354 | G | T | 6 | a0001c0001t0003g0020 a0001c0001t0003g0223 a0001c0001t0006g0219 others(3): Show |
8 | HG00323.hp2 HG01069.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+10216G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369354 | |||||||
| chr6:55369374 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.952+10236C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369374 | |||||||
| chr6:55369375 | G | A | 170 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(167): Show |
190 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.952+10237G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369375 | |||||||
| chr6:55369406 | C | T | 1 | a0003c0003t0002g0119 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.952+10268C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369406 | |||||||
| chr6:55369409 | C | A | 1 | a0001c0001t0001g0213 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.952+10271C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369409 | |||||||
| chr6:55369419 | C | T | 10 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0003c0003t0002g0056 others(7): Show |
11 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.952+10281C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369419 | |||||||
| chr6:55369420 | G | A | 5 | a0002c0002t0004g0111 a0003c0003t0002g0013 a0003c0003t0002g0126 others(2): Show |
6 | HG01243.hp1 HG02132.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.952+10282G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369420 | |||||||
| chr6:55369429 | G | C | 2 | a0001c0001t0006g0329 a0001c0001t0011g0040 |
2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.952+10291G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369429 | |||||||
| chr6:55369524 | G | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(76): Show |
94 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.952+10386G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369524 | |||||||
| chr6:55369564 | GCAATTGT others(5): Show |
G | 4 | a0003c0003t0002g0110 a0003c0003t0002g0124 a0003c0003t0002g0133 others(1): Show |
4 | HG02080.hp2 NA19068.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.952+10429_952+1044 others(16): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55369564 | ||||||
| chr6:55369570 | G | A | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(326): Show |
380 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(377): Show |
intron_variant | MODIFIER | c.952+10432G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369570 | |||||||
| chr6:55369581 | CAT | C | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+10444_952+1044 others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369581 | |||||||
| chr6:55369597 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+10459G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369597 | |||||||
| chr6:55369603 | G | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+10465G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369603 | |||||||
| chr6:55369619 | A | T | 1 | a0003c0003t0002g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.952+10481A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369619 | |||||||
| chr6:55369626 | T | A | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+10488T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369626 | |||||||
| chr6:55369633 | A | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+10495A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369633 | |||||||
| chr6:55369656 | G | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+10518G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369656 | |||||||
| chr6:55369706 | A | C | 2 | a0003c0003t0002g0141 a0003c0003t0002g0233 |
2 | HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.952+10568A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369706 | |||||||
| chr6:55369709 | T | G | 2 | a0002c0002t0003g0091 a0002c0002t0003g0092 |
2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.952+10571T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369709 | |||||||
| chr6:55369714 | T | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+10576T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55369714 | |||||||
| chr6:55370125 | T | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+10987T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55370125 | |||||||
| chr6:55370125 | T | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0312 others(2): Show |
5 | HG01109.hp1 HG01192.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.952+10987T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55370125 | |||||||
| chr6:55370560 | T | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+11422T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55370560 | |||||||
| chr6:55370722 | A | G | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+11584A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55370722 | |||||||
| chr6:55370743 | A | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+11605A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55370743 | |||||||
| chr6:55370761 | T | C | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.952+11623T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55370761 | |||||||
| chr6:55370768 | A | C | 1 | a0001c0001t0004g0313 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.952+11630A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55370768 | |||||||
| chr6:55370812 | G | A | 1 | a0001c0001t0003g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.952+11674G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55370812 | |||||||
| chr6:55370855 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.952+11717A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55370855 | |||||||
| chr6:55370863 | A | G | 10 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0003c0003t0002g0056 others(7): Show |
11 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.952+11725A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55370863 | |||||||
| chr6:55370963 | C | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+11825C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55370963 | |||||||
| chr6:55371009 | G | A | 1 | a0003c0003t0002g0126 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.952+11871G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55371009 | |||||||
| chr6:55371069 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0099 others(3): Show |
7 | HG01175.hp1 HG01192.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.952+11931C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55371069 | |||||||
| chr6:55371117 | T | C | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+11979T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55371117 | |||||||
| chr6:55371147 | A | C | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.952+12009A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55371147 | |||||||
| chr6:55371195 | G | A | 3 | a0002c0002t0004g0154 a0002c0002t0004g0155 a0002c0002t0004g0156 |
3 | HG02486.hp2 HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.952+12057G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55371195 | |||||||
| chr6:55371475 | GA | G | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+12344delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55371475 | ||||||
| chr6:55371760 | G | C | 1 | a0002c0002t0003g0082 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.952+12622G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55371760 | |||||||
| chr6:55371781 | T | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+12643T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55371781 | |||||||
| chr6:55371807 | T | C | 2 | a0001c0001t0004g0260 a0001c0001t0004g0261 |
2 | NA18941.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.952+12669T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55371807 | |||||||
| chr6:55371857 | C | T | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+12719C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55371857 | |||||||
| chr6:55371870 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(82): Show |
102 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.952+12732C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55371870 | |||||||
| chr6:55372139 | C | T | 47 | a0001c0001t0003g0209 a0001c0001t0003g0225 a0001c0001t0003g0286 others(44): Show |
53 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.952+13001C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55372139 | |||||||
| chr6:55372365 | A | G | 10 | a0001c0001t0003g0220 a0001c0001t0003g0322 a0001c0001t0003g0323 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.952+13227A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55372365 | |||||||
| chr6:55372386 | C | T | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+13248C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55372386 | |||||||
| chr6:55372444 | A | G | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+13306A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55372444 | |||||||
| chr6:55372644 | C | T | 1 | a0002c0002t0014g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.952+13506C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55372644 | |||||||
| chr6:55372695 | C | A | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.952+13557C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55372695 | |||||||
| chr6:55372714 | T | C | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+13576T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55372714 | |||||||
| chr6:55372864 | C | T | 3 | a0001c0001t0003g0322 a0001c0001t0003g0323 a0004c0004t0002g0321 |
3 | HG02109.hp2 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.952+13726C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55372864 | |||||||
| chr6:55372879 | T | C | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+13741T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55372879 | |||||||
| chr6:55372925 | C | T | 10 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0003c0003t0002g0056 others(7): Show |
11 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.952+13787C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55372925 | |||||||
| chr6:55373030 | T | C | 1 | a0002c0002t0003g0082 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.952+13892T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373030 | |||||||
| chr6:55373044 | C | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(72): Show |
92 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.952+13906C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373044 | |||||||
| chr6:55373087 | C | CA | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(87): Show |
108 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.952+13964dupA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55373087 | ||||||
| chr6:55373087 | C | CAA | 12 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0218 others(9): Show |
12 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.952+13963_952+1396 others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55373087 | ||||||
| chr6:55373186 | A | G | 23 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(20): Show |
24 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.952+14048A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373186 | |||||||
| chr6:55373270 | T | C | 2 | a0003c0003t0002g0256 a0004c0004t0002g0201 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.952+14132T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373270 | |||||||
| chr6:55373279 | A | T | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.952+14141A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373279 | |||||||
| chr6:55373282 | G | A | 1 | a0003c0003t0002g0119 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.952+14144G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373282 | |||||||
| chr6:55373293 | C | T | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+14155C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373293 | |||||||
| chr6:55373318 | G | A | 1 | a0001c0001t0004g0275 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.952+14180G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373318 | |||||||
| chr6:55373481 | A | T | 10 | a0001c0001t0003g0220 a0001c0001t0003g0322 a0001c0001t0003g0323 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.952+14343A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373481 | |||||||
| chr6:55373535 | C | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(64): Show |
82 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.952+14397C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373535 | |||||||
| chr6:55373576 | C | G | 1 | a0001c0001t0001g0176 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.952+14438C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373576 | |||||||
| chr6:55373680 | A | G | 1 | a0003c0003t0002g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.952+14542A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373680 | |||||||
| chr6:55373708 | G | A | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.952+14570G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373708 | |||||||
| chr6:55373726 | T | G | 1 | a0001c0001t0001g0055 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.952+14588T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373726 | |||||||
| chr6:55373748 | C | CT | 85 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(82): Show |
95 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.952+14621dupT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55373748 | ||||||
| chr6:55373769 | G | A | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.952+14631G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373769 | |||||||
| chr6:55373788 | C | T | 22 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(19): Show |
23 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.952+14650C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373788 | |||||||
| chr6:55373789 | G | A | 1 | a0001c0001t0004g0274 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.952+14651G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373789 | |||||||
| chr6:55373796 | T | A | 1 | a0001c0001t0004g0283 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.952+14658T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373796 | |||||||
| chr6:55373899 | C | T | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+14761C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373899 | |||||||
| chr6:55373943 | T | C | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+14805T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373943 | |||||||
| chr6:55373998 | T | A | 1 | a0003c0003t0002g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.952+14860T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55373998 | |||||||
| chr6:55374049 | T | C | 1 | a0001c0001t0004g0283 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.952+14911T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374049 | |||||||
| chr6:55374051 | C | A | 1 | a0001c0001t0004g0283 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.952+14913C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374051 | |||||||
| chr6:55374071 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+14933A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374071 | |||||||
| chr6:55374098 | C | G | 1 | a0003c0003t0002g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.952+14960C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374098 | |||||||
| chr6:55374102 | G | C | 1 | a0003c0003t0002g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.952+14964G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374102 | |||||||
| chr6:55374106 | C | T | 1 | a0003c0003t0002g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.952+14968C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374106 | |||||||
| chr6:55374109 | A | AGCATATG others(22): Show |
1 | a0003c0003t0002g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.952+14971_952+1497 others(33): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374109 | |||||||
| chr6:55374184 | A | G | 116 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(113): Show |
130 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.952+15046A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374184 | |||||||
| chr6:55374214 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+15076A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374214 | |||||||
| chr6:55374253 | G | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+15115G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374253 | |||||||
| chr6:55374288 | T | A | 1 | a0001c0001t0001g0051 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.952+15150T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374288 | |||||||
| chr6:55374344 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(248): Show |
286 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(283): Show |
intron_variant | MODIFIER | c.952+15206C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374344 | |||||||
| chr6:55374610 | C | T | 3 | a0001c0001t0004g0302 a0001c0001t0004g0303 a0001c0001t0004g0318 |
3 | HG00609.hp1 NA19012.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.952+15472C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374610 | |||||||
| chr6:55374731 | T | C | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+15593T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374731 | |||||||
| chr6:55374738 | C | T | 1 | a0002c0002t0003g0082 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.952+15600C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374738 | |||||||
| chr6:55374739 | T | C | 1 | a0001c0001t0004g0275 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.952+15601T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374739 | |||||||
| chr6:55374743 | A | G | 1 | a0002c0002t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.952+15605A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374743 | |||||||
| chr6:55374817 | G | A | 2 | a0002c0002t0006g0125 a0003c0003t0002g0143 |
2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.952+15679G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374817 | |||||||
| chr6:55374836 | G | T | 2 | a0004c0004t0002g0197 a0004c0004t0002g0198 |
2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.952+15698G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374836 | |||||||
| chr6:55374840 | A | G | 3 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0004g0211 |
3 | HG02559.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.952+15702A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374840 | |||||||
| chr6:55374862 | T | A | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+15724T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374862 | |||||||
| chr6:55374881 | TC | T | 2 | a0001c0001t0004g0033 a0002c0002t0004g0112 |
3 | HG01069.hp2 HG01928.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.952+15745delC | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55374881 | ||||||
| chr6:55374894 | G | A | 2 | a0003c0003t0002g0141 a0003c0003t0002g0233 |
2 | HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.952+15756G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374894 | |||||||
| chr6:55374938 | C | T | 7 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0003c0003t0002g0056 others(4): Show |
8 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+15800C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55374938 | |||||||
| chr6:55375140 | T | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+16002T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55375140 | |||||||
| chr6:55375302 | G | A | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.952+16164G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55375302 | |||||||
| chr6:55375349 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.952+16211A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55375349 | |||||||
| chr6:55375709 | C | T | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+16571C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55375709 | |||||||
| chr6:55375716 | C | A | 2 | a0001c0005t0003g0229 a0001c0005t0003g0230 |
2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.952+16578C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55375716 | |||||||
| chr6:55375747 | T | A | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.952+16609T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55375747 | |||||||
| chr6:55375748 | A | T | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.952+16610A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55375748 | |||||||
| chr6:55375851 | C | T | 57 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(54): Show |
64 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.952+16713C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55375851 | |||||||
| chr6:55375875 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(84): Show |
104 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.952+16737C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55375875 | |||||||
| chr6:55375930 | T | G | 2 | a0001c0001t0001g0178 a0002c0002t0001g0086 |
2 | HG02015.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.952+16792T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55375930 | |||||||
| chr6:55375978 | A | G | 22 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(19): Show |
23 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.952+16840A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55375978 | |||||||
| chr6:55376037 | T | C | 58 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(55): Show |
65 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.952+16899T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55376037 | |||||||
| chr6:55376053 | A | G | 7 | a0004c0004t0002g0031 a0004c0004t0002g0279 a0004c0004t0002g0298 others(4): Show |
8 | HG01934.hp1 HG01978.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.952+16915A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55376053 | |||||||
| chr6:55376123 | T | A | 1 | a0004c0004t0002g0298 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.952+16985T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55376123 | |||||||
| chr6:55376268 | A | G | 2 | a0003c0003t0002g0141 a0003c0003t0002g0233 |
2 | HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.952+17130A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55376268 | |||||||
| chr6:55376320 | T | C | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+17182T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55376320 | |||||||
| chr6:55376369 | C | T | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+17231C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55376369 | |||||||
| chr6:55376405 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(84): Show |
104 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.952+17267A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55376405 | |||||||
| chr6:55376413 | G | A | 2 | a0003c0003t0002g0141 a0003c0003t0002g0233 |
2 | HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.952+17275G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55376413 | |||||||
| chr6:55376575 | G | A | 2 | a0001c0001t0003g0020 a0001c0001t0003g0223 |
3 | HG01069.hp1 HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.952+17437G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55376575 | |||||||
| chr6:55376754 | A | G | 2 | a0001c0001t0006g0329 a0001c0001t0011g0040 |
2 | HG02451.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.952+17616A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55376754 | |||||||
| chr6:55376773 | C | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(216): Show |
256 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.952+17635C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55376773 | |||||||
| chr6:55376845 | G | A | 1 | a0002c0002t0006g0125 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.952+17707G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55376845 | |||||||
| chr6:55377006 | T | A | 57 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(54): Show |
64 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.952+17868T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377006 | |||||||
| chr6:55377025 | C | G | 56 | a0001c0001t0003g0209 a0001c0001t0003g0225 a0001c0001t0003g0286 others(53): Show |
63 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.952+17887C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377025 | |||||||
| chr6:55377041 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.952+17903C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377041 | |||||||
| chr6:55377103 | A | G | 7 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0003c0003t0002g0056 others(4): Show |
8 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.952+17965A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377103 | |||||||
| chr6:55377134 | C | T | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+17996C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377134 | |||||||
| chr6:55377175 | A | G | 1 | a0002c0002t0003g0074 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.952+18037A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377175 | |||||||
| chr6:55377179 | C | G | 51 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(48): Show |
55 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.952+18041C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377179 | |||||||
| chr6:55377204 | T | C | 1 | a0002c0002t0001g0058 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.952+18066T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377204 | |||||||
| chr6:55377497 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.952+18359C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377497 | |||||||
| chr6:55377551 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0192 |
6 | NA18948.hp1 NA18952.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.952+18413T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377551 | |||||||
| chr6:55377672 | C | T | 1 | a0001c0001t0004g0027 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.952+18534C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377672 | |||||||
| chr6:55377780 | A | C | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+18642A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377780 | |||||||
| chr6:55377782 | A | G | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+18644A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377782 | |||||||
| chr6:55377782 | A | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0192 others(78): Show |
97 | HG00323.hp1 HG00609.hp1 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.952+18644A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377782 | |||||||
| chr6:55377806 | C | T | 1 | a0003c0003t0002g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.952+18668C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377806 | |||||||
| chr6:55377890 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.952+18752T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55377890 | |||||||
| chr6:55378062 | G | C | 3 | a0001c0001t0003g0322 a0001c0001t0003g0323 a0004c0004t0002g0321 |
3 | HG02109.hp2 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.952+18924G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378062 | |||||||
| chr6:55378068 | A | G | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.952+18930A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378068 | |||||||
| chr6:55378081 | T | C | 2 | a0004c0004t0002g0325 a0004c0004t0002g0326 |
2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.952+18943T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378081 | |||||||
| chr6:55378140 | G | A | 1 | a0001c0005t0003g0226 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.952+19002G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378140 | |||||||
| chr6:55378148 | G | T | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.952+19010G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378148 | |||||||
| chr6:55378159 | G | A | 4 | a0001c0001t0003g0209 a0002c0002t0003g0065 a0002c0002t0003g0254 others(1): Show |
4 | HG02280.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.952+19021G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378159 | |||||||
| chr6:55378191 | C | T | 4 | a0004c0004t0002g0035 a0004c0004t0002g0325 a0004c0004t0002g0326 others(1): Show |
5 | HG02451.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.952+19053C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378191 | |||||||
| chr6:55378220 | G | A | 1 | a0001c0001t0011g0040 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.952+19082G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378220 | |||||||
| chr6:55378351 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(206): Show |
240 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.952+19213C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378351 | |||||||
| chr6:55378548 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.952+19410A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378548 | |||||||
| chr6:55378620 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0187 |
2 | NA18961.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.952+19482C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378620 | |||||||
| chr6:55378695 | G | GT | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(64): Show |
82 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.952+19565dupT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55378695 | ||||||
| chr6:55378739 | A | C | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.952+19601A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378739 | |||||||
| chr6:55378937 | C | T | 3 | a0001c0001t0003g0314 a0001c0001t0004g0288 a0001c0001t0012g0297 |
3 | HG01169.hp2 HG01433.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.952+19799C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55378937 | |||||||
| chr6:55379036 | C | A | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.952+19898C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379036 | |||||||
| chr6:55379080 | G | A | 57 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(54): Show |
64 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.952+19942G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379080 | |||||||
| chr6:55379084 | G | C | 126 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(123): Show |
141 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.952+19946G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379084 | |||||||
| chr6:55379135 | T | A | 57 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(54): Show |
64 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.952+19997T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379135 | |||||||
| chr6:55379139 | A | G | 9 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(6): Show |
9 | HG01891.hp1 HG02280.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.952+20001A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379139 | |||||||
| chr6:55379250 | A | G | 1 | a0004c0004t0002g0197 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.953-19930A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379250 | |||||||
| chr6:55379389 | G | C | 30 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(27): Show |
33 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.953-19791G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379389 | |||||||
| chr6:55379427 | T | C | 4 | a0001c0001t0003g0205 a0003c0003t0002g0057 a0004c0004t0002g0206 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.953-19753T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379427 | |||||||
| chr6:55379510 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.953-19670A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379510 | |||||||
| chr6:55379515 | T | TA | 113 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(110): Show |
127 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.953-19665_953-1966 others(5): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379515 | |||||||
| chr6:55379534 | A | C | 1 | a0002c0002t0004g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.953-19646A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379534 | |||||||
| chr6:55379574 | TAC | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(185): Show |
221 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.953-19584_953-1958 others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55379574 | ||||||
| chr6:55379592 | CACACAA | C | 9 | a0001c0005t0003g0226 a0001c0005t0003g0228 a0001c0005t0003g0229 others(6): Show |
10 | HG01884.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.953-19585_953-1958 others(10): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55379592 | ||||||
| chr6:55379596 | CAA | C | 121 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(118): Show |
136 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.953-19582_953-1958 others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55379596 | ||||||
| chr6:55379598 | A | C | 12 | a0001c0001t0003g0209 a0001c0001t0003g0225 a0001c0001t0006g0329 others(9): Show |
13 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.953-19582A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379598 | |||||||
| chr6:55379837 | C | T | 8 | a0003c0003t0002g0066 a0003c0003t0002g0130 a0003c0003t0002g0131 others(5): Show |
8 | HG00741.hp1 HG01169.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-19343C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379837 | |||||||
| chr6:55379850 | G | A | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.953-19330G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379850 | |||||||
| chr6:55379880 | G | A | 2 | a0003c0003t0002g0141 a0003c0003t0002g0233 |
2 | HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.953-19300G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379880 | |||||||
| chr6:55379898 | G | A | 1 | a0002c0002t0003g0091 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.953-19282G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379898 | |||||||
| chr6:55379931 | G | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.953-19249G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55379931 | |||||||
| chr6:55380059 | T | G | 55 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(52): Show |
62 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.953-19121T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55380059 | |||||||
| chr6:55380083 | C | A | 56 | a0001c0001t0003g0209 a0001c0001t0003g0225 a0001c0001t0003g0286 others(53): Show |
63 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.953-19097C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55380083 | |||||||
| chr6:55380233 | C | A | 1 | a0003c0003t0002g0246 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.953-18947C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55380233 | |||||||
| chr6:55380318 | C | T | 2 | a0002c0002t0003g0073 a0002c0002t0003g0081 |
2 | NA18962.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.953-18862C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55380318 | |||||||
| chr6:55380510 | T | C | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-18670T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55380510 | |||||||
| chr6:55380595 | A | G | 1 | a0004c0004t0002g0221 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.953-18585A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55380595 | |||||||
| chr6:55380612 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-18568C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55380612 | |||||||
| chr6:55380729 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.953-18451C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55380729 | |||||||
| chr6:55380748 | G | C | 1 | a0002c0002t0003g0038 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.953-18432G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55380748 | |||||||
| chr6:55380785 | G | T | 1 | a0001c0001t0004g0028 | 2 | NA18966.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.953-18395G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55380785 | |||||||
| chr6:55380919 | C | T | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-18261C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55380919 | |||||||
| chr6:55381090 | C | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(238): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(273): Show |
intron_variant | MODIFIER | c.953-18090C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55381090 | |||||||
| chr6:55381310 | C | T | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-17870C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55381310 | |||||||
| chr6:55381355 | C | T | 1 | a0003c0003t0002g0110 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.953-17825C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55381355 | |||||||
| chr6:55381421 | T | A | 9 | a0001c0005t0003g0226 a0001c0005t0003g0228 a0001c0005t0003g0229 others(6): Show |
10 | HG01884.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.953-17759T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55381421 | |||||||
| chr6:55381452 | A | G | 1 | a0004c0004t0002g0317 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.953-17728A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55381452 | |||||||
| chr6:55381474 | C | T | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-17706C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55381474 | |||||||
| chr6:55381491 | G | A | 1 | a0004c0004t0002g0285 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.953-17689G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55381491 | |||||||
| chr6:55381522 | A | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-17658A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55381522 | |||||||
| chr6:55381679 | T | A | 3 | a0001c0001t0003g0205 a0004c0004t0002g0206 a0005c0009t0002g0250 |
3 | HG02055.hp2 HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.953-17501T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55381679 | |||||||
| chr6:55381827 | C | T | 2 | a0004c0004t0002g0023 a0004c0004t0002g0249 |
3 | HG01358.hp1 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.953-17353C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55381827 | |||||||
| chr6:55381876 | G | A | 2 | a0002c0002t0007g0061 a0002c0002t0007g0064 |
2 | HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.953-17304G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55381876 | |||||||
| chr6:55382307 | G | T | 1 | a0003c0003t0002g0130 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.953-16873G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55382307 | |||||||
| chr6:55382349 | A | G | 3 | a0001c0001t0003g0205 a0004c0004t0002g0206 a0005c0009t0002g0250 |
3 | HG02055.hp2 HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.953-16831A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55382349 | |||||||
| chr6:55382366 | G | A | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.953-16814G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55382366 | |||||||
| chr6:55382396 | A | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-16784A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55382396 | |||||||
| chr6:55382491 | G | T | 3 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0004g0211 |
3 | HG02559.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.953-16689G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55382491 | |||||||
| chr6:55382598 | T | G | 1 | a0001c0001t0001g0192 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.953-16582T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55382598 | |||||||
| chr6:55382611 | A | G | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-16569A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55382611 | |||||||
| chr6:55382711 | G | A | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-16469G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55382711 | |||||||
| chr6:55382869 | T | C | 1 | a0003c0003t0002g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.953-16311T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55382869 | |||||||
| chr6:55382902 | C | G | 1 | a0001c0001t0001g0195 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.953-16278C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55382902 | |||||||
| chr6:55383013 | C | T | 1 | a0002c0002t0003g0254 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.953-16167C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55383013 | |||||||
| chr6:55383211 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.953-15969G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55383211 | |||||||
| chr6:55383258 | TAAGGATC others(24): Show |
T | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-15920_953-1589 others(35): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55383258 | ||||||
| chr6:55383297 | C | T | 1 | a0002c0002t0003g0090 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.953-15883C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55383297 | |||||||
| chr6:55383332 | C | A | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-15848C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55383332 | |||||||
| chr6:55383360 | T | A | 1 | a0002c0002t0004g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.953-15820T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55383360 | |||||||
| chr6:55383485 | A | T | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-15695A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55383485 | |||||||
| chr6:55383604 | C | G | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-15576C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55383604 | |||||||
| chr6:55383780 | G | A | 1 | a0001c0001t0003g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.953-15400G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55383780 | |||||||
| chr6:55383890 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-15290G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55383890 | |||||||
| chr6:55383943 | A | T | 2 | a0001c0001t0004g0295 a0001c0001t0004g0296 |
2 | NA18612.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.953-15237A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55383943 | |||||||
| chr6:55383984 | T | C | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-15196T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55383984 | |||||||
| chr6:55384054 | T | A | 1 | a0001c0001t0004g0289 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.953-15126T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384054 | |||||||
| chr6:55384103 | C | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-15077C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384103 | |||||||
| chr6:55384131 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-15049G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384131 | |||||||
| chr6:55384270 | TA | T | 10 | a0001c0001t0003g0220 a0001c0001t0003g0322 a0001c0001t0003g0323 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.953-14902delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55384270 | ||||||
| chr6:55384303 | C | T | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-14877C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384303 | |||||||
| chr6:55384304 | AC | A | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-14875delC | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384304 | |||||||
| chr6:55384470 | C | T | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-14710C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384470 | |||||||
| chr6:55384481 | AT | A | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-14696delT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55384481 | ||||||
| chr6:55384559 | C | T | 1 | a0002c0002t0003g0071 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.953-14621C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384559 | |||||||
| chr6:55384661 | G | T | 1 | a0001c0001t0004g0164 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.953-14519G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384661 | |||||||
| chr6:55384852 | C | T | 4 | a0001c0001t0001g0294 a0001c0001t0004g0042 a0001c0001t0004g0295 others(1): Show |
4 | NA18612.hp1 NA18980.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-14328C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384852 | |||||||
| chr6:55384859 | G | A | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.953-14321G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384859 | |||||||
| chr6:55384863 | C | CA | 223 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0029 others(220): Show |
252 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.953-14301dupA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55384863 | ||||||
| chr6:55384863 | C | CAA | 13 | a0001c0001t0003g0209 a0001c0001t0003g0225 a0001c0001t0004g0028 others(10): Show |
15 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.953-14302_953-1430 others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55384863 | ||||||
| chr6:55384863 | CA | C | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-14301delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55384863 | ||||||
| chr6:55384863 | CAA | C | 13 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(10): Show |
14 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.953-14302_953-1430 others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55384863 | ||||||
| chr6:55384890 | G | C | 1 | a0002c0002t0003g0074 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.953-14290G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384890 | |||||||
| chr6:55384894 | C | T | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-14286C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384894 | |||||||
| chr6:55384935 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-14245A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55384935 | |||||||
| chr6:55385070 | T | C | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-14110T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385070 | |||||||
| chr6:55385391 | G | A | 2 | a0002c0002t0001g0108 a0002c0002t0001g0113 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.953-13789G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385391 | |||||||
| chr6:55385399 | G | A | 25 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(22): Show |
27 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(24): Show |
intron_variant | MODIFIER | c.953-13781G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385399 | |||||||
| chr6:55385438 | T | G | 21 | a0001c0001t0003g0314 a0001c0001t0004g0027 a0001c0001t0004g0033 others(18): Show |
23 | HG00323.hp1 HG00735.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.953-13742T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385438 | |||||||
| chr6:55385464 | C | T | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-13716C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385464 | |||||||
| chr6:55385532 | G | A | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.953-13648G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385532 | |||||||
| chr6:55385539 | A | G | 1 | a0003c0003t0002g0241 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.953-13641A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385539 | |||||||
| chr6:55385549 | T | A | 1 | a0001c0001t0001g0195 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.953-13631T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385549 | |||||||
| chr6:55385647 | C | T | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.953-13533C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385647 | |||||||
| chr6:55385648 | G | A | 9 | a0001c0001t0003g0209 a0001c0001t0003g0225 a0002c0002t0003g0024 others(6): Show |
10 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.953-13532G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385648 | |||||||
| chr6:55385663 | T | G | 1 | a0003c0003t0002g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.953-13517T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385663 | |||||||
| chr6:55385822 | A | G | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-13358A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385822 | |||||||
| chr6:55385866 | T | C | 1 | a0001c0001t0004g0289 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.953-13314T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385866 | |||||||
| chr6:55385914 | A | G | 2 | a0003c0003t0002g0137 a0003c0003t0002g0138 |
2 | HG00741.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.953-13266A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55385914 | |||||||
| chr6:55386012 | A | G | 2 | a0004c0004t0002g0023 a0004c0004t0002g0249 |
3 | HG01358.hp1 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.953-13168A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55386012 | |||||||
| chr6:55386041 | C | T | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-13139C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55386041 | |||||||
| chr6:55386238 | A | G | 2 | a0004c0004t0002g0023 a0004c0004t0002g0249 |
3 | HG01358.hp1 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.953-12942A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55386238 | |||||||
| chr6:55386265 | G | A | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-12915G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55386265 | |||||||
| chr6:55386272 | T | A | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-12908T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55386272 | |||||||
| chr6:55386440 | A | T | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-12740A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55386440 | |||||||
| chr6:55386527 | G | A | 7 | a0001c0001t0002g0224 a0001c0001t0003g0020 a0001c0001t0003g0223 others(4): Show |
9 | HG00323.hp2 HG01069.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-12653G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55386527 | |||||||
| chr6:55386598 | C | T | 1 | a0002c0002t0003g0080 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.953-12582C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55386598 | |||||||
| chr6:55386643 | A | G | 5 | a0001c0001t0003g0205 a0003c0003t0002g0141 a0003c0003t0002g0233 others(2): Show |
5 | HG01256.hp2 HG02055.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.953-12537A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55386643 | |||||||
| chr6:55386917 | C | G | 22 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(19): Show |
23 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.953-12263C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55386917 | |||||||
| chr6:55387101 | CA | C | 10 | a0001c0001t0003g0220 a0001c0001t0003g0322 a0001c0001t0003g0323 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.953-12075delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55387101 | ||||||
| chr6:55387452 | G | A | 1 | a0001c0001t0003g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.953-11728G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55387452 | |||||||
| chr6:55387499 | T | C | 10 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0003c0003t0002g0056 others(7): Show |
11 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.953-11681T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55387499 | |||||||
| chr6:55387540 | C | A | 1 | a0003c0003t0002g0238 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.953-11640C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55387540 | |||||||
| chr6:55387580 | G | T | 9 | a0001c0005t0003g0226 a0001c0005t0003g0228 a0001c0005t0003g0229 others(6): Show |
10 | HG01884.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.953-11600G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55387580 | |||||||
| chr6:55387689 | G | A | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-11491G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55387689 | |||||||
| chr6:55387798 | G | T | 1 | a0001c0001t0004g0164 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.953-11382G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55387798 | |||||||
| chr6:55387799 | C | T | 1 | a0001c0001t0004g0164 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.953-11381C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55387799 | |||||||
| chr6:55388020 | C | T | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-11160C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388020 | |||||||
| chr6:55388041 | G | C | 1 | a0002c0002t0004g0094 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.953-11139G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388041 | |||||||
| chr6:55388053 | C | G | 1 | a0003c0003t0002g0162 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.953-11127C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388053 | |||||||
| chr6:55388073 | A | G | 2 | a0003c0003t0002g0160 a0003c0003t0002g0240 |
2 | HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.953-11107A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388073 | |||||||
| chr6:55388126 | A | G | 3 | a0001c0001t0002g0224 a0001c0001t0003g0020 a0001c0001t0003g0223 |
4 | HG01069.hp1 HG01243.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.953-11054A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388126 | |||||||
| chr6:55388174 | A | T | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-11006A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388174 | |||||||
| chr6:55388191 | G | A | 1 | a0002c0002t0010g0105 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.953-10989G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388191 | |||||||
| chr6:55388230 | CA | C | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-10942delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55388230 | ||||||
| chr6:55388373 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-10807G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388373 | |||||||
| chr6:55388391 | T | C | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-10789T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388391 | |||||||
| chr6:55388396 | G | T | 1 | a0001c0001t0004g0184 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.953-10784G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388396 | |||||||
| chr6:55388419 | C | G | 3 | a0001c0001t0003g0322 a0001c0001t0003g0323 a0004c0004t0002g0321 |
3 | HG02109.hp2 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.953-10761C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388419 | |||||||
| chr6:55388419 | C | T | 3 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0004g0211 |
3 | HG02559.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.953-10761C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388419 | |||||||
| chr6:55388471 | A | G | 4 | a0004c0004t0002g0030 a0004c0004t0002g0032 a0004c0004t0002g0034 others(1): Show |
7 | HG02080.hp1 NA18969.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.953-10709A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388471 | |||||||
| chr6:55388570 | G | A | 9 | a0001c0005t0003g0226 a0001c0005t0003g0228 a0001c0005t0003g0229 others(6): Show |
10 | HG01884.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.953-10610G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388570 | |||||||
| chr6:55388655 | C | T | 3 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0004g0211 |
3 | HG02559.hp1 HG02647.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.953-10525C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388655 | |||||||
| chr6:55388677 | C | T | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-10503C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388677 | |||||||
| chr6:55388699 | T | C | 1 | a0003c0003t0002g0133 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.953-10481T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388699 | |||||||
| chr6:55388826 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-10354G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388826 | |||||||
| chr6:55388868 | A | G | 3 | a0003c0003t0002g0012 a0003c0003t0002g0116 a0003c0003t0002g0117 |
4 | HG02258.hp2 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.953-10312A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388868 | |||||||
| chr6:55388915 | T | G | 1 | a0003c0003t0002g0243 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.953-10265T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55388915 | |||||||
| chr6:55389222 | T | C | 7 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0003c0003t0002g0056 others(4): Show |
8 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-9958T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389222 | |||||||
| chr6:55389305 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.953-9875A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389305 | |||||||
| chr6:55389391 | C | T | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-9789C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389391 | |||||||
| chr6:55389392 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.953-9788G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389392 | |||||||
| chr6:55389399 | A | T | 1 | a0001c0001t0008g0293 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.953-9781A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389399 | |||||||
| chr6:55389507 | C | G | 1 | a0003c0003t0002g0246 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.953-9673C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389507 | |||||||
| chr6:55389549 | C | CA | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-9624dupA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55389549 | ||||||
| chr6:55389592 | G | C | 1 | a0002c0002t0003g0075 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.953-9588G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389592 | |||||||
| chr6:55389605 | T | C | 21 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-9575T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389605 | |||||||
| chr6:55389606 | C | G | 22 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0003g0247 others(19): Show |
23 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.953-9574C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389606 | |||||||
| chr6:55389772 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.953-9408G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389772 | |||||||
| chr6:55389845 | T | C | 1 | a0003c0003t0002g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.953-9335T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389845 | |||||||
| chr6:55389861 | T | C | 29 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
32 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.953-9319T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389861 | |||||||
| chr6:55389917 | C | G | 21 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0002c0002t0004g0121 others(18): Show |
22 | HG01256.hp2 HG01358.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.953-9263C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55389917 | |||||||
| chr6:55390115 | A | T | 1 | a0003c0003t0002g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.953-9065A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390115 | |||||||
| chr6:55390273 | A | C | 12 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0006g0329 others(9): Show |
13 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.953-8907A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390273 | |||||||
| chr6:55390360 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.953-8820A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390360 | |||||||
| chr6:55390653 | A | G | 10 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0006g0329 others(7): Show |
11 | HG01358.hp1 HG01891.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.953-8527A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390653 | |||||||
| chr6:55390656 | A | G | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.953-8524A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390656 | |||||||
| chr6:55390664 | C | T | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.953-8516C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390664 | |||||||
| chr6:55390705 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.953-8475T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390705 | |||||||
| chr6:55390756 | C | T | 1 | a0003c0003t0002g0237 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.953-8424C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390756 | |||||||
| chr6:55390757 | G | A | 66 | a0001c0001t0003g0205 a0001c0001t0003g0209 a0001c0001t0003g0225 others(63): Show |
73 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.953-8423G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390757 | |||||||
| chr6:55390760 | C | T | 66 | a0001c0001t0003g0205 a0001c0001t0003g0209 a0001c0001t0003g0225 others(63): Show |
73 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.953-8420C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390760 | |||||||
| chr6:55390863 | C | T | 3 | a0001c0001t0003g0193 a0001c0001t0003g0247 a0001c0001t0003g0248 |
3 | HG01891.hp2 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.953-8317C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390863 | |||||||
| chr6:55390867 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.953-8313G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390867 | |||||||
| chr6:55390887 | CACACACA others(1): Show |
C | 4 | a0001c0001t0006g0329 a0001c0001t0011g0040 a0004c0004t0002g0197 others(1): Show |
4 | HG02451.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.953-8285_953-8278d others(10): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55390887 | ||||||
| chr6:55390889 | CACACAT | C | 54 | a0001c0001t0003g0205 a0001c0001t0003g0209 a0001c0001t0003g0225 others(51): Show |
61 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.953-8285_953-8280d others(8): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55390889 | ||||||
| chr6:55390891 | CACAT | C | 10 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0002c0002t0003g0091 others(7): Show |
11 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.953-8285_953-8282d others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55390891 | ||||||
| chr6:55390895 | T | TAC | 61 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(58): Show |
69 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.953-8247_953-8246d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55390895 | ||||||
| chr6:55390895 | T | TACAC | 68 | a0001c0001t0001g0218 a0001c0001t0003g0018 a0001c0001t0004g0009 others(65): Show |
75 | HG00323.hp1 HG00609.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.953-8249_953-8246d others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55390895 | ||||||
| chr6:55390895 | T | TACACAC | 20 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0192 others(17): Show |
23 | HG00099.hp2 HG01074.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.953-8251_953-8246d others(8): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55390895 | ||||||
| chr6:55390895 | T | TACACACA others(1): Show |
16 | a0001c0001t0001g0006 a0001c0001t0001g0214 a0001c0001t0001g0217 others(13): Show |
16 | HG01256.hp1 HG01258.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.953-8253_953-8246d others(10): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55390895 | ||||||
| chr6:55390895 | T | TACACACA others(3): Show |
5 | a0001c0001t0003g0220 a0004c0004t0002g0035 a0004c0004t0002g0325 others(2): Show |
6 | HG01884.hp1 HG02451.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.953-8255_953-8246d others(12): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55390895 | ||||||
| chr6:55390895 | T | TACACACA others(5): Show |
3 | a0003c0003t0002g0160 a0003c0003t0002g0234 a0004c0004t0002g0221 |
3 | HG02647.hp1 HG03831.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.953-8257_953-8246d others(14): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55390895 | ||||||
| chr6:55390895 | TAC | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(55): Show |
68 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.953-8247_953-8246d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55390895 | ||||||
| chr6:55390895 | TACAC | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0046 a0001c0001t0001g0170 others(13): Show |
17 | HG01993.hp1 HG02055.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.953-8249_953-8246d others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55390895 | ||||||
| chr6:55390895 | TACACAC | T | 3 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0181 |
3 | NA18954.hp1 NA19070.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.953-8251_953-8246d others(8): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55390895 | ||||||
| chr6:55390901 | C | T | 10 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0002c0002t0003g0091 others(7): Show |
11 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.953-8279C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390901 | |||||||
| chr6:55390903 | C | T | 55 | a0001c0001t0001g0179 a0001c0001t0003g0205 a0001c0001t0003g0209 others(52): Show |
62 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.953-8277C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390903 | |||||||
| chr6:55390905 | C | T | 4 | a0001c0001t0006g0329 a0001c0001t0011g0040 a0004c0004t0002g0197 others(1): Show |
4 | HG02451.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.953-8275C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390905 | |||||||
| chr6:55390911 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0333 |
2 | NA18946.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.953-8269C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390911 | |||||||
| chr6:55390926 | A | G | 68 | a0001c0001t0003g0205 a0001c0001t0003g0209 a0001c0001t0003g0225 others(65): Show |
76 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.953-8254A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390926 | |||||||
| chr6:55390935 | A | C | 76 | a0001c0001t0003g0205 a0001c0001t0003g0209 a0001c0001t0003g0225 others(73): Show |
84 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.953-8245A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390935 | |||||||
| chr6:55390993 | T | G | 68 | a0001c0001t0003g0205 a0001c0001t0003g0209 a0001c0001t0003g0225 others(65): Show |
76 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.953-8187T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55390993 | |||||||
| chr6:55391003 | T | C | 1 | a0002c0002t0003g0024 | 2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.953-8177T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55391003 | |||||||
| chr6:55391009 | TA | T | 4 | a0001c0001t0006g0329 a0001c0001t0011g0040 a0004c0004t0002g0197 others(1): Show |
4 | HG02451.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.953-8164delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55391009 | ||||||
| chr6:55391030 | A | G | 58 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0037 others(55): Show |
65 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.953-8150A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55391030 | |||||||
| chr6:55391129 | G | A | 68 | a0001c0001t0003g0205 a0001c0001t0003g0209 a0001c0001t0003g0225 others(65): Show |
76 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.953-8051G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55391129 | |||||||
| chr6:55391150 | ACT | A | 46 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0192 others(43): Show |
52 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(49): Show |
intron_variant | MODIFIER | c.953-8029_953-8028d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55391150 | |||||||
| chr6:55391153 | GTTC | G | 8 | a0002c0002t0004g0121 a0002c0002t0004g0135 a0002c0002t0004g0154 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-8024_953-8022d others(5): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55391153 | ||||||
| chr6:55391541 | G | A | 68 | a0001c0001t0003g0205 a0001c0001t0003g0209 a0001c0001t0003g0225 others(65): Show |
76 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.953-7639G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55391541 | |||||||
| chr6:55391576 | G | A | 1 | a0001c0001t0004g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.953-7604G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55391576 | |||||||
| chr6:55391688 | T | C | 56 | a0001c0001t0003g0205 a0001c0001t0003g0209 a0001c0001t0003g0225 others(53): Show |
63 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.953-7492T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55391688 | |||||||
| chr6:55391694 | GA | G | 12 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0006g0329 others(9): Show |
13 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.953-7484delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55391694 | ||||||
| chr6:55391708 | T | C | 68 | a0001c0001t0003g0205 a0001c0001t0003g0209 a0001c0001t0003g0225 others(65): Show |
76 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.953-7472T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55391708 | |||||||
| chr6:55391726 | A | G | 47 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0192 others(44): Show |
53 | HG00099.hp2 HG01074.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.953-7454A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55391726 | |||||||
| chr6:55391743 | A | T | 12 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0006g0329 others(9): Show |
13 | HG01256.hp2 HG01358.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.953-7437A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55391743 | |||||||
| chr6:55391746 | A | T | 2 | a0003c0003t0002g0137 a0003c0003t0002g0138 |
2 | HG00741.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.953-7434A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55391746 | |||||||
| chr6:55391947 | G | T | 1 | a0004c0004t0002g0285 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.953-7233G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55391947 | |||||||
| chr6:55392188 | C | T | 2 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
2 | NA18939.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.953-6992C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392188 | |||||||
| chr6:55392289 | A | C | 1 | a0001c0001t0003g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.953-6891A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392289 | |||||||
| chr6:55392333 | A | G | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.953-6847A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392333 | |||||||
| chr6:55392351 | T | C | 11 | a0001c0001t0006g0329 a0001c0001t0011g0040 a0002c0002t0003g0091 others(8): Show |
11 | HG02055.hp2 HG02109.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.953-6829T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392351 | |||||||
| chr6:55392369 | A | G | 199 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0029 others(196): Show |
226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.953-6811A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392369 | |||||||
| chr6:55392511 | A | G | 76 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0192 others(73): Show |
92 | HG00323.hp1 HG00609.hp1 HG00738.hp1 others(89): Show |
intron_variant | MODIFIER | c.953-6669A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392511 | |||||||
| chr6:55392535 | A | C | 7 | a0001c0005t0004g0021 a0002c0002t0004g0121 a0002c0002t0004g0135 others(4): Show |
8 | HG01891.hp1 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-6645A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392535 | |||||||
| chr6:55392535 | A | G | 77 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0192 others(74): Show |
93 | HG00323.hp1 HG00609.hp1 HG00738.hp1 others(90): Show |
intron_variant | MODIFIER | c.953-6645A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392535 | |||||||
| chr6:55392624 | A | G | 85 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(82): Show |
94 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.953-6556A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392624 | |||||||
| chr6:55392692 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.953-6488T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392692 | |||||||
| chr6:55392712 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.953-6468G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392712 | |||||||
| chr6:55392735 | G | A | 70 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0193 others(67): Show |
79 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.953-6445G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392735 | |||||||
| chr6:55392745 | G | A | 8 | a0001c0001t0003g0020 a0001c0001t0003g0209 a0001c0001t0003g0223 others(5): Show |
10 | HG01069.hp1 HG01243.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.953-6435G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392745 | |||||||
| chr6:55392780 | T | A | 1 | a0003c0003t0002g0152 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.953-6400T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392780 | |||||||
| chr6:55392809 | A | C | 83 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0193 others(80): Show |
92 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.953-6371A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392809 | |||||||
| chr6:55392849 | C | T | 4 | a0004c0004t0002g0206 a0004c0004t0002g0328 a0004c0004t0009g0251 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-6331C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392849 | |||||||
| chr6:55392853 | C | T | 1 | a0002c0002t0001g0058 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.953-6327C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392853 | |||||||
| chr6:55392882 | C | A | 83 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0193 others(80): Show |
92 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.953-6298C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392882 | |||||||
| chr6:55392984 | A | C | 80 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0193 others(77): Show |
89 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.953-6196A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392984 | |||||||
| chr6:55392988 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.953-6192C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55392988 | |||||||
| chr6:55393000 | C | T | 81 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0193 others(78): Show |
90 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.953-6180C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393000 | |||||||
| chr6:55393055 | A | G | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.953-6125A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393055 | |||||||
| chr6:55393137 | C | A | 82 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0193 others(79): Show |
91 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.953-6043C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393137 | |||||||
| chr6:55393138 | A | AT | 69 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0025 others(66): Show |
82 | HG00323.hp1 HG00609.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.953-6038dupT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55393138 | ||||||
| chr6:55393180 | T | A | 1 | a0002c0002t0004g0157 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.953-6000T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393180 | |||||||
| chr6:55393194 | C | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(286): Show |
336 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(333): Show |
intron_variant | MODIFIER | c.953-5986C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393194 | |||||||
| chr6:55393210 | A | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0187 |
3 | HG00609.hp2 NA18961.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.953-5970A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393210 | |||||||
| chr6:55393221 | A | G | 1 | a0001c0001t0004g0274 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.953-5959A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393221 | |||||||
| chr6:55393233 | G | A | 8 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(5): Show |
8 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-5947G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393233 | |||||||
| chr6:55393241 | A | G | 8 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(5): Show |
8 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-5939A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393241 | |||||||
| chr6:55393309 | C | T | 82 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0193 others(79): Show |
91 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.953-5871C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393309 | |||||||
| chr6:55393337 | G | A | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-5843G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393337 | |||||||
| chr6:55393427 | G | A | 83 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0193 others(80): Show |
92 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.953-5753G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393427 | |||||||
| chr6:55393605 | A | G | 8 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(5): Show |
8 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-5575A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393605 | |||||||
| chr6:55393650 | G | A | 15 | a0001c0001t0003g0020 a0001c0001t0003g0193 a0001c0001t0003g0209 others(12): Show |
18 | HG00323.hp2 HG01069.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.953-5530G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393650 | |||||||
| chr6:55393671 | G | A | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.953-5509G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393671 | |||||||
| chr6:55393672 | G | A | 85 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0193 others(82): Show |
94 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.953-5508G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393672 | |||||||
| chr6:55393688 | T | C | 2 | a0003c0003t0002g0114 a0003c0003t0002g0330 |
2 | HG00621.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.953-5492T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393688 | |||||||
| chr6:55393718 | C | T | 82 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0193 others(79): Show |
91 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.953-5462C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393718 | |||||||
| chr6:55393759 | T | C | 8 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(5): Show |
8 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-5421T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393759 | |||||||
| chr6:55393776 | A | G | 48 | a0001c0001t0003g0018 a0001c0001t0003g0205 a0001c0001t0003g0220 others(45): Show |
54 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.953-5404A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393776 | |||||||
| chr6:55393845 | T | A | 120 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0193 others(117): Show |
133 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.953-5335T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393845 | |||||||
| chr6:55393876 | T | C | 82 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0193 others(79): Show |
91 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.953-5304T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55393876 | |||||||
| chr6:55394004 | A | G | 1 | a0003c0003t0002g0110 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.953-5176A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55394004 | |||||||
| chr6:55394089 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.953-5091T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55394089 | |||||||
| chr6:55394313 | G | A | 5 | a0004c0004t0002g0035 a0004c0004t0002g0200 a0004c0004t0002g0321 others(2): Show |
6 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.953-4867G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55394313 | |||||||
| chr6:55394330 | C | A | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.953-4850C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55394330 | |||||||
| chr6:55394339 | T | A | 80 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(77): Show |
88 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.953-4841T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55394339 | |||||||
| chr6:55394520 | A | ATGT | 80 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(77): Show |
88 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.953-4659_953-4657d others(5): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55394520 | ||||||
| chr6:55394709 | A | G | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.953-4471A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55394709 | |||||||
| chr6:55394726 | T | C | 80 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(77): Show |
88 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.953-4454T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55394726 | |||||||
| chr6:55394779 | T | C | 80 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(77): Show |
88 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.953-4401T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55394779 | |||||||
| chr6:55394782 | A | C | 1 | a0002c0002t0003g0069 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.953-4398A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55394782 | |||||||
| chr6:55394818 | A | T | 2 | a0001c0001t0006g0219 a0002c0002t0006g0125 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.953-4362A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55394818 | |||||||
| chr6:55394819 | C | T | 80 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(77): Show |
88 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.953-4361C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55394819 | |||||||
| chr6:55394986 | C | A | 56 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0025 others(53): Show |
65 | HG00323.hp1 HG00609.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.953-4194C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55394986 | |||||||
| chr6:55395053 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.953-4127C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395053 | |||||||
| chr6:55395085 | G | A | 80 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(77): Show |
88 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.953-4095G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395085 | |||||||
| chr6:55395140 | T | C | 80 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(77): Show |
88 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.953-4040T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395140 | |||||||
| chr6:55395162 | G | GA | 10 | a0003c0003t0002g0239 a0004c0004t0002g0035 a0004c0004t0002g0200 others(7): Show |
11 | HG01074.hp2 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.953-4004dupA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395162 | ||||||
| chr6:55395162 | G | GAA | 8 | a0003c0003t0002g0160 a0003c0003t0002g0237 a0003c0003t0002g0240 others(5): Show |
8 | HG00735.hp2 HG02040.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.953-4005_953-4004d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395162 | ||||||
| chr6:55395162 | GA | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0044 others(37): Show |
46 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.953-4004delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395162 | ||||||
| chr6:55395171 | A | AAT | 7 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0270 others(4): Show |
10 | HG00099.hp1 HG00544.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.953-4008_953-4007i others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395171 | ||||||
| chr6:55395171 | A | T | 1 | a0001c0001t0001g0045 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.953-4009A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395171 | |||||||
| chr6:55395173 | A | AATATATA others(5): Show |
2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.953-4006_953-4005i others(14): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395173 | ||||||
| chr6:55395173 | A | AATATATA others(7): Show |
1 | a0001c0005t0003g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.953-4006_953-4005i others(16): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395173 | ||||||
| chr6:55395173 | A | AATATATA others(19): Show |
1 | a0004c0004t0002g0197 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.953-4006_953-4005i others(28): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395173 | ||||||
| chr6:55395173 | A | AT | 7 | a0002c0002t0001g0104 a0002c0002t0001g0108 a0002c0002t0001g0113 others(4): Show |
7 | HG02647.hp1 HG02818.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.953-4007_953-4006i others(3): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395173 | |||||||
| chr6:55395173 | A | ATATATAT others(22): Show |
1 | a0004c0004t0002g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.953-4007_953-4006i others(31): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395173 | |||||||
| chr6:55395173 | A | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(68): Show |
84 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.953-4007A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395173 | |||||||
| chr6:55395175 | A | AAAAAATA others(7): Show |
3 | a0001c0005t0003g0232 a0004c0004t0005g0202 a0004c0004t0005g0203 |
3 | HG02717.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.953-4004_953-4003i others(16): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AAAAAATA others(33): Show |
1 | a0003c0003t0002g0233 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.953-4004_953-4003i others(42): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AAAAATAT others(4): Show |
4 | a0001c0001t0003g0018 a0001c0001t0003g0286 a0002c0002t0003g0003 others(1): Show |
4 | HG01358.hp2 HG01884.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-4004_953-4003i others(13): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AAAAATAT others(6): Show |
2 | a0002c0002t0003g0139 a0004c0004t0005g0204 |
2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.953-4004_953-4003i others(15): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AAAATATA others(3): Show |
1 | a0001c0001t0003g0220 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.953-4004_953-4003i others(12): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AAAATATA others(5): Show |
2 | a0002c0002t0003g0068 a0002c0002t0003g0069 |
2 | HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.953-4004_953-4003i others(14): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AAAATATA others(7): Show |
1 | a0001c0005t0003g0226 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.953-4004_953-4003i others(16): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AAAATATA others(31): Show |
1 | a0003c0003t0002g0141 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.953-4004_953-4003i others(40): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AAATATAT others(2): Show |
6 | a0001c0001t0003g0020 a0002c0002t0003g0065 a0002c0002t0003g0091 others(3): Show |
7 | HG01243.hp2 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.953-4004_953-4003i others(11): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AAATATAT others(4): Show |
27 | a0001c0001t0003g0018 a0001c0001t0003g0314 a0001c0001t0003g0323 others(24): Show |
30 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.953-4004_953-4003i others(13): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AAATATAT others(6): Show |
5 | a0001c0001t0003g0205 a0001c0005t0003g0228 a0002c0002t0003g0003 others(2): Show |
5 | HG03486.hp1 HG03942.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.953-4004_953-4003i others(15): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AATATATA others(3): Show |
1 | a0002c0002t0003g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.953-3995_953-3986d others(12): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AATATATA others(5): Show |
2 | a0002c0002t0003g0073 a0002c0002t0003g0090 |
2 | HG01074.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.953-3997_953-3986d others(14): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AATATATA others(11): Show |
1 | a0002c0002t0003g0075 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.953-4003_953-3986d others(20): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AATATATA others(21): Show |
1 | a0003c0003t0002g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.953-3986_953-3985i others(30): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395175 | A | AT | 3 | a0004c0004t0002g0023 a0004c0004t0002g0201 a0004c0004t0002g0249 |
3 | HG01358.hp1 HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.953-4005_953-4004i others(3): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395175 | |||||||
| chr6:55395175 | A | ATATATAT others(4): Show |
5 | a0001c0001t0003g0210 a0001c0001t0003g0212 a0001c0001t0011g0040 others(2): Show |
5 | HG02451.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.953-4005_953-4004i others(13): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395175 | |||||||
| chr6:55395175 | A | ATATATAT others(6): Show |
4 | a0001c0001t0003g0322 a0001c0005t0003g0229 a0001c0005t0003g0230 others(1): Show |
4 | HG02886.hp2 HG03098.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-4005_953-4004i others(15): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395175 | |||||||
| chr6:55395175 | A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0224 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.953-4005_953-4004i others(19): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395175 | |||||||
| chr6:55395175 | A | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(109): Show |
132 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.953-4005A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395175 | |||||||
| chr6:55395175 | AAT | A | 9 | a0001c0001t0004g0164 a0001c0001t0004g0184 a0002c0002t0003g0236 others(6): Show |
9 | HG00621.hp1 HG02080.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-3987_953-3986d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395175 | ||||||
| chr6:55395176 | AT | A | 59 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0025 others(56): Show |
72 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.953-4003delT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395176 | |||||||
| chr6:55395177 | T | A | 8 | a0001c0001t0004g0027 a0001c0001t0004g0267 a0001c0001t0004g0274 others(5): Show |
9 | HG00738.hp1 HG01074.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.953-4003T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395177 | |||||||
| chr6:55395215 | A | G | 80 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(77): Show |
88 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.953-3965A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395215 | |||||||
| chr6:55395219 | A | G | 80 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(77): Show |
88 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.953-3961A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395219 | |||||||
| chr6:55395325 | G | A | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-3855G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395325 | |||||||
| chr6:55395337 | C | T | 80 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(77): Show |
88 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.953-3843C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395337 | |||||||
| chr6:55395360 | T | C | 48 | a0001c0001t0003g0018 a0001c0001t0003g0205 a0001c0001t0003g0220 others(45): Show |
54 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.953-3820T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395360 | |||||||
| chr6:55395536 | C | T | 2 | a0002c0002t0003g0236 a0006c0006t0003g0258 |
2 | HG02300.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.953-3644C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395536 | |||||||
| chr6:55395558 | G | T | 78 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(75): Show |
86 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.953-3622G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395558 | |||||||
| chr6:55395655 | T | C | 78 | a0001c0001t0002g0224 a0001c0001t0003g0018 a0001c0001t0003g0020 others(75): Show |
86 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.953-3525T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395655 | |||||||
| chr6:55395664 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.953-3516C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395664 | |||||||
| chr6:55395772 | A | G | 2 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
2 | NA18939.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.953-3408A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395772 | |||||||
| chr6:55395781 | G | GA | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(119): Show |
143 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.953-3385dupA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395781 | ||||||
| chr6:55395781 | G | GAA | 44 | a0001c0001t0003g0020 a0001c0001t0003g0209 a0001c0001t0003g0223 others(41): Show |
51 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.953-3386_953-3385d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55395781 | ||||||
| chr6:55395791 | A | AG | 8 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(5): Show |
8 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-3389_953-3388i others(3): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395791 | |||||||
| chr6:55395827 | T | A | 1 | a0003c0003t0002g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.953-3353T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395827 | |||||||
| chr6:55395859 | G | C | 2 | a0003c0003t0002g0141 a0003c0003t0002g0233 |
2 | HG01256.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.953-3321G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395859 | |||||||
| chr6:55395934 | G | A | 1 | a0003c0003t0002g0123 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.953-3246G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395934 | |||||||
| chr6:55395936 | G | T | 5 | a0002c0002t0003g0082 a0002c0002t0003g0091 a0002c0002t0003g0092 others(2): Show |
5 | HG01358.hp2 HG02109.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.953-3244G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395936 | |||||||
| chr6:55395984 | G | A | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-3196G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395984 | |||||||
| chr6:55395997 | T | C | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-3183T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55395997 | |||||||
| chr6:55396008 | G | A | 1 | a0003c0003t0002g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.953-3172G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396008 | |||||||
| chr6:55396010 | C | G | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-3170C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396010 | |||||||
| chr6:55396015 | G | A | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-3165G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396015 | |||||||
| chr6:55396053 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(92): Show |
115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.953-3127T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396053 | |||||||
| chr6:55396065 | G | A | 65 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0025 others(62): Show |
75 | HG00323.hp1 HG00609.hp1 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.953-3115G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396065 | |||||||
| chr6:55396261 | C | T | 7 | a0003c0003t0002g0066 a0003c0003t0002g0130 a0003c0003t0002g0131 others(4): Show |
7 | HG00741.hp1 HG01169.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.953-2919C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396261 | |||||||
| chr6:55396271 | G | A | 25 | a0003c0003t0002g0012 a0003c0003t0002g0022 a0003c0003t0002g0063 others(22): Show |
28 | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.953-2909G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396271 | |||||||
| chr6:55396288 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.953-2892T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396288 | |||||||
| chr6:55396365 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.953-2815T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396365 | |||||||
| chr6:55396514 | G | A | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-2666G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396514 | |||||||
| chr6:55396542 | C | G | 1 | a0004c0004t0002g0030 | 2 | NA18969.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.953-2638C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396542 | |||||||
| chr6:55396543 | C | T | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-2637C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396543 | |||||||
| chr6:55396560 | T | A | 2 | a0001c0001t0004g0184 a0001c0001t0004g0287 |
2 | NA18957.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.953-2620T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396560 | |||||||
| chr6:55396560 | TA | T | 8 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(5): Show |
8 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-2614delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55396560 | ||||||
| chr6:55396561 | A | T | 1 | a0004c0004t0009g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.953-2619A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396561 | |||||||
| chr6:55396599 | G | T | 1 | a0002c0002t0001g0058 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.953-2581G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396599 | |||||||
| chr6:55396626 | A | G | 1 | a0001c0001t0001g0181 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.953-2554A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396626 | |||||||
| chr6:55396769 | T | C | 8 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(5): Show |
8 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.953-2411T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396769 | |||||||
| chr6:55396771 | T | C | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-2409T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396771 | |||||||
| chr6:55396876 | C | CT | 20 | a0001c0001t0001g0187 a0001c0001t0002g0224 a0001c0001t0003g0193 others(17): Show |
24 | HG00544.hp2 HG00558.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.953-2287dupT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55396876 | ||||||
| chr6:55396876 | C | CTTTT | 6 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(3): Show |
6 | HG01256.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.953-2290_953-2287d others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55396876 | ||||||
| chr6:55396876 | CT | C | 7 | a0001c0001t0001g0043 a0002c0002t0003g0067 a0002c0002t0003g0073 others(4): Show |
7 | HG00639.hp2 NA18962.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.953-2287delT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55396876 | ||||||
| chr6:55396984 | T | C | 1 | a0001c0001t0003g0225 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.953-2196T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55396984 | |||||||
| chr6:55397012 | T | A | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-2168T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397012 | |||||||
| chr6:55397055 | T | A | 1 | a0001c0001t0004g0042 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.953-2125T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397055 | |||||||
| chr6:55397159 | C | T | 2 | a0002c0002t0003g0038 a0002c0002t0003g0039 |
2 | NA18939.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.953-2021C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397159 | |||||||
| chr6:55397205 | A | G | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-1975A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397205 | |||||||
| chr6:55397225 | TAAAAAAA others(311): Show |
T | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-1943_953-1626d others(2): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55397225 | ||||||
| chr6:55397226 | A | T | 51 | a0001c0001t0003g0018 a0001c0001t0003g0205 a0001c0001t0003g0220 others(48): Show |
58 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.953-1954A>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397226 | |||||||
| chr6:55397240 | C | T | 1 | a0003c0003t0002g0136 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.953-1940C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397240 | |||||||
| chr6:55397284 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.953-1896C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397284 | |||||||
| chr6:55397311 | G | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(92): Show |
115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.953-1869G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397311 | |||||||
| chr6:55397313 | T | G | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.953-1867T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397313 | |||||||
| chr6:55397381 | A | G | 1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-1799A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397381 | |||||||
| chr6:55397386 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.953-1794C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397386 | |||||||
| chr6:55397419 | G | C | 1 | a0003c0003t0002g0004 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.953-1761G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397419 | |||||||
| chr6:55397449 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.953-1731C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397449 | |||||||
| chr6:55397493 | C | T | 1 | a0004c0004t0002g0023 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.953-1687C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397493 | |||||||
| chr6:55397524 | C | CA | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(111): Show |
130 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.953-1630dupA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55397524 | ||||||
| chr6:55397524 | C | CAA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(83): Show |
94 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.953-1631_953-1630d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55397524 | ||||||
| chr6:55397524 | C | CAAA | 23 | a0001c0001t0001g0005 a0001c0001t0001g0168 a0001c0001t0001g0171 others(20): Show |
24 | HG00738.hp1 HG01081.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.953-1632_953-1630d others(5): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55397524 | ||||||
| chr6:55397524 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.953-1641_953-1630d others(14): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55397524 | ||||||
| chr6:55397524 | C | CAAAAAAA others(16): Show |
1 | a0006c0006t0003g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.953-1652_953-1630d others(25): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55397524 | ||||||
| chr6:55397524 | C | CAAAAAAA others(20): Show |
1 | a0002c0002t0003g0236 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.953-1630_953-1629i others(29): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55397524 | ||||||
| chr6:55397524 | CA | C | 32 | a0001c0001t0003g0220 a0001c0001t0003g0286 a0002c0002t0003g0003 others(29): Show |
35 | HG00408.hp2 HG00642.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.953-1630delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55397524 | ||||||
| chr6:55397524 | CAA | C | 12 | a0001c0001t0003g0018 a0001c0001t0003g0205 a0001c0001t0003g0322 others(9): Show |
13 | HG01884.hp2 HG02109.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.953-1631_953-1630d others(4): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55397524 | ||||||
| chr6:55397524 | CAAAA | C | 9 | a0001c0001t0003g0193 a0001c0001t0003g0210 a0001c0001t0003g0212 others(6): Show |
9 | HG01358.hp2 HG01891.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-1633_953-1630d others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55397524 | ||||||
| chr6:55397524 | CAAAAA | C | 12 | a0001c0001t0003g0020 a0001c0001t0003g0209 a0001c0001t0003g0223 others(9): Show |
14 | HG01069.hp1 HG01243.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.953-1634_953-1630d others(7): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55397524 | ||||||
| chr6:55397577 | T | C | 10 | a0001c0001t0003g0207 a0003c0003t0002g0141 a0003c0003t0002g0143 others(7): Show |
10 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.953-1603T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397577 | |||||||
| chr6:55397609 | C | T | 1 | a0001c0001t0003g0018 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.953-1571C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397609 | |||||||
| chr6:55397735 | C | T | 10 | a0001c0001t0003g0205 a0001c0001t0003g0322 a0001c0005t0003g0226 others(7): Show |
10 | HG02886.hp2 HG02922.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.953-1445C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397735 | |||||||
| chr6:55397767 | A | G | 49 | a0003c0003t0002g0004 a0003c0003t0002g0013 a0003c0003t0002g0066 others(46): Show |
57 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.953-1413A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397767 | |||||||
| chr6:55397797 | C | G | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-1383C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397797 | |||||||
| chr6:55397850 | A | AT | 4 | a0003c0003t0002g0057 a0003c0003t0002g0256 a0004c0004t0002g0201 others(1): Show |
4 | HG02647.hp1 HG02976.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-1330_953-1329i others(3): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397850 | |||||||
| chr6:55397851 | C | G | 4 | a0003c0003t0002g0057 a0003c0003t0002g0256 a0004c0004t0002g0201 others(1): Show |
4 | HG02647.hp1 HG02976.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-1329C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397851 | |||||||
| chr6:55397884 | C | T | 3 | a0003c0003t0002g0056 a0004c0004t0002g0023 a0004c0004t0002g0249 |
4 | HG01358.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.953-1296C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397884 | |||||||
| chr6:55397887 | AT | A | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-1287delT | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55397887 | ||||||
| chr6:55397891 | T | G | 1 | a0004c0004t0002g0249 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.953-1289T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397891 | |||||||
| chr6:55397900 | T | A | 1 | a0004c0004t0002g0221 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.953-1280T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55397900 | |||||||
| chr6:55398007 | A | G | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-1173A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398007 | |||||||
| chr6:55398312 | C | A | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-868C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398312 | |||||||
| chr6:55398365 | C | G | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.953-815C>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398365 | |||||||
| chr6:55398369 | T | TTTAACC | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-809_953-808ins others(6): Show |
GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 55398369 | ||||||
| chr6:55398382 | A | G | 1 | a0003c0003t0002g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.953-798A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398382 | |||||||
| chr6:55398426 | A | C | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-754A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398426 | |||||||
| chr6:55398442 | C | T | 3 | a0003c0003t0002g0056 a0004c0004t0002g0023 a0004c0004t0002g0249 |
4 | HG01358.hp1 HG02630.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.953-738C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398442 | |||||||
| chr6:55398443 | G | A | 2 | a0002c0002t0003g0082 a0002c0002t0003g0120 |
2 | HG01358.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.953-737G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398443 | |||||||
| chr6:55398504 | G | T | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-676G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398504 | |||||||
| chr6:55398526 | G | T | 2 | a0001c0001t0004g0290 a0001c0001t0004g0291 |
2 | HG01175.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.953-654G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398526 | |||||||
| chr6:55398589 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(92): Show |
115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.953-591G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398589 | |||||||
| chr6:55398614 | A | G | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-566A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398614 | |||||||
| chr6:55398634 | G | C | 1 | a0004c0004t0002g0299 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.953-546G>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398634 | |||||||
| chr6:55398659 | T | C | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-521T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398659 | |||||||
| chr6:55398676 | A | G | 9 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(6): Show |
9 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-504A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398676 | |||||||
| chr6:55398734 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.953-446T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398734 | |||||||
| chr6:55398835 | T | C | 3 | a0004c0004t0005g0202 a0004c0004t0005g0203 a0004c0004t0005g0204 |
3 | HG02258.hp1 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.953-345T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398835 | |||||||
| chr6:55398898 | G | A | 4 | a0001c0001t0003g0314 a0002c0002t0003g0088 a0002c0002t0003g0089 others(1): Show |
4 | HG00642.hp1 HG01074.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-282G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398898 | |||||||
| chr6:55398982 | C | T | 1 | a0002c0002t0004g0106 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.953-198C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398982 | |||||||
| chr6:55398991 | C | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(239): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.953-189C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55398991 | |||||||
| chr6:55399123 | T | C | 4 | a0001c0001t0003g0314 a0002c0002t0003g0088 a0002c0002t0003g0089 others(1): Show |
4 | HG00642.hp1 HG01074.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-57T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 6/8 | chr6 | 55399123 | |||||||
| chr6:55399478 | G | T | 1 | a0003c0003t0002g0056 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1121+37G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55399478 | |||||||
| chr6:55399564 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1121+123T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55399564 | |||||||
| chr6:55399663 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(230): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1121+222C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55399663 | |||||||
| chr6:55399695 | A | G | 5 | a0001c0001t0004g0184 a0001c0001t0004g0287 a0001c0001t0004g0302 others(2): Show |
5 | HG00609.hp1 NA18957.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+254A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55399695 | |||||||
| chr6:55399710 | A | G | 1 | a0003c0003t0002g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1121+269A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55399710 | |||||||
| chr6:55399733 | C | T | 8 | a0003c0003t0002g0141 a0003c0003t0002g0143 a0003c0003t0002g0233 others(5): Show |
8 | HG01256.hp2 HG02258.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1121+292C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55399733 | |||||||
| chr6:55399909 | A | C | 2 | a0002c0002t0003g0236 a0006c0006t0003g0258 |
2 | HG02300.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1121+468A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55399909 | |||||||
| chr6:55400035 | G | A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0323 |
3 | HG01884.hp2 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1121+594G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400035 | |||||||
| chr6:55400153 | TA | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(229): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1121+720delA | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 55400153 | ||||||
| chr6:55400166 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(230): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1121+725C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400166 | |||||||
| chr6:55400223 | A | G | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1121+782A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400223 | |||||||
| chr6:55400230 | T | A | 1 | a0001c0001t0003g0323 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1121+789T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400230 | |||||||
| chr6:55400344 | G | T | 1 | a0001c0001t0003g0018 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1121+903G>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400344 | |||||||
| chr6:55400352 | T | A | 1 | a0002c0002t0004g0156 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1121+911T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400352 | |||||||
| chr6:55400352 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(92): Show |
115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1121+911T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400352 | |||||||
| chr6:55400498 | G | A | 3 | a0004c0004t0002g0206 a0004c0004t0002g0328 a0005c0009t0002g0250 |
3 | HG02055.hp2 HG02257.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1121+1057G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400498 | |||||||
| chr6:55400502 | G | A | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1121+1061G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400502 | |||||||
| chr6:55400528 | C | T | 4 | a0003c0003t0002g0012 a0003c0003t0002g0116 a0003c0003t0002g0117 others(1): Show |
5 | HG02145.hp1 HG02258.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+1087C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400528 | |||||||
| chr6:55400572 | C | A | 1 | a0003c0003t0002g0127 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1121+1131C>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400572 | |||||||
| chr6:55400596 | C | T | 1 | a0003c0003t0002g0142 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1121+1155C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400596 | |||||||
| chr6:55400599 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(230): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1121+1158T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400599 | |||||||
| chr6:55400662 | AG | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(230): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1122-1126delG | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 55400662 | ||||||
| chr6:55400665 | C | T | 2 | a0002c0002t0003g0236 a0006c0006t0003g0258 |
2 | HG02300.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1122-1125C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400665 | |||||||
| chr6:55400699 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(230): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1122-1091G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400699 | |||||||
| chr6:55400717 | G | A | 2 | a0002c0002t0003g0236 a0006c0006t0003g0258 |
2 | HG02300.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1122-1073G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400717 | |||||||
| chr6:55400826 | T | G | 2 | a0003c0003t0002g0243 a0003c0003t0002g0244 |
2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1122-964T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400826 | |||||||
| chr6:55400891 | G | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(230): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1122-899G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400891 | |||||||
| chr6:55400922 | T | G | 47 | a0001c0001t0003g0018 a0001c0001t0003g0205 a0001c0001t0003g0220 others(44): Show |
53 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1122-868T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400922 | |||||||
| chr6:55400948 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(231): Show |
272 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.1122-842T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400948 | |||||||
| chr6:55400994 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(230): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1122-796C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55400994 | |||||||
| chr6:55401060 | G | A | 2 | a0002c0002t0003g0236 a0006c0006t0003g0258 |
2 | HG02300.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1122-730G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401060 | |||||||
| chr6:55401116 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(166): Show |
197 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1122-674A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401116 | |||||||
| chr6:55401126 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1122-664T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401126 | |||||||
| chr6:55401144 | T | G | 4 | a0003c0003t0002g0022 a0003c0003t0002g0063 a0003c0003t0002g0234 others(1): Show |
5 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1122-646T>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401144 | |||||||
| chr6:55401178 | T | C | 16 | a0001c0001t0003g0020 a0001c0001t0003g0193 a0001c0001t0003g0209 others(13): Show |
18 | HG01069.hp1 HG01243.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1122-612T>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401178 | |||||||
| chr6:55401295 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1122-495C>T | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401295 | |||||||
| chr6:55401336 | A | C | 1 | a0004c0004t0002g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1122-454A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401336 | |||||||
| chr6:55401344 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(92): Show |
115 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1122-446G>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401344 | |||||||
| chr6:55401364 | A | G | 2 | a0002c0002t0003g0236 a0006c0006t0003g0258 |
2 | HG02300.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1122-426A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401364 | |||||||
| chr6:55401509 | A | C | 1 | a0001c0001t0004g0268 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1122-281A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401509 | |||||||
| chr6:55401525 | A | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(229): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.1122-265A>C | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401525 | |||||||
| chr6:55401563 | A | G | 1 | a0001c0001t0003g0207 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1122-227A>G | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401563 | |||||||
| chr6:55401596 | T | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(230): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.1122-194T>A | GFRAL | ENSG00000187871.2 | transcript | ENST00000340465.2 | protein_coding | 8/8 | chr6 | 55401596 |