Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9810 |
| ensemblid | ENSG00000103549.22 |
| hgncid | 16867 |
| symbol | RNF40 |
| name | ring finger protein 40 |
| refseq_nuc | NM_014771.4 |
| refseq_prot | NP_055586.1 |
| ensembl_nuc | ENST00000324685.11 |
| ensembl_prot | ENSP00000325677.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 30762322 |
| end | 30776307 |
| strand | + |
| ver | v1.2 |
| region | chr16:30762322-30776307 |
| region5000 | chr16:30757322-30781307 |
| regionname0 | RNF40_chr16_30762322_30776307 |
| regionname5000 | RNF40_chr16_30757322_30781307 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1001 | 228 | 70 | 58 | 62 | 12 | 24 | 39 | RNF40_chr16_30757322_30781307 | RNF40 | MSGPG others(996): Show |
chr16 | 30757322 | 30781307 |
| a0002 | 0/0 | 1001 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | MSGPG others(996): Show |
chr16 | 30757322 | 30781307 |
| a0003 | 0/0 | 1001 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF40_chr16_30757322_30781307 | RNF40 | MSGPG others(996): Show |
chr16 | 30757322 | 30781307 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3003 | 214 | 61 | 55 | 61 | 12 | 24 | RNF40_chr16_30757322_30781307 | RNF40 | ATGTC others(2998): Show |
chr16 | 30757322 | 30781307 | ||
| a0001c0002 | 1/0 | 3003 | 6 | 4 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | ATGTC others(2998): Show |
chr16 | 30757322 | 30781307 | ||
| a0001c0003 | 0/0 | 3003 | 2 | 2 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | ATGTC others(2998): Show |
chr16 | 30757322 | 30781307 | ||
| a0001c0004 | 0/0 | 3003 | 2 | 1 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | ATGTC others(2998): Show |
chr16 | 30757322 | 30781307 | ||
| a0001c0006 | 0/0 | 3003 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | ATGTC others(2998): Show |
chr16 | 30757322 | 30781307 | ||
| a0001c0008 | 0/0 | 3003 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | ATGTC others(2998): Show |
chr16 | 30757322 | 30781307 | ||
| a0001c0009 | 0/0 | 3003 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | ATGTC others(2998): Show |
chr16 | 30757322 | 30781307 | ||
| a0001c0010 | 0/0 | 3003 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | ATGTC others(2998): Show |
chr16 | 30757322 | 30781307 | ||
| a0002c0005 | 0/0 | 3003 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | ATGTC others(2998): Show |
chr16 | 30757322 | 30781307 | ||
| a0003c0007 | 0/0 | 3003 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | ATGTC others(2998): Show |
chr16 | 30757322 | 30781307 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5309 | 99 | 43 | 16 | 19 | 4 | 17 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0002 | 0/1 | 5309 | 87 | 4 | 31 | 39 | 5 | 7 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0003 | 0/0 | 5309 | 9 | 1 | 6 | 0 | 2 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0004 | 0/0 | 5309 | 2 | 2 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0005 | 0/0 | 5308 | 4 | 4 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5303): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0006 | 0/0 | 5309 | 3 | 3 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0008 | 0/0 | 5309 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0009 | 0/0 | 5309 | 1 | 0 | 0 | 0 | 1 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0010 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0011 | 0/0 | 5309 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0012 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0013 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0014 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0015 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0016 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0001t0017 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0002t0004 | 1/0 | 5309 | 6 | 4 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0003t0001 | 0/0 | 5309 | 2 | 2 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0004t0007 | 0/0 | 5309 | 2 | 1 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0006t0003 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0008t0002 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0009t0003 | 0/0 | 5309 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0001c0010t0001 | 0/0 | 5309 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0002c0005t0002 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| a0003c0007t0002 | 0/0 | 5309 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | GAAAT others(5304): Show |
chr16 | 30757322 | 30781307 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 49 | 19 | 7 | 13 | 2 | 8 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0003 | 0/0 | 11 | 4 | 2 | 1 | 0 | 4 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0001 | 0/0 | 23 | 2 | 9 | 9 | 1 | 2 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0002 | 0/1 | 38 | 2 | 13 | 15 | 2 | 5 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0003g0004 | 0/0 | 7 | 0 | 5 | 0 | 2 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0005g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0006g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0008g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0009g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0013g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0014g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0015g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0016g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0001t0017g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0002t0004g0005 | 1/0 | 5 | 3 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0004t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0004t0007g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0006t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0008t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0009t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0001c0010t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0002c0005t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| a0003c0007t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0057 | EUR | FIN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00323 | hp1 | a0001 | c0001 | t0009 | g0001 | EUR | FIN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00408 | hp1 | a0001 | c0008 | t0002 | g0001 | EAS | CHS | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00609 | hp2 | a0002 | c0005 | t0002 | g0002 | EAS | CHS | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01256 | hp2 | a0001 | c0001 | t0011 | g0002 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01346 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01496 | hp1 | a0001 | c0004 | t0007 | g0029 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01884 | hp1 | a0001 | c0006 | t0003 | g0002 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0050 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0035 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01891 | hp2 | a0001 | c0001 | t0017 | g0011 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0001 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02257 | hp2 | a0001 | c0010 | t0001 | g0001 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02300 | hp1 | a0001 | c0009 | t0003 | g0025 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02809 | hp1 | a0001 | c0002 | t0004 | g0005 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02896 | hp1 | a0001 | c0004 | t0007 | g0019 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03225 | hp1 | a0001 | c0001 | t0013 | g0002 | AFR | MSL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03486 | hp1 | a0001 | c0001 | t0016 | g0014 | AFR | MSL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0056 | AFR | ESN | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03579 | hp2 | a0001 | c0002 | t0004 | g0005 | AFR | MSL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18747 | hp2 | a0001 | c0001 | t0015 | g0015 | EAS | CHB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | YRI | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0005 | AFR | YRI | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18974 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19011 | hp2 | a0003 | c0007 | t0002 | g0023 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | LWK | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19059 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19079 | hp2 | a0001 | c0001 | t0014 | g0002 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | YRI | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0042 | EUR | TSI | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | USA | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | USA | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0009 | AFR | LWK | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0002 | REF | REF | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0004 | g0005 | REF | REF | RNF40_chr16_30757322_30781307 | RNF40 | chr16 | 30757322 | 30781307 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30764371 | G | A | 1 | a0002 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.635G>A | p.Arg212Gln | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 5/20 | 745/5309 | 635/3006 | 212/1001 | chr16 | 30764371 | |||
| chr16:30768857 | G | A | 1 | a0003 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.2117G>A | p.Arg706His | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 15/20 | 2227/5309 | 2117/3006 | 706/1001 | chr16 | 30768857 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30762650 | C | T | 1 | a0001c0010 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.105C>T | p.Pro35Pro | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 2/20 | 215/5309 | 105/3006 | 35/1001 | chr16 | 30762650 | |||
| chr16:30764363 | C | T | 1 | a0001c0009 | 1 | HG02300.hp1 | synonymous_variant | LOW | c.627C>T | p.Leu209Leu | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 5/20 | 737/5309 | 627/3006 | 209/1001 | chr16 | 30764363 | |||
| chr16:30765210 | G | A | 1 | a0001c0003 | 2 | HG01891.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.801G>A | p.Ser267Ser | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 7/20 | 911/5309 | 801/3006 | 267/1001 | chr16 | 30765210 | |||
| chr16:30766210 | C | T | 1 | a0001c0008 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.1041C>T | p.Asn347Asn | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 9/20 | 1151/5309 | 1041/3006 | 347/1001 | chr16 | 30766210 | |||
| chr16:30766420 | G | A | 1 | a0001c0006 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.1155G>A | p.Thr385Thr | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 10/20 | 1265/5309 | 1155/3006 | 385/1001 | chr16 | 30766420 | |||
| chr16:30769507 | A | G | 9 | a0001c0001 a0001c0003 a0001c0004 others(6): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
synonymous_variant | LOW | c.2493A>G | p.Leu831Leu | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/20 | 2603/5309 | 2493/3006 | 831/1001 | chr16 | 30769507 | |||
| chr16:30772145 | C | T | 1 | a0001c0004 | 2 | HG01496.hp1 HG02896.hp1 |
synonymous_variant | LOW | c.2784C>T | p.Tyr928Tyr | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 19/20 | 2894/5309 | 2784/3006 | 928/1001 | chr16 | 30772145 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30762501 | T | C | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(17): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-45T>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 2/20 | chr16 | 30762501 | |||||||
| chr16:30762517 | G | C | 1 | a0001c0001t0008 | 1 | HG01346.hp2 | 5_prime_UTR_variant | MODIFIER | c.-29G>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 2/20 | 29 | chr16 | 30762517 | ||||||
| chr16:30774146 | G | A | 1 | a0001c0001t0009 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*32G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 32 | chr16 | 30774146 | ||||||
| chr16:30774494 | C | T | 1 | a0001c0001t0015 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*380C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 380 | chr16 | 30774494 | ||||||
| chr16:30774503 | C | T | 5 | a0001c0001t0003 a0001c0001t0005 a0001c0004t0007 others(2): Show |
17 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*389C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 389 | chr16 | 30774503 | ||||||
| chr16:30774863 | TG | T | 1 | a0001c0001t0005 | 4 | HG02145.hp1 HG03540.hp2 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*752delG | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 752 | INFO_REALIGN_3_PRIME | chr16 | 30774863 | |||||
| chr16:30775056 | G | A | 1 | a0001c0001t0010 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*942G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 942 | chr16 | 30775056 | ||||||
| chr16:30775250 | A | G | 1 | a0001c0001t0014 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1136A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 1136 | chr16 | 30775250 | ||||||
| chr16:30775346 | C | G | 1 | a0001c0001t0017 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1232C>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 1232 | chr16 | 30775346 | ||||||
| chr16:30775362 | G | A | 1 | a0001c0001t0011 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1248G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 1248 | chr16 | 30775362 | ||||||
| chr16:30775394 | T | C | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(19): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*1280T>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 1280 | chr16 | 30775394 | ||||||
| chr16:30775606 | C | T | 4 | a0001c0001t0001 a0001c0001t0013 a0001c0003t0001 others(1): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*1492C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 1492 | chr16 | 30775606 | ||||||
| chr16:30775841 | C | A | 1 | a0001c0001t0016 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1727C>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 1727 | chr16 | 30775841 | ||||||
| chr16:30775990 | G | C | 1 | a0001c0001t0012 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1876G>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 1876 | chr16 | 30775990 | ||||||
| chr16:30776119 | G | A | 1 | a0001c0001t0013 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2005G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 2005 | chr16 | 30776119 | ||||||
| chr16:30776237 | G | A | 2 | a0001c0001t0005 a0001c0004t0007 |
6 | HG01496.hp1 HG02145.hp1 HG02896.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2123G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 20/20 | 2123 | chr16 | 30776237 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:30762397 | A | G | 1 | a0001c0001t0002g0061 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-72+37A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 1/19 | chr16 | 30762397 | |||||||
| chr16:30764545 | G | T | 1 | a0001c0001t0003g0060 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.649+160G>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 5/19 | chr16 | 30764545 | |||||||
| chr16:30764611 | T | C | 1 | a0001c0004t0007g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.649+226T>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 5/19 | chr16 | 30764611 | |||||||
| chr16:30764666 | C | T | 1 | a0001c0001t0002g0059 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.650-272C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 5/19 | chr16 | 30764666 | |||||||
| chr16:30764864 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.650-74G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 5/19 | chr16 | 30764864 | |||||||
| chr16:30765509 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.993+10G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 8/19 | chr16 | 30765509 | |||||||
| chr16:30765562 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0015g0015 |
3 | NA18747.hp2 NA18960.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.993+63C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 8/19 | chr16 | 30765562 | |||||||
| chr16:30765700 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.993+201A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 8/19 | chr16 | 30765700 | |||||||
| chr16:30765733 | A | G | 1 | a0001c0001t0001g0018 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.993+234A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 8/19 | chr16 | 30765733 | |||||||
| chr16:30766343 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1114-36C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 9/19 | chr16 | 30766343 | |||||||
| chr16:30766615 | C | T | 1 | a0001c0002t0004g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1293+57C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 10/19 | chr16 | 30766615 | |||||||
| chr16:30766932 | G | A | 1 | a0001c0001t0001g0022 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1429+56G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 11/19 | chr16 | 30766932 | |||||||
| chr16:30767007 | A | C | 1 | a0001c0001t0002g0055 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1429+131A>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 11/19 | chr16 | 30767007 | |||||||
| chr16:30767036 | A | G | 2 | a0001c0001t0006g0014 a0001c0001t0016g0014 |
3 | HG02280.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1429+160A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 11/19 | chr16 | 30767036 | |||||||
| chr16:30767324 | G | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.1429+448G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 11/19 | chr16 | 30767324 | |||||||
| chr16:30767356 | A | G | 1 | a0001c0001t0001g0013 | 3 | HG02109.hp1 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1429+480A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 11/19 | chr16 | 30767356 | |||||||
| chr16:30767431 | T | C | 1 | a0003c0007t0002g0023 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1430-463T>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 11/19 | chr16 | 30767431 | |||||||
| chr16:30767477 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0017 |
5 | HG00140.hp1 HG01081.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.1430-417C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 11/19 | chr16 | 30767477 | |||||||
| chr16:30767487 | G | A | 4 | a0001c0001t0003g0004 a0001c0001t0003g0024 a0001c0001t0003g0060 others(1): Show |
10 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1430-407G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 11/19 | chr16 | 30767487 | |||||||
| chr16:30767773 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1430-121A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 11/19 | chr16 | 30767773 | |||||||
| chr16:30767782 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0017 |
5 | HG00140.hp1 HG01081.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.1430-112T>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 11/19 | chr16 | 30767782 | |||||||
| chr16:30769168 | T | G | 1 | a0001c0001t0001g0016 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2248-18T>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 15/19 | chr16 | 30769168 | |||||||
| chr16:30769621 | C | G | 1 | a0001c0001t0002g0053 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2586+21C>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30769621 | |||||||
| chr16:30769659 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2586+59G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30769659 | |||||||
| chr16:30769673 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG00140.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.2586+73C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30769673 | |||||||
| chr16:30769824 | G | A | 2 | a0001c0001t0005g0009 a0001c0001t0005g0027 |
4 | HG02145.hp1 HG03540.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.2586+224G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30769824 | |||||||
| chr16:30769869 | G | A | 1 | a0001c0001t0001g0006 | 4 | HG00673.hp1 NA18747.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.2586+269G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30769869 | |||||||
| chr16:30769874 | G | T | 1 | a0001c0001t0002g0052 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2586+274G>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30769874 | |||||||
| chr16:30769932 | T | C | 1 | a0001c0001t0002g0028 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2586+332T>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30769932 | |||||||
| chr16:30770115 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2586+515A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770115 | |||||||
| chr16:30770119 | A | ATGGATTT others(12): Show |
2 | a0001c0004t0007g0019 a0001c0004t0007g0029 |
2 | HG01496.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.2586+520_2586+521i others(21): Show |
RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr16 | 30770119 | ||||||
| chr16:30770119 | A | ATGGATTT others(13): Show |
6 | a0001c0001t0001g0016 a0001c0001t0002g0030 a0001c0001t0003g0004 others(3): Show |
15 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.2586+520_2586+521i others(22): Show |
RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr16 | 30770119 | ||||||
| chr16:30770119 | A | ATGGATTT others(14): Show |
36 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(33): Show |
82 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.2586+520_2586+521i others(23): Show |
RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr16 | 30770119 | ||||||
| chr16:30770119 | A | ATGGATTT others(15): Show |
19 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0010 others(16): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.2586+520_2586+521i others(24): Show |
RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr16 | 30770119 | ||||||
| chr16:30770119 | A | ATGGATTT others(16): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0047 others(3): Show |
17 | HG00741.hp2 HG01106.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.2586+520_2586+521i others(25): Show |
RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr16 | 30770119 | ||||||
| chr16:30770119 | A | ATGGATTT others(17): Show |
2 | a0001c0001t0001g0054 a0001c0001t0002g0049 |
2 | HG01928.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.2586+520_2586+521i others(26): Show |
RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr16 | 30770119 | ||||||
| chr16:30770149 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2586+549C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770149 | |||||||
| chr16:30770176 | G | A | 1 | a0001c0001t0002g0031 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2586+576G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770176 | |||||||
| chr16:30770190 | T | C | 1 | a0001c0001t0002g0032 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2586+590T>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770190 | |||||||
| chr16:30770193 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2586+593G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770193 | |||||||
| chr16:30770266 | C | T | 1 | a0001c0001t0002g0042 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2586+666C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770266 | |||||||
| chr16:30770428 | G | A | 1 | a0001c0001t0002g0034 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2586+828G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770428 | |||||||
| chr16:30770621 | A | G | 4 | a0001c0001t0003g0004 a0001c0001t0003g0024 a0001c0001t0003g0060 others(1): Show |
10 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.2586+1021A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770621 | |||||||
| chr16:30770640 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2586+1040T>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770640 | |||||||
| chr16:30770691 | T | C | 1 | a0001c0003t0001g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2586+1091T>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770691 | |||||||
| chr16:30770752 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2587-1081C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770752 | |||||||
| chr16:30770774 | C | A | 1 | a0001c0002t0004g0056 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2587-1059C>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770774 | |||||||
| chr16:30770924 | C | T | 1 | a0001c0001t0002g0055 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2587-909C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770924 | |||||||
| chr16:30770970 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(68): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2587-863A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30770970 | |||||||
| chr16:30771035 | C | T | 1 | a0001c0001t0002g0041 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2587-798C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30771035 | |||||||
| chr16:30771128 | G | A | 4 | a0001c0001t0003g0004 a0001c0001t0003g0024 a0001c0001t0003g0060 others(1): Show |
10 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.2587-705G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30771128 | |||||||
| chr16:30771320 | C | G | 1 | a0001c0001t0001g0013 | 3 | HG02109.hp1 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2587-513C>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30771320 | |||||||
| chr16:30771399 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(68): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2587-434T>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30771399 | |||||||
| chr16:30771434 | G | A | 1 | a0001c0001t0003g0024 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2587-399G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30771434 | |||||||
| chr16:30771494 | A | G | 1 | a0001c0001t0002g0040 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2587-339A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30771494 | |||||||
| chr16:30771627 | AAAAC | A | 4 | a0001c0001t0003g0004 a0001c0001t0003g0024 a0001c0001t0003g0060 others(1): Show |
10 | HG00099.hp1 HG00140.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.2587-202_2587-199d others(6): Show |
RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr16 | 30771627 | ||||||
| chr16:30771631 | CAAAG | C | 2 | a0001c0001t0004g0011 a0001c0001t0017g0011 |
3 | HG01891.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2587-198_2587-195d others(6): Show |
RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr16 | 30771631 | ||||||
| chr16:30771704 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2587-129C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 17/19 | chr16 | 30771704 | |||||||
| chr16:30772019 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2727+46G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 18/19 | chr16 | 30772019 | |||||||
| chr16:30772039 | C | T | 3 | a0001c0001t0001g0008 a0001c0003t0001g0035 a0001c0003t0001g0045 |
6 | HG01891.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2728-50C>T | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 18/19 | chr16 | 30772039 | |||||||
| chr16:30772341 | G | C | 1 | a0001c0001t0002g0036 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2829+151G>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 19/19 | chr16 | 30772341 | |||||||
| chr16:30772478 | A | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(2): Show |
13 | HG01891.hp1 HG02280.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2829+288A>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 19/19 | chr16 | 30772478 | |||||||
| chr16:30772526 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2829+336T>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 19/19 | chr16 | 30772526 | |||||||
| chr16:30772599 | G | A | 1 | a0001c0001t0006g0050 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2829+409G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 19/19 | chr16 | 30772599 | |||||||
| chr16:30772656 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(68): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.2829+466G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 19/19 | chr16 | 30772656 | |||||||
| chr16:30772690 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0047 |
3 | HG00280.hp2 HG00741.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.2829+500G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 19/19 | chr16 | 30772690 | |||||||
| chr16:30772728 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2829+538G>A | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 19/19 | chr16 | 30772728 | |||||||
| chr16:30772783 | CAGG | C | 2 | a0001c0001t0006g0014 a0001c0001t0016g0014 |
3 | HG02280.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2829+596_2829+598d others(5): Show |
RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr16 | 30772783 | ||||||
| chr16:30773598 | A | C | 1 | a0001c0001t0002g0039 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2830-340A>C | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 19/19 | chr16 | 30773598 | |||||||
| chr16:30773734 | A | G | 2 | a0001c0001t0006g0014 a0001c0001t0016g0014 |
3 | HG02280.hp1 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2830-204A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 19/19 | chr16 | 30773734 | |||||||
| chr16:30773786 | A | G | 1 | a0001c0001t0002g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2830-152A>G | RNF40 | ENSG00000103549.22 | transcript | ENST00000324685.11 | protein_coding | 19/19 | chr16 | 30773786 |