Item | Value |
---|---|
geneid | 65008 |
ensemblid | ENSG00000169288.18 |
hgncid | 14275 |
symbol | MRPL1 |
name | mitochondrial ribosomal protein L1 |
refseq_nuc | NM_020236.4 |
refseq_prot | NP_064621.3 |
ensembl_nuc | ENST00000315567.13 |
ensembl_prot | ENSP00000315017.8 |
mane_status | MANE Select |
chr | chr4 |
start | 77862830 |
end | 77952785 |
strand | + |
ver | v1.2 |
region | chr4:77862830-77952785 |
region5000 | chr4:77857830-77957785 |
regionname0 | MRPL1_chr4_77862830_77952785 |
regionname5000 | MRPL1_chr4_77857830_77957785 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 325 | 292 | 74 | 46 | 133 | 8 | 29 | 107 | MRPL1_chr4_77857830_77957785 | MRPL1 | MAAAV others(320): Show |
chr4 | 77857830 | 77957785 |
a0002 | 0/0 | 325 | 9 | 4 | 2 | 0 | 0 | 3 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | MAAAV others(320): Show |
chr4 | 77857830 | 77957785 |
a0003 | 0/0 | 325 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | MAAAV others(320): Show |
chr4 | 77857830 | 77957785 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 975 | 283 | 73 | 45 | 130 | 7 | 26 | MRPL1_chr4_77857830_77957785 | MRPL1 | ATGGC others(970): Show |
chr4 | 77857830 | 77957785 | ||
a0001c0003 | 0/0 | 975 | 5 | 1 | 1 | 0 | 1 | 2 | MRPL1_chr4_77857830_77957785 | MRPL1 | ATGGC others(970): Show |
chr4 | 77857830 | 77957785 | ||
a0001c0004 | 0/0 | 975 | 3 | 0 | 0 | 3 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | ATGGC others(970): Show |
chr4 | 77857830 | 77957785 | ||
a0001c0005 | 0/0 | 975 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | ATGGC others(970): Show |
chr4 | 77857830 | 77957785 | ||
a0002c0002 | 0/0 | 975 | 9 | 4 | 2 | 0 | 0 | 3 | MRPL1_chr4_77857830_77957785 | MRPL1 | ATGGC others(970): Show |
chr4 | 77857830 | 77957785 | ||
a0003c0006 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | ATGGC others(970): Show |
chr4 | 77857830 | 77957785 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1175 | 271 | 61 | 45 | 130 | 7 | 26 | MRPL1_chr4_77857830_77957785 | MRPL1 | GCAAT others(1170): Show |
chr4 | 77857830 | 77957785 |
a0001c0001t0002 | 0/0 | 1175 | 12 | 12 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | GCAAT others(1170): Show |
chr4 | 77857830 | 77957785 |
a0001c0003t0001 | 0/0 | 1175 | 5 | 1 | 1 | 0 | 1 | 2 | MRPL1_chr4_77857830_77957785 | MRPL1 | GCAAT others(1170): Show |
chr4 | 77857830 | 77957785 |
a0001c0004t0001 | 0/0 | 1175 | 3 | 0 | 0 | 3 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | GCAAT others(1170): Show |
chr4 | 77857830 | 77957785 |
a0001c0005t0001 | 0/0 | 1175 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | GCAAT others(1170): Show |
chr4 | 77857830 | 77957785 |
a0002c0002t0002 | 0/0 | 1175 | 9 | 4 | 2 | 0 | 0 | 3 | MRPL1_chr4_77857830_77957785 | MRPL1 | GCAAT others(1170): Show |
chr4 | 77857830 | 77957785 |
a0003c0006t0001 | 0/0 | 1175 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | GCAAT others(1170): Show |
chr4 | 77857830 | 77957785 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0002 | 0/1 | 3 | 0 | 2 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0001c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0002c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
a0003c0006t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0066 | EUR | GBR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | FIN | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00438 | hp1 | a0001 | c0004 | t0001 | g0194 | EAS | CHS | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0089 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0068 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0085 | AMR | CLM | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01891 | hp1 | a0002 | c0002 | t0002 | g0088 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0074 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0090 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02738 | hp1 | a0001 | c0003 | t0001 | g0072 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ESN | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | ESN | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ESN | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0087 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03453 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0065 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | STU | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | STU | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | BEB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | STU | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0093 | SAS | STU | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0091 | SAS | STU | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG04204 | hp2 | a0001 | c0005 | t0001 | g0133 | SAS | STU | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | YRI | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18747 | hp2 | a0001 | c0004 | t0001 | g0203 | EAS | CHB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18952 | hp1 | a0001 | c0004 | t0001 | g0206 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18968 | hp2 | a0003 | c0006 | t0001 | g0201 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ASW | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ASW | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | TSI | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | TSI | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | GIH | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | USA | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | USA | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | USA | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | USA | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0002 | REF | REF | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0223 | REF | REF | MRPL1_chr4_77857830_77957785 | MRPL1 | chr4 | 77857830 | 77957785 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:77909280 | G | C | 1 | a0002 | 9 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
missense_variant | MODERATE | c.685G>C | p.Asp229His | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/9 | 704/1175 | 685/978 | 229/325 | chr4 | 77909280 | |||
chr4:77949867 | C | G | 1 | a0003 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.848C>G | p.Pro283Arg | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/9 | 867/1175 | 848/978 | 283/325 | chr4 | 77949867 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:77883320 | A | G | 1 | a0001c0004 | 3 | HG00438.hp1 NA18747.hp2 NA18952.hp1 |
synonymous_variant | LOW | c.222A>G | p.Ala74Ala | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/9 | 241/1175 | 222/978 | 74/325 | chr4 | 77883320 | |||
chr4:77883431 | T | C | 1 | a0001c0005 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.333T>C | p.Ile111Ile | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/9 | 352/1175 | 333/978 | 111/325 | chr4 | 77883431 | |||
chr4:77885261 | C | T | 1 | a0001c0003 | 5 | HG00099.hp2 HG00741.hp2 HG02257.hp2 others(2): Show |
synonymous_variant | LOW | c.408C>T | p.Asn136Asn | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/9 | 427/1175 | 408/978 | 136/325 | chr4 | 77885261 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:77952669 | A | T | 2 | a0001c0001t0002 a0002c0002t0002 |
21 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*62A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 9/9 | 62 | chr4 | 77952669 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:77862972 | A | C | 1 | a0001c0001t0001g0282 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.31+93A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77862972 | |||||||
chr4:77863107 | A | T | 1 | a0001c0001t0001g0281 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.31+228A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77863107 | |||||||
chr4:77863139 | C | G | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.31+260C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77863139 | |||||||
chr4:77863279 | T | A | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.31+400T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77863279 | |||||||
chr4:77863279 | T | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(77): Show |
81 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.31+400T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77863279 | |||||||
chr4:77863447 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.31+568T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77863447 | |||||||
chr4:77863461 | A | AT | 32 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0250 others(29): Show |
35 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.31+603dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863461 | A | ATTTTTT | 24 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
24 | HG02004.hp1 HG02129.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.31+598_31+603dupTT others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863461 | A | ATTTTTTT | 17 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(14): Show |
17 | HG00673.hp2 HG01109.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.31+597_31+603dupTT others(5): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863461 | A | ATTTTTTT others(1): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0064 others(8): Show |
12 | HG00099.hp2 HG00741.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.31+596_31+603dupTT others(6): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863461 | A | ATTTTTTT others(2): Show |
8 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0076 others(5): Show |
8 | HG02145.hp2 HG02257.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.31+595_31+603dupTT others(7): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863461 | A | ATTTTTTT others(3): Show |
3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0002g0082 |
3 | HG02258.hp1 HG02965.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.31+594_31+603dupTT others(8): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863461 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0002g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31+592_31+603dupTT others(10): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863461 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0001g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.31+590_31+603dupTT others(12): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863461 | A | ATTTTTTT others(17): Show |
1 | a0002c0002t0002g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.31+603_31+604insTT others(22): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863461 | A | ATTTTTTT others(18): Show |
6 | a0002c0002t0002g0086 a0002c0002t0002g0087 a0002c0002t0002g0088 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.31+603_31+604insTT others(23): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863461 | A | ATTTTTTT others(19): Show |
2 | a0002c0002t0002g0092 a0002c0002t0002g0093 |
2 | HG02809.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.31+603_31+604insTT others(24): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863461 | A | ATTTTTTT others(20): Show |
1 | a0001c0001t0002g0094 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.31+603_31+604insTT others(25): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863461 | A | ATTTTTTT others(25): Show |
1 | a0001c0001t0002g0095 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.31+603_31+604insTT others(30): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77863461 | ||||||
chr4:77863470 | T | G | 6 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG02258.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.31+591T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77863470 | |||||||
chr4:77863483 | G | C | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.31+604G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77863483 | |||||||
chr4:77863491 | A | C | 1 | a0001c0001t0002g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31+612A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77863491 | |||||||
chr4:77863894 | C | T | 28 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0228 others(25): Show |
30 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.31+1015C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77863894 | |||||||
chr4:77863926 | A | G | 10 | a0001c0001t0002g0082 a0002c0002t0002g0085 a0002c0002t0002g0086 others(7): Show |
10 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+1047A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77863926 | |||||||
chr4:77864000 | GT | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(116): Show |
129 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.31+1140delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77864000 | ||||||
chr4:77864000 | GTT | G | 69 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(66): Show |
71 | HG00099.hp2 HG00673.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.31+1139_31+1140del others(2): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77864000 | ||||||
chr4:77864000 | GTTT | G | 10 | a0001c0001t0001g0022 a0001c0001t0002g0082 a0001c0001t0002g0083 others(7): Show |
10 | HG01891.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+1138_31+1140del others(3): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77864000 | ||||||
chr4:77864164 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.31+1285G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864164 | |||||||
chr4:77864580 | A | G | 121 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.31+1701A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864580 | |||||||
chr4:77864612 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.31+1733C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864612 | |||||||
chr4:77864658 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.31+1779C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864658 | |||||||
chr4:77864663 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.31+1784C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864663 | |||||||
chr4:77864689 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.31+1810C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864689 | |||||||
chr4:77864700 | C | T | 2 | a0002c0002t0002g0091 a0002c0002t0002g0093 |
2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.31+1821C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864700 | |||||||
chr4:77864800 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31+1921A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864800 | |||||||
chr4:77864871 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.31+1992G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864871 | |||||||
chr4:77864886 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.31+2007A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864886 | |||||||
chr4:77864890 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.31+2011C>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864890 | |||||||
chr4:77864890 | C | CT | 76 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(73): Show |
77 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.31+2029dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77864890 | ||||||
chr4:77864953 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.31+2074C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864953 | |||||||
chr4:77864969 | A | C | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.31+2090A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864969 | |||||||
chr4:77864984 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.31+2105G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77864984 | |||||||
chr4:77865035 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.31+2156G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77865035 | |||||||
chr4:77865071 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.31+2192G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77865071 | |||||||
chr4:77865180 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.31+2301A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77865180 | |||||||
chr4:77865238 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.31+2359G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77865238 | |||||||
chr4:77865427 | C | CT | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.31+2560dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77865427 | ||||||
chr4:77865450 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.31+2571C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77865450 | |||||||
chr4:77865490 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.31+2611C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77865490 | |||||||
chr4:77865534 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.31+2655A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77865534 | |||||||
chr4:77865536 | T | A | 12 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0114 others(9): Show |
16 | HG01993.hp1 HG02083.hp2 HG02293.hp1 others(13): Show |
intron_variant | MODIFIER | c.31+2657T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77865536 | |||||||
chr4:77865536 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.31+2657T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77865536 | |||||||
chr4:77865664 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.31+2785G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77865664 | |||||||
chr4:77865692 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.31+2813A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77865692 | |||||||
chr4:77866038 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.31+3159C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77866038 | |||||||
chr4:77866225 | T | G | 1 | a0001c0001t0001g0122 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.31+3346T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77866225 | |||||||
chr4:77866345 | C | G | 1 | a0001c0001t0001g0277 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.31+3466C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77866345 | |||||||
chr4:77866426 | A | G | 1 | a0001c0003t0001g0068 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.31+3547A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77866426 | |||||||
chr4:77866428 | C | T | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.31+3549C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77866428 | |||||||
chr4:77866549 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.31+3670G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77866549 | |||||||
chr4:77866611 | G | A | 10 | a0001c0001t0002g0082 a0002c0002t0002g0085 a0002c0002t0002g0086 others(7): Show |
10 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+3732G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77866611 | |||||||
chr4:77866699 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.31+3820G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77866699 | |||||||
chr4:77866748 | C | CT | 7 | a0001c0001t0001g0067 a0001c0001t0001g0084 a0001c0001t0002g0019 others(4): Show |
7 | HG02451.hp1 HG02922.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+3869_31+3870ins others(1): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77866748 | |||||||
chr4:77866749 | C | T | 80 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(77): Show |
81 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.31+3870C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77866749 | |||||||
chr4:77866750 | T | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(6): Show |
12 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.31+3871T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77866750 | |||||||
chr4:77866915 | T | C | 4 | a0001c0001t0001g0125 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | NA18968.hp1 NA18999.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.31+4036T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77866915 | |||||||
chr4:77867014 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.31+4135G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77867014 | |||||||
chr4:77867120 | A | G | 5 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0083 others(2): Show |
5 | HG02280.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+4241A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77867120 | |||||||
chr4:77867454 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.32-4290A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77867454 | |||||||
chr4:77867470 | A | G | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.32-4274A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77867470 | |||||||
chr4:77867530 | C | CTTTTCT | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0117 others(8): Show |
14 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.32-4192_32-4187dup others(6): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77867530 | ||||||
chr4:77867542 | TTTTTCTT others(4): Show |
T | 1 | a0001c0001t0002g0082 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.32-4192_32-4182del others(11): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77867542 | ||||||
chr4:77867542 | TTTTTCTT others(9): Show |
T | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.32-4193_32-4178del others(16): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77867542 | ||||||
chr4:77867548 | TTTTTC | T | 77 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(74): Show |
78 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.32-4182_32-4178del others(5): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77867548 | ||||||
chr4:77867573 | A | G | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.32-4171A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77867573 | |||||||
chr4:77867746 | C | CT | 65 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0022 others(62): Show |
66 | HG00099.hp2 HG00741.hp2 HG01109.hp2 others(63): Show |
intron_variant | MODIFIER | c.32-3969dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77867746 | ||||||
chr4:77867746 | C | CTT | 14 | a0001c0001t0001g0018 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
14 | HG00673.hp2 HG00738.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.32-3970_32-3969dup others(2): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77867746 | ||||||
chr4:77867746 | CT | C | 25 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0112 others(22): Show |
26 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.32-3969delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77867746 | ||||||
chr4:77867746 | CTT | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0107 others(6): Show |
10 | HG00735.hp1 HG01256.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.32-3970_32-3969del others(2): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77867746 | ||||||
chr4:77867746 | CTTTTTTT others(1): Show |
C | 72 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(69): Show |
77 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.32-3976_32-3969del others(8): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77867746 | ||||||
chr4:77867746 | CTTTTTTT others(2): Show |
C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0102 a0001c0001t0001g0103 others(5): Show |
9 | HG02145.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.32-3977_32-3969del others(9): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77867746 | ||||||
chr4:77867746 | CTTTTTTT others(4): Show |
C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.32-3979_32-3969del others(11): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77867746 | ||||||
chr4:77867779 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.32-3965C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77867779 | |||||||
chr4:77867861 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.32-3883G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77867861 | |||||||
chr4:77867946 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.32-3798C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77867946 | |||||||
chr4:77867949 | G | T | 10 | a0001c0001t0002g0082 a0002c0002t0002g0085 a0002c0002t0002g0086 others(7): Show |
10 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.32-3795G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77867949 | |||||||
chr4:77867974 | T | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(194): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.32-3770T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77867974 | |||||||
chr4:77868012 | C | T | 4 | a0001c0001t0001g0125 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | NA18968.hp1 NA18999.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.32-3732C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868012 | |||||||
chr4:77868074 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.32-3670T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868074 | |||||||
chr4:77868098 | T | C | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.32-3646T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868098 | |||||||
chr4:77868170 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.32-3574T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868170 | |||||||
chr4:77868329 | A | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.32-3415A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868329 | |||||||
chr4:77868445 | G | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.32-3299G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868445 | |||||||
chr4:77868518 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.32-3226G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868518 | |||||||
chr4:77868536 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.32-3208C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868536 | |||||||
chr4:77868645 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.32-3099C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868645 | |||||||
chr4:77868646 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.32-3098T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868646 | |||||||
chr4:77868694 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.32-3050C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868694 | |||||||
chr4:77868753 | A | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0069 a0001c0001t0001g0070 others(6): Show |
10 | HG03490.hp2 HG03491.hp2 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.32-2991A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868753 | |||||||
chr4:77868870 | G | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02922.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.32-2874G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868870 | |||||||
chr4:77868874 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.32-2870G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77868874 | |||||||
chr4:77869151 | G | A | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.32-2593G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77869151 | |||||||
chr4:77869160 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.32-2584G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77869160 | |||||||
chr4:77869511 | T | C | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.32-2233T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77869511 | |||||||
chr4:77869580 | G | GTTGT | 3 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0002c0002t0002g0088 |
3 | HG01071.hp1 HG01071.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.32-2137_32-2134dup others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77869580 | ||||||
chr4:77869580 | GTTGT | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(69): Show |
73 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.32-2137_32-2134del others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77869580 | ||||||
chr4:77869580 | GTTGTTTG others(5): Show |
G | 1 | a0001c0001t0001g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.32-2145_32-2134del others(12): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77869580 | ||||||
chr4:77869625 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.32-2119C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77869625 | |||||||
chr4:77869846 | T | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.32-1898T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77869846 | |||||||
chr4:77870389 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.32-1355A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77870389 | |||||||
chr4:77870451 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.32-1293T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77870451 | |||||||
chr4:77871102 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.32-642C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77871102 | |||||||
chr4:77871287 | A | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.32-457A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77871287 | |||||||
chr4:77871303 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.32-441T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77871303 | |||||||
chr4:77871308 | CT | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.32-422delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | 77871308 | ||||||
chr4:77871344 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(59): Show |
63 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.32-400G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77871344 | |||||||
chr4:77871452 | G | A | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.32-292G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77871452 | |||||||
chr4:77871505 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.32-239C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77871505 | |||||||
chr4:77871506 | G | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0102 others(12): Show |
17 | HG00735.hp1 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.32-238G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77871506 | |||||||
chr4:77871589 | A | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.32-155A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77871589 | |||||||
chr4:77871593 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.32-151T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 1/8 | chr4 | 77871593 | |||||||
chr4:77871982 | A | T | 1 | a0001c0001t0001g0275 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.143+127A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77871982 | |||||||
chr4:77872104 | A | T | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.143+249A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77872104 | |||||||
chr4:77872184 | G | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.143+329G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77872184 | |||||||
chr4:77872295 | A | AAATT | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.143+445_143+448dup others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 77872295 | ||||||
chr4:77872314 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.143+459C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77872314 | |||||||
chr4:77872379 | C | T | 6 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG02258.hp2 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.143+524C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77872379 | |||||||
chr4:77872551 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.143+696G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77872551 | |||||||
chr4:77872720 | G | A | 95 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.143+865G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77872720 | |||||||
chr4:77872799 | G | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.143+944G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77872799 | |||||||
chr4:77872818 | G | T | 1 | a0001c0001t0001g0175 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.143+963G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77872818 | |||||||
chr4:77872843 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.143+988A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77872843 | |||||||
chr4:77872906 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.143+1051A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77872906 | |||||||
chr4:77873200 | G | A | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.143+1345G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77873200 | |||||||
chr4:77873302 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.143+1447A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77873302 | |||||||
chr4:77873365 | G | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.143+1510G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77873365 | |||||||
chr4:77873387 | T | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.143+1532T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77873387 | |||||||
chr4:77873530 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0078 |
2 | NA18950.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.143+1675A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77873530 | |||||||
chr4:77873924 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.143+2069A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77873924 | |||||||
chr4:77874001 | C | CT | 6 | a0001c0001t0001g0177 a0001c0001t0001g0230 a0001c0001t0001g0231 others(3): Show |
6 | HG00639.hp1 HG01071.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.143+2161dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 77874001 | ||||||
chr4:77874029 | T | C | 4 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0094 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.143+2174T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77874029 | |||||||
chr4:77874276 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0002g0019 a0001c0001t0002g0020 |
3 | HG02451.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.143+2421G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77874276 | |||||||
chr4:77874287 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.143+2432G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77874287 | |||||||
chr4:77874406 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.143+2551A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77874406 | |||||||
chr4:77874438 | T | C | 33 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0022 others(30): Show |
33 | HG00673.hp2 HG01928.hp1 HG02004.hp1 others(30): Show |
intron_variant | MODIFIER | c.143+2583T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77874438 | |||||||
chr4:77874442 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.143+2587A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77874442 | |||||||
chr4:77874782 | CT | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.143+2943delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 77874782 | ||||||
chr4:77874838 | A | G | 16 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0002g0021 others(13): Show |
16 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.143+2983A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77874838 | |||||||
chr4:77875068 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.143+3213G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875068 | |||||||
chr4:77875077 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.143+3222C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875077 | |||||||
chr4:77875078 | A | G | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.143+3223A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875078 | |||||||
chr4:77875085 | G | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0212 |
2 | NA18980.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.143+3230G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875085 | |||||||
chr4:77875138 | T | G | 1 | a0001c0001t0001g0079 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.143+3283T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875138 | |||||||
chr4:77875171 | T | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0080 |
3 | HG02145.hp2 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.143+3316T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875171 | |||||||
chr4:77875314 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.143+3459G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875314 | |||||||
chr4:77875541 | A | G | 79 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(76): Show |
80 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.143+3686A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875541 | |||||||
chr4:77875552 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.143+3697T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875552 | |||||||
chr4:77875658 | A | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0270 |
2 | HG03688.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.143+3803A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875658 | |||||||
chr4:77875694 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.143+3839G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875694 | |||||||
chr4:77875805 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.143+3950G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875805 | |||||||
chr4:77875923 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.143+4068C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77875923 | |||||||
chr4:77876118 | G | C | 10 | a0001c0001t0002g0082 a0002c0002t0002g0085 a0002c0002t0002g0086 others(7): Show |
10 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.143+4263G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77876118 | |||||||
chr4:77876150 | T | A | 1 | a0001c0001t0001g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.143+4295T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77876150 | |||||||
chr4:77876179 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(59): Show |
63 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.143+4324G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77876179 | |||||||
chr4:77876231 | C | T | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.143+4376C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77876231 | |||||||
chr4:77876261 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.143+4406C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77876261 | |||||||
chr4:77876460 | A | C | 1 | a0001c0003t0001g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.143+4605A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77876460 | |||||||
chr4:77876706 | A | G | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(203): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.143+4851A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77876706 | |||||||
chr4:77876734 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA18940.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.143+4879T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77876734 | |||||||
chr4:77876909 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.143+5054A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77876909 | |||||||
chr4:77877045 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.143+5190C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77877045 | |||||||
chr4:77877282 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.143+5427G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77877282 | |||||||
chr4:77877316 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.143+5461G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77877316 | |||||||
chr4:77877447 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.143+5592G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77877447 | |||||||
chr4:77877494 | T | C | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(202): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.143+5639T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77877494 | |||||||
chr4:77877589 | A | AT | 64 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0022 others(61): Show |
65 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.144-5633dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 77877589 | ||||||
chr4:77877589 | A | ATT | 9 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0042 others(6): Show |
9 | HG02145.hp2 HG02451.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-5634_144-5633d others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 77877589 | ||||||
chr4:77877589 | AT | A | 9 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0106 others(6): Show |
9 | HG01256.hp1 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-5633delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 77877589 | ||||||
chr4:77877762 | T | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.144-5480T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77877762 | |||||||
chr4:77877863 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.144-5379C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77877863 | |||||||
chr4:77878015 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.144-5227C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77878015 | |||||||
chr4:77878116 | A | C | 1 | a0001c0001t0001g0025 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.144-5126A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77878116 | |||||||
chr4:77878226 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.144-5016G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77878226 | |||||||
chr4:77878245 | A | G | 5 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | NA18944.hp1 NA18978.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.144-4997A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77878245 | |||||||
chr4:77878255 | C | T | 9 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0035 others(6): Show |
9 | NA18945.hp2 NA18957.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-4987C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77878255 | |||||||
chr4:77878402 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.144-4840C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77878402 | |||||||
chr4:77878638 | G | C | 1 | a0001c0001t0001g0183 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.144-4604G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77878638 | |||||||
chr4:77878793 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.144-4449C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77878793 | |||||||
chr4:77878810 | C | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.144-4432C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77878810 | |||||||
chr4:77878833 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.144-4409C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77878833 | |||||||
chr4:77878955 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.144-4287G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77878955 | |||||||
chr4:77878979 | G | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02922.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.144-4263G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77878979 | |||||||
chr4:77879128 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.144-4114A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77879128 | |||||||
chr4:77879456 | T | C | 1 | a0001c0001t0002g0082 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.144-3786T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77879456 | |||||||
chr4:77879600 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0081 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.144-3642G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77879600 | |||||||
chr4:77879716 | A | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0228 others(11): Show |
16 | HG00280.hp1 HG01071.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.144-3526A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77879716 | |||||||
chr4:77879917 | G | C | 3 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0002g0234 |
3 | HG02970.hp2 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.144-3325G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77879917 | |||||||
chr4:77879926 | T | G | 1 | a0001c0001t0001g0167 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.144-3316T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77879926 | |||||||
chr4:77879934 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.144-3308G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77879934 | |||||||
chr4:77879990 | G | T | 1 | a0001c0004t0001g0206 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.144-3252G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77879990 | |||||||
chr4:77880204 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.144-3038G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77880204 | |||||||
chr4:77880218 | A | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.144-3024A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77880218 | |||||||
chr4:77880235 | G | A | 121 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.144-3007G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77880235 | |||||||
chr4:77880435 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.144-2807G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77880435 | |||||||
chr4:77880495 | C | CT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0100 a0001c0001t0001g0108 others(18): Show |
22 | HG00735.hp1 HG01255.hp2 HG02293.hp2 others(19): Show |
intron_variant | MODIFIER | c.144-2730dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 77880495 | ||||||
chr4:77880495 | CT | C | 17 | a0001c0001t0001g0114 a0001c0001t0002g0019 a0001c0001t0002g0020 others(14): Show |
17 | HG00099.hp2 HG00639.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.144-2730delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 77880495 | ||||||
chr4:77880495 | CTT | C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(62): Show |
66 | HG00673.hp2 HG01109.hp2 HG01928.hp1 others(63): Show |
intron_variant | MODIFIER | c.144-2731_144-2730d others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 77880495 | ||||||
chr4:77880533 | C | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(75): Show |
79 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.144-2709C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77880533 | |||||||
chr4:77880787 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.144-2455A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77880787 | |||||||
chr4:77880832 | A | G | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.144-2410A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77880832 | |||||||
chr4:77881141 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.144-2101A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77881141 | |||||||
chr4:77881212 | T | C | 11 | a0001c0001t0001g0232 a0001c0001t0001g0236 a0001c0001t0001g0237 others(8): Show |
11 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.144-2030T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77881212 | |||||||
chr4:77881421 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.144-1821C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77881421 | |||||||
chr4:77881443 | C | CT | 8 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0033 others(5): Show |
9 | HG00639.hp1 HG00735.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.144-1780dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 77881443 | ||||||
chr4:77881443 | C | CTT | 14 | a0001c0001t0001g0084 a0001c0001t0001g0124 a0001c0001t0002g0021 others(11): Show |
14 | HG01496.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.144-1781_144-1780d others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 77881443 | ||||||
chr4:77881443 | CT | C | 6 | a0001c0001t0001g0046 a0001c0001t0001g0079 a0001c0001t0001g0158 others(3): Show |
6 | HG00323.hp1 HG01255.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-1780delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | 77881443 | ||||||
chr4:77881568 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.144-1674A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77881568 | |||||||
chr4:77881596 | T | C | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.144-1646T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77881596 | |||||||
chr4:77881764 | C | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0124 a0001c0001t0002g0083 |
3 | HG03453.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.144-1478C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77881764 | |||||||
chr4:77881879 | T | G | 1 | a0001c0001t0001g0027 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.144-1363T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77881879 | |||||||
chr4:77882072 | A | G | 10 | a0001c0001t0002g0082 a0002c0002t0002g0085 a0002c0002t0002g0086 others(7): Show |
10 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.144-1170A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77882072 | |||||||
chr4:77882110 | G | A | 79 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(76): Show |
80 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.144-1132G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77882110 | |||||||
chr4:77882131 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.144-1111A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77882131 | |||||||
chr4:77882258 | A | G | 1 | a0002c0002t0002g0089 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.144-984A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77882258 | |||||||
chr4:77882804 | A | G | 4 | a0001c0001t0001g0125 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | NA18968.hp1 NA18999.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-438A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77882804 | |||||||
chr4:77882817 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.144-425T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77882817 | |||||||
chr4:77882884 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.144-358C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77882884 | |||||||
chr4:77882891 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.144-351T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77882891 | |||||||
chr4:77882984 | G | C | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.144-258G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77882984 | |||||||
chr4:77883011 | A | C | 2 | a0001c0001t0001g0235 a0001c0001t0002g0234 |
2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.144-231A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77883011 | |||||||
chr4:77883083 | C | G | 121 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.144-159C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77883083 | |||||||
chr4:77883086 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.144-156G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77883086 | |||||||
chr4:77883186 | T | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0102 others(12): Show |
17 | HG00735.hp1 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.144-56T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77883186 | |||||||
chr4:77883187 | A | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(63): Show |
67 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.144-55A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77883187 | |||||||
chr4:77883188 | A | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.144-54A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77883188 | |||||||
chr4:77883189 | A | T | 62 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(59): Show |
63 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.144-53A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77883189 | |||||||
chr4:77883198 | C | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0176 |
3 | HG02083.hp2 NA18945.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.144-44C>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77883198 | |||||||
chr4:77883203 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.144-39G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 2/8 | chr4 | 77883203 | |||||||
chr4:77883852 | A | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.402+352A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77883852 | |||||||
chr4:77883877 | C | T | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.402+377C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77883877 | |||||||
chr4:77883900 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0177 |
2 | NA18967.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.402+400C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77883900 | |||||||
chr4:77883908 | A | T | 1 | a0001c0001t0001g0248 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.402+408A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77883908 | |||||||
chr4:77883909 | T | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0213 |
2 | HG00544.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.402+409T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77883909 | |||||||
chr4:77883992 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0152 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.402+492G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77883992 | |||||||
chr4:77884028 | A | G | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.402+528A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77884028 | |||||||
chr4:77884114 | T | C | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.402+614T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77884114 | |||||||
chr4:77884134 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0107 others(6): Show |
10 | HG00735.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.402+634T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77884134 | |||||||
chr4:77884156 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.402+656G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77884156 | |||||||
chr4:77884200 | G | C | 1 | a0001c0004t0001g0206 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.402+700G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77884200 | |||||||
chr4:77884244 | C | CA | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0051 others(16): Show |
21 | HG00735.hp1 HG01243.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.402+760dupA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 77884244 | ||||||
chr4:77884244 | CA | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0126 a0001c0001t0001g0204 others(4): Show |
7 | HG01169.hp1 HG02015.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.402+760delA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 77884244 | ||||||
chr4:77884269 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.402+769G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77884269 | |||||||
chr4:77884318 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.402+818A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77884318 | |||||||
chr4:77884410 | T | G | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.403-846T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77884410 | |||||||
chr4:77884503 | A | C | 1 | a0001c0001t0001g0231 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.403-753A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77884503 | |||||||
chr4:77884822 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.403-434G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77884822 | |||||||
chr4:77884888 | G | C | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.403-368G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77884888 | |||||||
chr4:77884999 | G | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG02922.hp1 HG02970.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.403-257G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77884999 | |||||||
chr4:77885053 | A | C | 1 | a0001c0001t0001g0175 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.403-203A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77885053 | |||||||
chr4:77885085 | GATGAATA others(7): Show |
G | 1 | a0001c0001t0001g0186 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.403-158_403-145del others(14): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | 77885085 | ||||||
chr4:77885099 | C | A | 96 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(93): Show |
102 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.403-157C>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 3/8 | chr4 | 77885099 | |||||||
chr4:77885353 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.486+14G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77885353 | |||||||
chr4:77885525 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.486+186C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77885525 | |||||||
chr4:77885552 | A | G | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.486+213A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77885552 | |||||||
chr4:77885559 | T | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.486+220T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77885559 | |||||||
chr4:77885577 | G | T | 1 | a0001c0001t0001g0211 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.486+238G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77885577 | |||||||
chr4:77885608 | G | A | 2 | a0001c0001t0001g0148 a0002c0002t0002g0086 |
2 | HG03453.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.486+269G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77885608 | |||||||
chr4:77885868 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.486+529A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77885868 | |||||||
chr4:77886204 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.486+865T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77886204 | |||||||
chr4:77886449 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0069 a0001c0001t0001g0070 others(6): Show |
10 | HG03490.hp2 HG03491.hp2 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.487-771C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77886449 | |||||||
chr4:77886522 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.487-698C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77886522 | |||||||
chr4:77886608 | C | T | 1 | a0001c0004t0001g0203 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.487-612C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77886608 | |||||||
chr4:77886744 | A | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(75): Show |
79 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.487-476A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77886744 | |||||||
chr4:77886789 | C | CT | 41 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(38): Show |
44 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.487-410dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 77886789 | ||||||
chr4:77886789 | C | CTT | 55 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(52): Show |
58 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.487-411_487-410dup others(2): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 77886789 | ||||||
chr4:77886789 | C | CTTT | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0146 others(14): Show |
19 | HG00280.hp1 HG01071.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.487-412_487-410dup others(3): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 77886789 | ||||||
chr4:77886789 | CT | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0022 others(68): Show |
72 | HG00099.hp2 HG00323.hp2 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.487-410delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr4 | 77886789 | ||||||
chr4:77886794 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0226 |
2 | NA19004.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.487-426T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77886794 | |||||||
chr4:77886950 | G | A | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.487-270G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77886950 | |||||||
chr4:77886979 | G | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0154 others(8): Show |
12 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(9): Show |
intron_variant | MODIFIER | c.487-241G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 4/8 | chr4 | 77886979 | |||||||
chr4:77887391 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.558+100G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77887391 | |||||||
chr4:77887391 | G | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.558+100G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77887391 | |||||||
chr4:77887513 | G | GGT | 3 | a0001c0001t0001g0122 a0001c0001t0002g0019 a0001c0001t0002g0020 |
3 | HG02451.hp1 HG03540.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.558+239_558+240dup others(2): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 77887513 | ||||||
chr4:77887515 | T | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(75): Show |
79 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.558+224T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77887515 | |||||||
chr4:77887590 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.558+299A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77887590 | |||||||
chr4:77887884 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.558+593C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77887884 | |||||||
chr4:77887949 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.558+658T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77887949 | |||||||
chr4:77888019 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.558+728T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77888019 | |||||||
chr4:77888223 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.558+932C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77888223 | |||||||
chr4:77888230 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.558+939C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77888230 | |||||||
chr4:77888375 | C | T | 17 | a0001c0001t0001g0084 a0001c0001t0002g0019 a0001c0001t0002g0020 others(14): Show |
17 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.558+1084C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77888375 | |||||||
chr4:77888428 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.558+1137C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77888428 | |||||||
chr4:77888498 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.558+1207G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77888498 | |||||||
chr4:77888500 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0041 |
2 | NA18985.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.558+1209C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77888500 | |||||||
chr4:77888523 | A | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0228 a0001c0001t0001g0229 others(8): Show |
12 | HG00280.hp1 HG01071.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.558+1232A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77888523 | |||||||
chr4:77888673 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.558+1382A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77888673 | |||||||
chr4:77888856 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.558+1565T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77888856 | |||||||
chr4:77888886 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.558+1595G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77888886 | |||||||
chr4:77888935 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.558+1644C>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77888935 | |||||||
chr4:77889068 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.558+1777T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77889068 | |||||||
chr4:77889072 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.558+1781C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77889072 | |||||||
chr4:77889109 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.558+1818C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77889109 | |||||||
chr4:77889196 | T | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.558+1905T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77889196 | |||||||
chr4:77889506 | C | T | 62 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(59): Show |
63 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.558+2215C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77889506 | |||||||
chr4:77889784 | A | C | 1 | a0001c0001t0001g0211 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.558+2493A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77889784 | |||||||
chr4:77889807 | G | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(75): Show |
79 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.558+2516G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77889807 | |||||||
chr4:77889889 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.558+2598A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77889889 | |||||||
chr4:77889947 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.558+2656G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77889947 | |||||||
chr4:77890003 | A | G | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.558+2712A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77890003 | |||||||
chr4:77890091 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.558+2800A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77890091 | |||||||
chr4:77890140 | A | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.558+2849A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77890140 | |||||||
chr4:77890297 | T | A | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.558+3006T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77890297 | |||||||
chr4:77890392 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.558+3101A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77890392 | |||||||
chr4:77890849 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0224 |
2 | HG01169.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.559-3290C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77890849 | |||||||
chr4:77890850 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.559-3289G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77890850 | |||||||
chr4:77890861 | A | C | 79 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(76): Show |
80 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.559-3278A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77890861 | |||||||
chr4:77890921 | G | C | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.559-3218G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77890921 | |||||||
chr4:77891113 | G | A | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.559-3026G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77891113 | |||||||
chr4:77891165 | T | A | 1 | a0001c0001t0001g0078 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.559-2974T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77891165 | |||||||
chr4:77891280 | TTTC | T | 41 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(38): Show |
44 | HG00544.hp1 HG00558.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.559-2853_559-2851d others(5): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 77891280 | ||||||
chr4:77891318 | T | C | 7 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0071 others(4): Show |
7 | HG03490.hp2 HG03492.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.559-2821T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77891318 | |||||||
chr4:77891325 | C | T | 1 | a0003c0006t0001g0201 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.559-2814C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77891325 | |||||||
chr4:77891349 | G | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.559-2790G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77891349 | |||||||
chr4:77891356 | T | G | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.559-2783T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77891356 | |||||||
chr4:77891391 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.559-2748C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77891391 | |||||||
chr4:77891501 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.559-2638G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77891501 | |||||||
chr4:77891511 | G | C | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.559-2628G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77891511 | |||||||
chr4:77891576 | G | A | 1 | a0001c0005t0001g0133 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.559-2563G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77891576 | |||||||
chr4:77891620 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.559-2519T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77891620 | |||||||
chr4:77891759 | C | G | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(200): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.559-2380C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77891759 | |||||||
chr4:77892102 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.559-2037G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77892102 | |||||||
chr4:77892127 | CT | C | 121 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.559-1999delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 77892127 | ||||||
chr4:77892141 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.559-1998C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77892141 | |||||||
chr4:77892192 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.559-1947C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77892192 | |||||||
chr4:77892200 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.559-1939C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77892200 | |||||||
chr4:77892266 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.559-1873G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77892266 | |||||||
chr4:77892385 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.559-1754C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77892385 | |||||||
chr4:77892430 | C | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.559-1709C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77892430 | |||||||
chr4:77892431 | G | A | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.559-1708G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77892431 | |||||||
chr4:77892711 | AT | A | 79 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(76): Show |
80 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.559-1426delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 77892711 | ||||||
chr4:77892728 | A | G | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.559-1411A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77892728 | |||||||
chr4:77892981 | G | GGTGA | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.559-1156_559-1155i others(6): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 77892981 | ||||||
chr4:77893174 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.559-965G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77893174 | |||||||
chr4:77893420 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.559-719G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77893420 | |||||||
chr4:77893505 | T | C | 5 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0083 others(2): Show |
5 | HG02280.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-634T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77893505 | |||||||
chr4:77893580 | CTA | C | 8 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0055 others(5): Show |
8 | HG01109.hp2 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.559-556_559-555del others(2): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 77893580 | ||||||
chr4:77893731 | T | C | 1 | a0001c0005t0001g0133 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.559-408T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77893731 | |||||||
chr4:77893893 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.559-246C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77893893 | |||||||
chr4:77893918 | A | AT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.559-210dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr4 | 77893918 | ||||||
chr4:77893937 | T | A | 1 | a0001c0001t0001g0018 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.559-202T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77893937 | |||||||
chr4:77893977 | T | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.559-162T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 5/8 | chr4 | 77893977 | |||||||
chr4:77894356 | C | G | 1 | a0001c0001t0001g0240 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.670+106C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77894356 | |||||||
chr4:77894408 | C | T | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.670+158C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77894408 | |||||||
chr4:77894685 | T | G | 1 | a0001c0001t0001g0134 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.670+435T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77894685 | |||||||
chr4:77894780 | C | G | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.670+530C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77894780 | |||||||
chr4:77895298 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.670+1048C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77895298 | |||||||
chr4:77895398 | G | GT | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0102 others(11): Show |
16 | HG00735.hp1 HG02145.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.670+1154dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77895398 | ||||||
chr4:77895433 | T | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.670+1183T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77895433 | |||||||
chr4:77895459 | A | T | 80 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(77): Show |
81 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.670+1209A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77895459 | |||||||
chr4:77895668 | G | C | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.670+1418G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77895668 | |||||||
chr4:77895773 | A | C | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0280 |
3 | HG02451.hp1 HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.670+1523A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77895773 | |||||||
chr4:77895824 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.670+1574C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77895824 | |||||||
chr4:77895970 | A | C | 17 | a0001c0001t0001g0084 a0001c0001t0002g0019 a0001c0001t0002g0020 others(14): Show |
17 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.670+1720A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77895970 | |||||||
chr4:77896149 | C | CT | 11 | a0001c0001t0001g0153 a0001c0001t0002g0082 a0002c0002t0002g0085 others(8): Show |
11 | HG00639.hp1 HG01256.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.670+1914dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77896149 | ||||||
chr4:77896210 | AC | A | 18 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0055 others(15): Show |
18 | HG00099.hp2 HG00741.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.670+1962delC | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77896210 | ||||||
chr4:77896775 | G | A | 1 | a0001c0003t0001g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.670+2525G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77896775 | |||||||
chr4:77896989 | G | A | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.670+2739G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77896989 | |||||||
chr4:77897045 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.670+2795A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77897045 | |||||||
chr4:77897068 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.670+2818A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77897068 | |||||||
chr4:77897072 | CT | C | 16 | a0001c0001t0001g0023 a0001c0001t0001g0084 a0001c0001t0002g0021 others(13): Show |
16 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.670+2832delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77897072 | ||||||
chr4:77897078 | T | C | 10 | a0001c0001t0002g0082 a0002c0002t0002g0085 a0002c0002t0002g0086 others(7): Show |
10 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.670+2828T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77897078 | |||||||
chr4:77897082 | T | A | 1 | a0001c0001t0001g0261 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.670+2832T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77897082 | |||||||
chr4:77897099 | C | G | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.670+2849C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77897099 | |||||||
chr4:77897192 | T | G | 1 | a0001c0001t0002g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.670+2942T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77897192 | |||||||
chr4:77897198 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.670+2948C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77897198 | |||||||
chr4:77897290 | G | C | 1 | a0001c0001t0001g0152 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.670+3040G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77897290 | |||||||
chr4:77897598 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.670+3348G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77897598 | |||||||
chr4:77897798 | TA | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02922.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.670+3550delA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77897798 | ||||||
chr4:77897818 | G | A | 5 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0083 others(2): Show |
5 | HG02280.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+3568G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77897818 | |||||||
chr4:77898044 | A | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.670+3794A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898044 | |||||||
chr4:77898392 | T | TTGAA | 17 | a0001c0001t0001g0084 a0001c0001t0001g0117 a0001c0001t0002g0021 others(14): Show |
17 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.670+4173_670+4176d others(6): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77898392 | ||||||
chr4:77898392 | TTGAA | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(104): Show |
115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.670+4173_670+4176d others(6): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77898392 | ||||||
chr4:77898392 | TTGAATGA others(1): Show |
T | 5 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+4169_670+4176d others(10): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77898392 | ||||||
chr4:77898392 | TTGAATGA others(5): Show |
T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+4165_670+4176d others(14): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77898392 | ||||||
chr4:77898442 | A | T | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.670+4192A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898442 | |||||||
chr4:77898553 | A | C | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.670+4303A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898553 | |||||||
chr4:77898609 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0249 |
2 | HG01169.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.670+4359G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898609 | |||||||
chr4:77898640 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.670+4390G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898640 | |||||||
chr4:77898664 | T | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.670+4414T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898664 | |||||||
chr4:77898766 | T | G | 1 | a0001c0001t0001g0126 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.670+4516T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898766 | |||||||
chr4:77898795 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.670+4545G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898795 | |||||||
chr4:77898801 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+4551T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898801 | |||||||
chr4:77898814 | G | GT | 68 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0017 others(65): Show |
70 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.670+4574dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77898814 | ||||||
chr4:77898827 | C | T | 204 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
216 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.670+4577C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898827 | |||||||
chr4:77898969 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.670+4719T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898969 | |||||||
chr4:77898988 | GAT | G | 8 | a0001c0001t0001g0024 a0001c0001t0001g0031 a0001c0001t0001g0033 others(5): Show |
8 | HG01109.hp2 HG02129.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+4739_670+4740d others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898988 | |||||||
chr4:77898988 | GATT | G | 54 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(51): Show |
55 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.670+4739_670+4741d others(5): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77898988 | |||||||
chr4:77898989 | A | AT | 25 | a0001c0001t0001g0006 a0001c0001t0001g0111 a0001c0001t0001g0115 others(22): Show |
25 | HG00438.hp1 HG00639.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.670+4761dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77898989 | ||||||
chr4:77898989 | AT | A | 28 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(25): Show |
31 | HG00544.hp1 HG01255.hp2 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.670+4761delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77898989 | ||||||
chr4:77899150 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.670+4900C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77899150 | |||||||
chr4:77899153 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.670+4903C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77899153 | |||||||
chr4:77899160 | A | AT | 18 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(15): Show |
21 | HG00323.hp2 HG01192.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.670+4928dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77899160 | ||||||
chr4:77899160 | ATT | A | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.670+4927_670+4928d others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77899160 | ||||||
chr4:77899224 | C | G | 2 | a0001c0001t0001g0046 a0001c0001t0001g0067 |
2 | NA19001.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.670+4974C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77899224 | |||||||
chr4:77899310 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02129.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.670+5060T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77899310 | |||||||
chr4:77899359 | G | T | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
120 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.670+5109G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77899359 | |||||||
chr4:77899595 | C | G | 1 | a0001c0001t0001g0143 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.670+5345C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77899595 | |||||||
chr4:77899619 | A | G | 62 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(59): Show |
63 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.670+5369A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77899619 | |||||||
chr4:77899622 | C | G | 5 | a0001c0001t0001g0228 a0001c0001t0001g0230 a0001c0001t0001g0241 others(2): Show |
5 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+5372C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77899622 | |||||||
chr4:77899837 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.670+5587A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77899837 | |||||||
chr4:77900028 | A | C | 1 | a0001c0001t0001g0027 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.670+5778A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77900028 | |||||||
chr4:77900182 | A | C | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.670+5932A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77900182 | |||||||
chr4:77900201 | G | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.670+5951G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77900201 | |||||||
chr4:77900229 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+5979T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77900229 | |||||||
chr4:77900355 | G | T | 5 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
5 | HG02258.hp2 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+6105G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77900355 | |||||||
chr4:77900401 | G | C | 2 | a0001c0001t0001g0265 a0001c0001t0001g0267 |
2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.670+6151G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77900401 | |||||||
chr4:77900440 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.670+6190G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77900440 | |||||||
chr4:77900499 | C | G | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.670+6249C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77900499 | |||||||
chr4:77900521 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.670+6271C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77900521 | |||||||
chr4:77901169 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.670+6919T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77901169 | |||||||
chr4:77901185 | C | T | 10 | a0001c0001t0001g0026 a0001c0001t0001g0122 a0001c0001t0001g0153 others(7): Show |
10 | HG00423.hp2 HG00642.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.670+6935C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77901185 | |||||||
chr4:77901469 | TA | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(5): Show |
8 | HG02129.hp2 NA18747.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+7231delA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77901469 | ||||||
chr4:77901656 | G | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0102 others(11): Show |
16 | HG00735.hp1 HG02145.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.670+7406G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77901656 | |||||||
chr4:77901916 | C | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(61): Show |
65 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.671-7350C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77901916 | |||||||
chr4:77902007 | G | A | 1 | a0003c0006t0001g0201 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.671-7259G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77902007 | |||||||
chr4:77902032 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.671-7234A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77902032 | |||||||
chr4:77902159 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.671-7107T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77902159 | |||||||
chr4:77902322 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.671-6944T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77902322 | |||||||
chr4:77902346 | C | G | 1 | a0002c0002t0002g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.671-6920C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77902346 | |||||||
chr4:77902352 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.671-6914T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77902352 | |||||||
chr4:77902385 | T | TA | 69 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(66): Show |
71 | HG00438.hp1 HG00639.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.671-6861dupA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77902385 | ||||||
chr4:77902385 | T | TAA | 10 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0057 others(7): Show |
10 | HG00099.hp2 HG00741.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.671-6862_671-6861d others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77902385 | ||||||
chr4:77902385 | TA | T | 14 | a0001c0001t0001g0084 a0001c0001t0001g0134 a0001c0001t0002g0021 others(11): Show |
14 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.671-6861delA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77902385 | ||||||
chr4:77902637 | T | A | 9 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(6): Show |
9 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.671-6629T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77902637 | |||||||
chr4:77902638 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.671-6628A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77902638 | |||||||
chr4:77902679 | T | A | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.671-6587T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77902679 | |||||||
chr4:77902754 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.671-6512A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77902754 | |||||||
chr4:77902861 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.671-6405G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77902861 | |||||||
chr4:77902879 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.671-6387A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77902879 | |||||||
chr4:77903028 | A | C | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.671-6238A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77903028 | |||||||
chr4:77903149 | T | TAAAAATA others(28): Show |
1 | a0001c0001t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.671-6114_671-6113i others(37): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77903149 | ||||||
chr4:77903153 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.671-6113G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77903153 | |||||||
chr4:77903154 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.671-6112G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77903154 | |||||||
chr4:77903220 | A | G | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.671-6046A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77903220 | |||||||
chr4:77903263 | TATC | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(61): Show |
65 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.671-5999_671-5997d others(5): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77903263 | ||||||
chr4:77903294 | C | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.671-5972C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77903294 | |||||||
chr4:77903520 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.671-5746A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77903520 | |||||||
chr4:77903884 | A | T | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.671-5382A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77903884 | |||||||
chr4:77903998 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.671-5268T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77903998 | |||||||
chr4:77904022 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.671-5244G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77904022 | |||||||
chr4:77904084 | TA | T | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
212 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.671-5169delA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77904084 | ||||||
chr4:77904106 | G | A | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.671-5160G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77904106 | |||||||
chr4:77904276 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0123 a0001c0001t0001g0250 |
5 | HG01243.hp2 HG01891.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.671-4990G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77904276 | |||||||
chr4:77904595 | A | C | 1 | a0001c0001t0001g0227 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.671-4671A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77904595 | |||||||
chr4:77904632 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.671-4634A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77904632 | |||||||
chr4:77904643 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.671-4623G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77904643 | |||||||
chr4:77904867 | A | G | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.671-4399A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77904867 | |||||||
chr4:77905222 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.671-4044C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77905222 | |||||||
chr4:77905491 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.671-3775C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77905491 | |||||||
chr4:77905496 | C | CA | 50 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
59 | HG00280.hp1 HG00544.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.671-3746dupA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77905496 | ||||||
chr4:77905496 | C | CAA | 70 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0023 others(67): Show |
72 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.671-3747_671-3746d others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77905496 | ||||||
chr4:77905496 | C | CAAA | 10 | a0001c0001t0001g0099 a0001c0001t0001g0122 a0001c0001t0001g0134 others(7): Show |
10 | HG00438.hp2 HG01433.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.671-3748_671-3746d others(5): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77905496 | ||||||
chr4:77905496 | CA | C | 56 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0022 others(53): Show |
56 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.671-3746delA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77905496 | ||||||
chr4:77905527 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0192 |
2 | HG00323.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.671-3739A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77905527 | |||||||
chr4:77905617 | G | A | 10 | a0001c0001t0002g0082 a0002c0002t0002g0085 a0002c0002t0002g0086 others(7): Show |
10 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.671-3649G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77905617 | |||||||
chr4:77905747 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.671-3519T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77905747 | |||||||
chr4:77905881 | G | T | 80 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(77): Show |
81 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.671-3385G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77905881 | |||||||
chr4:77906019 | T | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
121 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.671-3247T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77906019 | |||||||
chr4:77906134 | C | A | 1 | a0001c0001t0002g0082 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.671-3132C>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77906134 | |||||||
chr4:77906519 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0262 |
2 | HG00323.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.671-2747A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77906519 | |||||||
chr4:77906841 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.671-2425A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77906841 | |||||||
chr4:77906848 | C | G | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.671-2418C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77906848 | |||||||
chr4:77907060 | C | G | 1 | a0001c0001t0001g0195 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.671-2206C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77907060 | |||||||
chr4:77907106 | C | G | 1 | a0001c0001t0001g0027 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.671-2160C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77907106 | |||||||
chr4:77907500 | GTC | G | 121 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.671-1755_671-1754d others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77907500 | ||||||
chr4:77907527 | C | CCT | 9 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(6): Show |
9 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.671-1723_671-1722d others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77907527 | ||||||
chr4:77907713 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.671-1553C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77907713 | |||||||
chr4:77907760 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.671-1506C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77907760 | |||||||
chr4:77907763 | C | T | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.671-1503C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77907763 | |||||||
chr4:77907892 | C | CT | 23 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0033 others(20): Show |
26 | HG00438.hp1 HG00639.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.671-1359dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77907892 | ||||||
chr4:77908230 | C | T | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.671-1036C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77908230 | |||||||
chr4:77908245 | T | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0106 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.671-1021T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77908245 | |||||||
chr4:77908795 | G | A | 60 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(57): Show |
61 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.671-471G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77908795 | |||||||
chr4:77908799 | G | T | 15 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0082 others(12): Show |
15 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.671-467G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | chr4 | 77908799 | |||||||
chr4:77909118 | AAC | A | 95 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.671-145_671-144del others(2): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr4 | 77909118 | ||||||
chr4:77909430 | C | T | 80 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(77): Show |
81 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.777+58C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77909430 | |||||||
chr4:77909547 | A | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0080 |
3 | HG02145.hp2 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.777+175A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77909547 | |||||||
chr4:77909652 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.777+280G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77909652 | |||||||
chr4:77909744 | A | C | 1 | a0001c0001t0001g0059 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.777+372A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77909744 | |||||||
chr4:77909745 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.777+373A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77909745 | |||||||
chr4:77909988 | T | C | 61 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(58): Show |
62 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.777+616T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77909988 | |||||||
chr4:77910147 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.777+775C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77910147 | |||||||
chr4:77910167 | A | C | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+795A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77910167 | |||||||
chr4:77910546 | T | C | 1 | a0002c0002t0002g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.777+1174T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77910546 | |||||||
chr4:77911088 | G | C | 1 | a0001c0001t0002g0082 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.777+1716G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77911088 | |||||||
chr4:77911300 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.777+1928A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77911300 | |||||||
chr4:77911392 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.777+2020C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77911392 | |||||||
chr4:77911423 | A | ACTACTTG others(8): Show |
80 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(77): Show |
81 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.777+2051_777+2052i others(17): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77911423 | |||||||
chr4:77911505 | A | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+2133A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77911505 | |||||||
chr4:77911594 | C | A | 1 | a0001c0003t0001g0066 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.777+2222C>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77911594 | |||||||
chr4:77911670 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.777+2298T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77911670 | |||||||
chr4:77911722 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+2350G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77911722 | |||||||
chr4:77911778 | C | G | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+2406C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77911778 | |||||||
chr4:77911804 | T | C | 1 | a0001c0001t0002g0082 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.777+2432T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77911804 | |||||||
chr4:77911891 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.777+2519T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77911891 | |||||||
chr4:77912183 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG01109.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.777+2811C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77912183 | |||||||
chr4:77912233 | G | C | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+2861G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77912233 | |||||||
chr4:77912370 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0001g0053 |
2 | HG02132.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.777+2998A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77912370 | |||||||
chr4:77912622 | C | G | 2 | a0001c0001t0001g0265 a0001c0001t0001g0267 |
2 | HG00280.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.777+3250C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77912622 | |||||||
chr4:77913175 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.777+3803C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77913175 | |||||||
chr4:77913376 | G | A | 5 | a0001c0001t0001g0084 a0001c0001t0002g0021 a0001c0001t0002g0083 others(2): Show |
5 | HG02280.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.777+4004G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77913376 | |||||||
chr4:77913378 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.777+4006T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77913378 | |||||||
chr4:77913537 | C | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0127 |
2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.777+4165C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77913537 | |||||||
chr4:77913546 | G | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0075 a0001c0001t0001g0080 |
3 | HG02145.hp2 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.777+4174G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77913546 | |||||||
chr4:77913680 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.777+4308C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77913680 | |||||||
chr4:77913709 | C | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.777+4337C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77913709 | |||||||
chr4:77913730 | A | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0282 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.777+4358A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77913730 | |||||||
chr4:77913791 | A | G | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0163 others(1): Show |
4 | HG00423.hp2 NA18940.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+4419A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77913791 | |||||||
chr4:77913857 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.777+4485A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77913857 | |||||||
chr4:77914032 | T | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(3): Show |
6 | HG02129.hp2 NA18747.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+4660T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77914032 | |||||||
chr4:77914180 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.777+4808C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77914180 | |||||||
chr4:77914345 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.777+4973G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77914345 | |||||||
chr4:77914401 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02129.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.777+5029G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77914401 | |||||||
chr4:77914457 | C | G | 1 | a0001c0001t0001g0229 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.777+5085C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77914457 | |||||||
chr4:77914496 | A | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0102 others(13): Show |
18 | HG00735.hp1 HG01243.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.777+5124A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77914496 | |||||||
chr4:77914549 | A | G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.777+5177A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77914549 | |||||||
chr4:77914610 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG01109.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.777+5238A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77914610 | |||||||
chr4:77914664 | G | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0050 |
2 | NA18957.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.777+5292G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77914664 | |||||||
chr4:77914685 | T | C | 1 | a0002c0002t0002g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.777+5313T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77914685 | |||||||
chr4:77914687 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.777+5315G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77914687 | |||||||
chr4:77914709 | T | TTG | 6 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0210 others(3): Show |
8 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.777+5357_777+5358d others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77914709 | ||||||
chr4:77914727 | G | GTGTT | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.777+5358_777+5359i others(6): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77914727 | ||||||
chr4:77914727 | G | GTT | 24 | a0001c0001t0001g0023 a0001c0001t0001g0117 a0001c0001t0001g0118 others(21): Show |
24 | HG00639.hp1 HG01243.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.777+5356_777+5357i others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77914727 | ||||||
chr4:77915032 | A | G | 61 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(58): Show |
62 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.777+5660A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77915032 | |||||||
chr4:77915201 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.777+5829A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77915201 | |||||||
chr4:77915291 | G | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+5919G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77915291 | |||||||
chr4:77915474 | A | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.777+6102A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77915474 | |||||||
chr4:77915596 | G | T | 1 | a0001c0001t0001g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.777+6224G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77915596 | |||||||
chr4:77915614 | A | G | 35 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0022 others(32): Show |
35 | HG00673.hp2 HG01928.hp1 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.777+6242A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77915614 | |||||||
chr4:77915738 | C | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.777+6366C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77915738 | |||||||
chr4:77915881 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.777+6509T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77915881 | |||||||
chr4:77915986 | A | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.777+6614A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77915986 | |||||||
chr4:77916327 | T | TAAGAAAC others(274): Show |
1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+6968_777+6969i others(283): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77916327 | ||||||
chr4:77916428 | A | G | 17 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(14): Show |
17 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.777+7056A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77916428 | |||||||
chr4:77916720 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.777+7348G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77916720 | |||||||
chr4:77916756 | T | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.777+7384T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77916756 | |||||||
chr4:77916971 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.777+7599G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77916971 | |||||||
chr4:77917058 | T | C | 1 | a0001c0001t0002g0082 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.777+7686T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77917058 | |||||||
chr4:77917103 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.777+7731C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77917103 | |||||||
chr4:77917186 | T | A | 1 | a0002c0002t0002g0087 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.777+7814T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77917186 | |||||||
chr4:77917474 | G | C | 1 | a0002c0002t0002g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.777+8102G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77917474 | |||||||
chr4:77917566 | T | TA | 6 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0125 others(3): Show |
6 | HG02723.hp2 HG03486.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.777+8203dupA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77917566 | ||||||
chr4:77917596 | A | G | 83 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(80): Show |
84 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.777+8224A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77917596 | |||||||
chr4:77917708 | C | G | 83 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(80): Show |
84 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.777+8336C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77917708 | |||||||
chr4:77917769 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.777+8397T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77917769 | |||||||
chr4:77917815 | G | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0229 a0001c0001t0001g0230 others(6): Show |
10 | HG00280.hp1 HG01071.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.777+8443G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77917815 | |||||||
chr4:77917843 | G | A | 82 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.777+8471G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77917843 | |||||||
chr4:77917864 | C | T | 82 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.777+8492C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77917864 | |||||||
chr4:77917905 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.777+8533A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77917905 | |||||||
chr4:77917927 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.777+8555A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77917927 | |||||||
chr4:77918049 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0050 |
2 | NA18957.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.777+8677A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77918049 | |||||||
chr4:77918053 | C | CA | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0022 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.777+8697dupA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77918053 | ||||||
chr4:77918210 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0108 a0001c0001t0001g0112 |
4 | HG00735.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+8838C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77918210 | |||||||
chr4:77918463 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.777+9091T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77918463 | |||||||
chr4:77918967 | A | C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(80): Show |
84 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.777+9595A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77918967 | |||||||
chr4:77919174 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+9802G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77919174 | |||||||
chr4:77919293 | C | T | 95 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.777+9921C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77919293 | |||||||
chr4:77919338 | A | G | 11 | a0001c0001t0002g0082 a0001c0001t0002g0280 a0002c0002t0002g0085 others(8): Show |
11 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.777+9966A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77919338 | |||||||
chr4:77919477 | TTCA | T | 17 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(14): Show |
17 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.777+10106_777+1010 others(7): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77919477 | |||||||
chr4:77919624 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.777+10252C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77919624 | |||||||
chr4:77919679 | T | G | 1 | a0001c0001t0001g0134 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.777+10307T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77919679 | |||||||
chr4:77919716 | T | A | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.777+10344T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77919716 | |||||||
chr4:77919797 | AATAT | A | 82 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.777+10432_777+1043 others(8): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77919797 | ||||||
chr4:77919835 | T | TTA | 13 | a0001c0001t0002g0021 a0001c0001t0002g0082 a0001c0001t0002g0083 others(10): Show |
13 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.777+10477_777+1047 others(6): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77919835 | ||||||
chr4:77919849 | A | ATATG | 59 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(56): Show |
60 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.777+10478_777+1047 others(8): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77919849 | ||||||
chr4:77919849 | A | ATG | 15 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0106 others(12): Show |
17 | HG00735.hp1 HG01358.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.777+10495_777+1049 others(6): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77919849 | ||||||
chr4:77919849 | A | ATGTG | 3 | a0001c0001t0002g0094 a0001c0001t0002g0095 a0001c0001t0002g0234 |
3 | HG02280.hp1 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.777+10493_777+1049 others(8): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77919849 | ||||||
chr4:77919849 | A | G | 12 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0023 others(9): Show |
15 | HG00423.hp2 HG01243.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.777+10477A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77919849 | |||||||
chr4:77919935 | G | A | 17 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(14): Show |
17 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.777+10563G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77919935 | |||||||
chr4:77920155 | G | T | 9 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(6): Show |
9 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.777+10783G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77920155 | |||||||
chr4:77920234 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.777+10862T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77920234 | |||||||
chr4:77920295 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.777+10923T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77920295 | |||||||
chr4:77920320 | T | A | 6 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0083 others(3): Show |
6 | HG02280.hp1 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+10948T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77920320 | |||||||
chr4:77920450 | A | C | 1 | a0001c0003t0001g0065 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.777+11078A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77920450 | |||||||
chr4:77920718 | G | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(80): Show |
84 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.777+11346G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77920718 | |||||||
chr4:77920766 | CT | C | 17 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(14): Show |
17 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.777+11403delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77920766 | ||||||
chr4:77920951 | G | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.777+11579G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77920951 | |||||||
chr4:77921011 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.777+11639C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77921011 | |||||||
chr4:77921012 | G | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.777+11640G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77921012 | |||||||
chr4:77921127 | G | A | 83 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(80): Show |
84 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.777+11755G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77921127 | |||||||
chr4:77921252 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG02129.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.777+11880A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77921252 | |||||||
chr4:77921422 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.777+12050T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77921422 | |||||||
chr4:77921523 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.777+12151A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77921523 | |||||||
chr4:77921551 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.777+12179G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77921551 | |||||||
chr4:77921623 | C | T | 9 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(6): Show |
9 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.777+12251C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77921623 | |||||||
chr4:77921772 | GT | G | 72 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(69): Show |
73 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.777+12415delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77921772 | ||||||
chr4:77921976 | C | T | 11 | a0001c0001t0002g0082 a0001c0001t0002g0280 a0002c0002t0002g0085 others(8): Show |
11 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.777+12604C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77921976 | |||||||
chr4:77922223 | A | G | 1 | a0001c0001t0001g0018 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.777+12851A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77922223 | |||||||
chr4:77922246 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.777+12874G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77922246 | |||||||
chr4:77922358 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
131 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.777+12986G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77922358 | |||||||
chr4:77922471 | G | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.777+13099G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77922471 | |||||||
chr4:77922666 | T | C | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.777+13294T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77922666 | |||||||
chr4:77922739 | A | G | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(203): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.777+13367A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77922739 | |||||||
chr4:77922761 | T | C | 206 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(203): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.777+13389T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77922761 | |||||||
chr4:77923520 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.777+14148T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77923520 | |||||||
chr4:77923527 | C | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0259 |
2 | NA18953.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.777+14155C>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77923527 | |||||||
chr4:77923581 | C | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0059 |
3 | HG01928.hp1 HG02004.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.777+14209C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77923581 | |||||||
chr4:77923627 | G | T | 3 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0073 |
3 | HG02818.hp2 HG03225.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.777+14255G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77923627 | |||||||
chr4:77923797 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.777+14425C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77923797 | |||||||
chr4:77924000 | CA | C | 195 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.777+14642delA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77924000 | ||||||
chr4:77924000 | CAA | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0123 others(5): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.777+14641_777+1464 others(6): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77924000 | ||||||
chr4:77924012 | A | G | 1 | a0001c0001t0001g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.777+14640A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77924012 | |||||||
chr4:77924041 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.777+14669A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77924041 | |||||||
chr4:77924231 | A | AGTGGTGT | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(200): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.777+14862_777+1486 others(11): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77924231 | ||||||
chr4:77924528 | A | C | 1 | a0001c0001t0001g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.777+15156A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77924528 | |||||||
chr4:77924561 | T | A | 1 | a0002c0002t0002g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.777+15189T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77924561 | |||||||
chr4:77924602 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+15230A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77924602 | |||||||
chr4:77924984 | T | C | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.777+15612T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77924984 | |||||||
chr4:77925047 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.777+15675C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77925047 | |||||||
chr4:77925190 | C | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.777+15818C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77925190 | |||||||
chr4:77925208 | A | G | 8 | a0001c0001t0001g0039 a0001c0001t0001g0047 a0001c0001t0001g0055 others(5): Show |
8 | HG01109.hp2 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.777+15836A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77925208 | |||||||
chr4:77925341 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.777+15969T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77925341 | |||||||
chr4:77925342 | T | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.777+15970T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77925342 | |||||||
chr4:77925383 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.777+16011G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77925383 | |||||||
chr4:77925502 | C | T | 9 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(6): Show |
9 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.777+16130C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77925502 | |||||||
chr4:77925607 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+16235G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77925607 | |||||||
chr4:77925826 | C | T | 11 | a0001c0001t0001g0105 a0001c0001t0001g0125 a0001c0001t0001g0132 others(8): Show |
11 | HG00741.hp1 HG01099.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.777+16454C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77925826 | |||||||
chr4:77925893 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.777+16521A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77925893 | |||||||
chr4:77926576 | A | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.777+17204A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77926576 | |||||||
chr4:77926581 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+17209A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77926581 | |||||||
chr4:77926612 | C | CT | 120 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
131 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.777+17254dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77926612 | ||||||
chr4:77926626 | T | C | 4 | a0001c0001t0002g0082 a0001c0001t0002g0094 a0001c0001t0002g0095 others(1): Show |
4 | HG02280.hp1 HG02735.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+17254T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77926626 | |||||||
chr4:77926626 | T | TC | 76 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(73): Show |
77 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.777+17254_777+1725 others(5): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77926626 | |||||||
chr4:77926685 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG00280.hp1 HG01071.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.777+17313C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77926685 | |||||||
chr4:77926764 | G | A | 8 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(5): Show |
8 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.777+17392G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77926764 | |||||||
chr4:77926851 | C | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.777+17479C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77926851 | |||||||
chr4:77926884 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.777+17512C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77926884 | |||||||
chr4:77926901 | A | G | 1 | a0002c0002t0002g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.777+17529A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77926901 | |||||||
chr4:77927031 | C | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.777+17659C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77927031 | |||||||
chr4:77927071 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0152 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.777+17699T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77927071 | |||||||
chr4:77927247 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+17875A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77927247 | |||||||
chr4:77927721 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.777+18349A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77927721 | |||||||
chr4:77927768 | A | T | 120 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
131 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.777+18396A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77927768 | |||||||
chr4:77927898 | C | T | 35 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0022 others(32): Show |
35 | HG00673.hp2 HG01928.hp1 HG02004.hp1 others(32): Show |
intron_variant | MODIFIER | c.777+18526C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77927898 | |||||||
chr4:77927934 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
131 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.777+18562G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77927934 | |||||||
chr4:77927957 | G | C | 1 | a0001c0001t0001g0018 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.777+18585G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77927957 | |||||||
chr4:77927969 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.777+18597A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77927969 | |||||||
chr4:77928030 | T | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0282 |
3 | HG02572.hp1 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.777+18658T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77928030 | |||||||
chr4:77928573 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.777+19201C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77928573 | |||||||
chr4:77929048 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+19676G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929048 | |||||||
chr4:77929066 | C | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.777+19694C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929066 | |||||||
chr4:77929073 | C | G | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(202): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.777+19701C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929073 | |||||||
chr4:77929212 | C | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.777+19840C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929212 | |||||||
chr4:77929253 | C | T | 2 | a0001c0001t0002g0121 a0001c0001t0002g0127 |
2 | HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.777+19881C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929253 | |||||||
chr4:77929277 | TA | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(78): Show |
82 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.777+19910delA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77929277 | ||||||
chr4:77929303 | G | C | 16 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(13): Show |
16 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.777+19931G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929303 | |||||||
chr4:77929426 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.777+20054A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929426 | |||||||
chr4:77929462 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.777+20090A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929462 | |||||||
chr4:77929471 | G | A | 82 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.777+20099G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929471 | |||||||
chr4:77929730 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.778-20067A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929730 | |||||||
chr4:77929769 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.778-20028T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929769 | |||||||
chr4:77929769 | T | TA | 19 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0044 others(16): Show |
21 | HG00735.hp1 HG01243.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-20017dupA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77929769 | ||||||
chr4:77929769 | T | TAA | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(178): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.778-20018_778-2001 others(6): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77929769 | ||||||
chr4:77929826 | T | C | 2 | a0001c0001t0002g0062 a0001c0001t0002g0083 |
2 | HG02559.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.778-19971T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929826 | |||||||
chr4:77929904 | A | G | 6 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0083 others(3): Show |
6 | HG02280.hp1 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-19893A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77929904 | |||||||
chr4:77930321 | A | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.778-19476A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77930321 | |||||||
chr4:77930683 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.778-19114G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77930683 | |||||||
chr4:77930786 | T | G | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(200): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.778-19011T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77930786 | |||||||
chr4:77930831 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.778-18966C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77930831 | |||||||
chr4:77930995 | A | C | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-18802A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77930995 | |||||||
chr4:77931037 | C | T | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.778-18760C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77931037 | |||||||
chr4:77931340 | G | C | 1 | a0001c0003t0001g0068 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.778-18457G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77931340 | |||||||
chr4:77931437 | C | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(80): Show |
84 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.778-18360C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77931437 | |||||||
chr4:77931512 | T | C | 17 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(14): Show |
17 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.778-18285T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77931512 | |||||||
chr4:77931528 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(204): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.778-18269C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77931528 | |||||||
chr4:77931538 | G | T | 2 | a0001c0001t0001g0205 a0001c0001t0001g0220 |
2 | NA18939.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.778-18259G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77931538 | |||||||
chr4:77931559 | T | C | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(200): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.778-18238T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77931559 | |||||||
chr4:77931620 | T | A | 83 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(80): Show |
84 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.778-18177T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77931620 | |||||||
chr4:77931863 | T | TTAAAATT others(4020): Show |
1 | a0001c0005t0001g0133 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.778-17917_778-1791 others(4031): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77931863 | ||||||
chr4:77931863 | T | TTAAAATT others(4033): Show |
1 | a0001c0001t0001g0140 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.778-17917_778-1791 others(4044): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77931863 | ||||||
chr4:77931863 | T | TTAAAATT others(4030): Show |
1 | a0001c0001t0001g0141 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.778-17917_778-1791 others(4041): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77931863 | ||||||
chr4:77931905 | A | G | 83 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(80): Show |
84 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.778-17892A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77931905 | |||||||
chr4:77932090 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.778-17707A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77932090 | |||||||
chr4:77932398 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0167 |
2 | NA18964.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.778-17399C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77932398 | |||||||
chr4:77932449 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.778-17348A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77932449 | |||||||
chr4:77932463 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-17334C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77932463 | |||||||
chr4:77932563 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.778-17234G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77932563 | |||||||
chr4:77932618 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.778-17179G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77932618 | |||||||
chr4:77932693 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0152 |
2 | HG01192.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.778-17104C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77932693 | |||||||
chr4:77932708 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.778-17089C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77932708 | |||||||
chr4:77932714 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0079 |
3 | NA18978.hp1 NA18982.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.778-17083G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77932714 | |||||||
chr4:77932863 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.778-16934T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77932863 | |||||||
chr4:77932973 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-16824G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77932973 | |||||||
chr4:77933104 | G | A | 11 | a0001c0001t0002g0082 a0001c0001t0002g0280 a0002c0002t0002g0085 others(8): Show |
11 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.778-16693G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77933104 | |||||||
chr4:77933138 | G | C | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-16659G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77933138 | |||||||
chr4:77933162 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.778-16635C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77933162 | |||||||
chr4:77933203 | C | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.778-16594C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77933203 | |||||||
chr4:77933239 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.778-16558C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77933239 | |||||||
chr4:77933502 | A | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02922.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.778-16295A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77933502 | |||||||
chr4:77933695 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.778-16102C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77933695 | |||||||
chr4:77933788 | C | T | 17 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(14): Show |
17 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.778-16009C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77933788 | |||||||
chr4:77934610 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
131 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.778-15187G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77934610 | |||||||
chr4:77934765 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.778-15032A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77934765 | |||||||
chr4:77935168 | G | C | 6 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0083 others(3): Show |
6 | HG02280.hp1 HG02559.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-14629G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77935168 | |||||||
chr4:77935931 | C | CA | 120 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
131 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.778-13850dupA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77935931 | ||||||
chr4:77935946 | A | AAT | 18 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(15): Show |
18 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.778-13850_778-1384 others(6): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77935946 | ||||||
chr4:77935946 | A | AT | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.778-13851_778-1385 others(5): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77935946 | |||||||
chr4:77936050 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.778-13747A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77936050 | |||||||
chr4:77936107 | G | A | 83 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(80): Show |
84 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.778-13690G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77936107 | |||||||
chr4:77936168 | A | AT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(120): Show |
129 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.778-13619dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77936168 | ||||||
chr4:77936380 | A | C | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-13417A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77936380 | |||||||
chr4:77936808 | G | A | 2 | a0001c0001t0001g0160 a0001c0001t0001g0168 |
2 | NA18947.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.778-12989G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77936808 | |||||||
chr4:77936993 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.778-12804C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77936993 | |||||||
chr4:77937021 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.778-12776A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77937021 | |||||||
chr4:77937109 | A | T | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.778-12688A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77937109 | |||||||
chr4:77937156 | G | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.778-12641G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77937156 | |||||||
chr4:77937334 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.778-12463T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77937334 | |||||||
chr4:77937361 | A | G | 203 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(200): Show |
215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.778-12436A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77937361 | |||||||
chr4:77937425 | C | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.778-12372C>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77937425 | |||||||
chr4:77937510 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02922.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.778-12287G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77937510 | |||||||
chr4:77937964 | A | G | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.778-11833A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77937964 | |||||||
chr4:77937992 | A | G | 9 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(6): Show |
9 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-11805A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77937992 | |||||||
chr4:77938102 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.778-11695G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77938102 | |||||||
chr4:77938131 | G | A | 9 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(6): Show |
9 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-11666G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77938131 | |||||||
chr4:77938252 | G | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(60): Show |
64 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.778-11545G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77938252 | |||||||
chr4:77938351 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.778-11446A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77938351 | |||||||
chr4:77938409 | C | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0016 others(89): Show |
96 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.778-11388C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77938409 | |||||||
chr4:77938442 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0020 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.778-11355C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77938442 | |||||||
chr4:77938462 | A | G | 9 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(6): Show |
9 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-11335A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77938462 | |||||||
chr4:77938483 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.778-11314T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77938483 | |||||||
chr4:77938715 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.778-11082T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77938715 | |||||||
chr4:77938723 | A | G | 2 | a0001c0001t0001g0233 a0001c0001t0001g0235 |
2 | HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.778-11074A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77938723 | |||||||
chr4:77938833 | T | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0119 |
2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.778-10964T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77938833 | |||||||
chr4:77938920 | A | C | 1 | a0001c0001t0001g0255 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.778-10877A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77938920 | |||||||
chr4:77939035 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.778-10762T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77939035 | |||||||
chr4:77939211 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.778-10586C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77939211 | |||||||
chr4:77939382 | A | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0246 |
2 | HG00280.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.778-10415A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77939382 | |||||||
chr4:77939403 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.778-10394C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77939403 | |||||||
chr4:77939477 | C | T | 9 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(6): Show |
9 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.778-10320C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77939477 | |||||||
chr4:77939915 | T | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0279 |
2 | HG01978.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.778-9882T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77939915 | |||||||
chr4:77940020 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.778-9777A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77940020 | |||||||
chr4:77940087 | C | T | 21 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
21 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-9710C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77940087 | |||||||
chr4:77940672 | G | A | 64 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(61): Show |
65 | HG00099.hp2 HG00673.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.778-9125G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77940672 | |||||||
chr4:77941031 | T | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0018 others(83): Show |
87 | HG00099.hp2 HG00639.hp1 HG00673.hp2 others(84): Show |
intron_variant | MODIFIER | c.778-8766T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77941031 | |||||||
chr4:77941122 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.778-8675G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77941122 | |||||||
chr4:77941128 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.778-8669G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77941128 | |||||||
chr4:77941211 | T | C | 7 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(4): Show |
7 | HG02280.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-8586T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77941211 | |||||||
chr4:77941267 | GA | G | 21 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
21 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-8516delA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77941267 | ||||||
chr4:77941297 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.778-8500T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77941297 | |||||||
chr4:77941304 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0061 a0001c0001t0001g0067 |
3 | HG00673.hp2 NA19001.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.778-8493G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77941304 | |||||||
chr4:77942164 | C | G | 21 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
21 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-7633C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77942164 | |||||||
chr4:77942280 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.778-7517A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77942280 | |||||||
chr4:77942343 | G | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | NA18747.hp1 NA18967.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.778-7454G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77942343 | |||||||
chr4:77942412 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.778-7385T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77942412 | |||||||
chr4:77942771 | G | A | 93 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(90): Show |
99 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.778-7026G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77942771 | |||||||
chr4:77942984 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.778-6813A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77942984 | |||||||
chr4:77943159 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.778-6638A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77943159 | |||||||
chr4:77943237 | G | C | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.778-6560G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77943237 | |||||||
chr4:77943455 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0282 |
2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.778-6342C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77943455 | |||||||
chr4:77943723 | T | G | 21 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
21 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-6074T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77943723 | |||||||
chr4:77943749 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.778-6048G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77943749 | |||||||
chr4:77944515 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.778-5282A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77944515 | |||||||
chr4:77944791 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.778-5006C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77944791 | |||||||
chr4:77944853 | G | A | 95 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.778-4944G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77944853 | |||||||
chr4:77945128 | A | AATT | 93 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(90): Show |
99 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.778-4628_778-4626d others(5): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77945128 | ||||||
chr4:77945128 | A | AATTATT | 14 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0053 others(11): Show |
14 | HG00099.hp2 HG00544.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.778-4631_778-4626d others(8): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77945128 | ||||||
chr4:77945128 | A | AATTATTA others(2): Show |
3 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0269 |
3 | HG03471.hp2 HG04184.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.778-4634_778-4626d others(11): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77945128 | ||||||
chr4:77945128 | AATT | A | 34 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0035 others(31): Show |
36 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.778-4628_778-4626d others(5): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77945128 | ||||||
chr4:77945128 | AATTATT | A | 92 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
99 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.778-4631_778-4626d others(8): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77945128 | ||||||
chr4:77945169 | TTAC | T | 21 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
21 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-4614_778-4612d others(5): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77945169 | ||||||
chr4:77945209 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0210 others(1): Show |
6 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-4588G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77945209 | |||||||
chr4:77945505 | CT | C | 34 | a0001c0001t0001g0144 a0001c0001t0001g0193 a0001c0001t0001g0227 others(31): Show |
34 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.778-4281delT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77945505 | ||||||
chr4:77945574 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.778-4223G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77945574 | |||||||
chr4:77945649 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(71): Show |
81 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.778-4148A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77945649 | |||||||
chr4:77945716 | G | A | 21 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
21 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-4081G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77945716 | |||||||
chr4:77945788 | G | T | 3 | a0001c0001t0001g0222 a0001c0001t0001g0265 a0001c0001t0001g0267 |
3 | HG00280.hp2 HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.778-4009G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77945788 | |||||||
chr4:77946005 | A | G | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(217): Show |
238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.778-3792A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77946005 | |||||||
chr4:77946144 | C | T | 1 | a0001c0001t0001g0004 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.778-3653C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77946144 | |||||||
chr4:77946292 | C | T | 21 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
21 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-3505C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77946292 | |||||||
chr4:77946352 | T | TGATGTCA others(332): Show |
1 | a0001c0001t0002g0280 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.778-3430_778-3429i others(341): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77946352 | ||||||
chr4:77946489 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-3308G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77946489 | |||||||
chr4:77946834 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-2963C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77946834 | |||||||
chr4:77946942 | A | T | 1 | a0001c0001t0001g0018 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.778-2855A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77946942 | |||||||
chr4:77947011 | CA | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.778-2771delA | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77947011 | ||||||
chr4:77947026 | A | AG | 20 | a0001c0001t0001g0177 a0001c0001t0002g0019 a0001c0001t0002g0020 others(17): Show |
20 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.778-2770dupG | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77947026 | ||||||
chr4:77947026 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(194): Show |
215 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.778-2771A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77947026 | |||||||
chr4:77947189 | A | G | 12 | a0001c0001t0001g0144 a0001c0001t0001g0227 a0001c0001t0001g0232 others(9): Show |
12 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.778-2608A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77947189 | |||||||
chr4:77947224 | C | T | 1 | a0001c0001t0001g0013 | 2 | NA18963.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.778-2573C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77947224 | |||||||
chr4:77947264 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.778-2533A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77947264 | |||||||
chr4:77947273 | T | G | 7 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(4): Show |
7 | HG02280.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-2524T>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77947273 | |||||||
chr4:77947319 | T | C | 5 | a0002c0002t0002g0085 a0002c0002t0002g0089 a0002c0002t0002g0090 others(2): Show |
5 | HG00639.hp1 HG01496.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-2478T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77947319 | |||||||
chr4:77947592 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-2205G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77947592 | |||||||
chr4:77947884 | T | A | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(215): Show |
236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.778-1913T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77947884 | |||||||
chr4:77947934 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.778-1863G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77947934 | |||||||
chr4:77948024 | T | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
235 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.778-1773T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77948024 | |||||||
chr4:77948201 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.778-1596G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77948201 | |||||||
chr4:77948405 | A | T | 7 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(4): Show |
7 | HG02280.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-1392A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77948405 | |||||||
chr4:77948459 | C | G | 1 | a0002c0002t0002g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.778-1338C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77948459 | |||||||
chr4:77948762 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-1035C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77948762 | |||||||
chr4:77948771 | C | CT | 26 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(23): Show |
29 | HG00544.hp1 HG00558.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.778-1010dupT | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77948771 | ||||||
chr4:77948771 | C | CTT | 21 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
21 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-1011_778-1010d others(4): Show |
MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr4 | 77948771 | ||||||
chr4:77948802 | C | G | 1 | a0002c0002t0002g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.778-995C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77948802 | |||||||
chr4:77948856 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.778-941C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77948856 | |||||||
chr4:77948880 | C | T | 7 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(4): Show |
7 | HG02280.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.778-917C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77948880 | |||||||
chr4:77949050 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.778-747C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77949050 | |||||||
chr4:77949293 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.778-504A>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77949293 | |||||||
chr4:77949391 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.778-406A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77949391 | |||||||
chr4:77949482 | G | C | 4 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0121 others(1): Show |
4 | HG02451.hp1 HG03540.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-315G>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77949482 | |||||||
chr4:77949489 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.778-308C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77949489 | |||||||
chr4:77949648 | A | G | 2 | a0001c0001t0001g0209 a0001c0001t0001g0221 |
2 | NA18944.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.778-149A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77949648 | |||||||
chr4:77949749 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.778-48T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77949749 | |||||||
chr4:77949786 | T | A | 95 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(92): Show |
101 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.778-11T>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 7/8 | chr4 | 77949786 | |||||||
chr4:77950015 | G | T | 21 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 others(18): Show |
21 | HG00639.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.859+137G>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77950015 | |||||||
chr4:77950024 | A | G | 7 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(4): Show |
7 | HG02280.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.859+146A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77950024 | |||||||
chr4:77950203 | A | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0170 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.859+325A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77950203 | |||||||
chr4:77950371 | A | G | 1 | a0001c0001t0001g0073 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.859+493A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77950371 | |||||||
chr4:77950414 | C | G | 1 | a0001c0001t0002g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.859+536C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77950414 | |||||||
chr4:77950489 | C | G | 7 | a0001c0001t0002g0021 a0001c0001t0002g0062 a0001c0001t0002g0082 others(4): Show |
7 | HG02280.hp1 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.859+611C>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77950489 | |||||||
chr4:77950693 | A | G | 3 | a0001c0001t0001g0230 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG00280.hp1 HG01071.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.859+815A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77950693 | |||||||
chr4:77950705 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.859+827A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77950705 | |||||||
chr4:77950881 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0168 |
2 | NA18947.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.859+1003T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77950881 | |||||||
chr4:77950956 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.859+1078C>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77950956 | |||||||
chr4:77951214 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.860-1275G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77951214 | |||||||
chr4:77951517 | T | C | 1 | a0001c0001t0001g0022 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.860-972T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77951517 | |||||||
chr4:77951565 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0059 |
3 | HG01928.hp1 HG02004.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.860-924A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77951565 | |||||||
chr4:77952226 | A | T | 1 | a0001c0001t0001g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.860-263A>T | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77952226 | |||||||
chr4:77952341 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0117 others(8): Show |
14 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.860-148G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77952341 | |||||||
chr4:77952348 | T | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0120 a0001c0001t0001g0160 others(2): Show |
6 | HG00423.hp1 HG00438.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.860-141T>C | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77952348 | |||||||
chr4:77952451 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(87): Show |
99 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.860-38A>G | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77952451 | |||||||
chr4:77952475 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(87): Show |
99 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.860-14G>A | MRPL1 | ENSG00000169288.18 | transcript | ENST00000315567.13 | protein_coding | 8/8 | chr4 | 77952475 |