Item | Value |
---|---|
geneid | 389432 |
ensemblid | ENSG00000203727.4 |
hgncid | 21180 |
symbol | SAMD5 |
name | sterile alpha motif domain containing 5 |
refseq_nuc | NM_001030060.3 |
refseq_prot | NP_001025231.1 |
ensembl_nuc | ENST00000367474.2 |
ensembl_prot | ENSP00000356444.1 |
mane_status | MANE Select |
chr | chr6 |
start | 147508690 |
end | 147570021 |
strand | + |
ver | v1.2 |
region | chr6:147508690-147570021 |
region5000 | chr6:147503690-147575021 |
regionname0 | SAMD5_chr6_147508690_147570021 |
regionname5000 | SAMD5_chr6_147503690_147575021 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 173 | 331 | 73 | 71 | 129 | 15 | 41 | 92 | SAMD5_chr6_147503690_147575021 | SAMD5 | MCTNI others(168): Show |
chr6 | 147503690 | 147575021 |
a0002 | 0/0 | 173 | 20 | 0 | 3 | 15 | 1 | 1 | 12 | SAMD5_chr6_147503690_147575021 | SAMD5 | MCTNI others(168): Show |
chr6 | 147503690 | 147575021 |
a0003 | 0/0 | 173 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | MCTNI others(168): Show |
chr6 | 147503690 | 147575021 |
a0004 | 0/0 | 173 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | MCTNI others(168): Show |
chr6 | 147503690 | 147575021 |
a0005 | 0/0 | 173 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | MCTNI others(168): Show |
chr6 | 147503690 | 147575021 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 519 | 215 | 39 | 46 | 98 | 9 | 21 | SAMD5_chr6_147503690_147575021 | SAMD5 | ATGTG others(514): Show |
chr6 | 147503690 | 147575021 | ||
a0001c0002 | 0/0 | 519 | 113 | 33 | 23 | 31 | 6 | 20 | SAMD5_chr6_147503690_147575021 | SAMD5 | ATGTG others(514): Show |
chr6 | 147503690 | 147575021 | ||
a0001c0006 | 0/0 | 519 | 3 | 1 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | ATGTG others(514): Show |
chr6 | 147503690 | 147575021 | ||
a0002c0003 | 0/0 | 519 | 20 | 0 | 3 | 15 | 1 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | ATGTG others(514): Show |
chr6 | 147503690 | 147575021 | ||
a0003c0004 | 0/0 | 519 | 8 | 8 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | ATGTG others(514): Show |
chr6 | 147503690 | 147575021 | ||
a0004c0005 | 0/0 | 519 | 4 | 4 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | ATGTG others(514): Show |
chr6 | 147503690 | 147575021 | ||
a0005c0007 | 0/0 | 519 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | ATGTG others(514): Show |
chr6 | 147503690 | 147575021 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6327 | 38 | 5 | 8 | 19 | 3 | 3 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0002 | 0/0 | 6328 | 26 | 0 | 4 | 21 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0003 | 0/0 | 6327 | 26 | 1 | 3 | 20 | 1 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0005 | 1/0 | 6326 | 25 | 2 | 14 | 3 | 0 | 5 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0006 | 0/0 | 6328 | 16 | 0 | 10 | 1 | 1 | 4 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0009 | 0/0 | 6327 | 11 | 0 | 0 | 11 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0011 | 0/0 | 6327 | 7 | 7 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0012 | 0/0 | 6327 | 6 | 6 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0016 | 0/0 | 6325 | 2 | 1 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0017 | 0/0 | 6328 | 3 | 0 | 0 | 0 | 0 | 3 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0019 | 0/0 | 6327 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0020 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0021 | 0/0 | 6328 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0027 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0028 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0029 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0030 | 0/0 | 6327 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0033 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0035 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGAGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0071 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0072 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0074 | 0/0 | 6325 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0075 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0076 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0078 | 0/0 | 6329 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6324): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0079 | 0/0 | 6329 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6324): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0080 | 0/0 | 6327 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0081 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0082 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0083 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0084 | 0/0 | 6317 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6312): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0085 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0086 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0087 | 0/0 | 6327 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0088 | 0/1 | 6327 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0089 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0090 | 0/0 | 6327 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0091 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0092 | 0/0 | 6327 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0094 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0095 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0096 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0097 | 0/0 | 6326 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0098 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0099 | 0/0 | 6326 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0100 | 0/0 | 6325 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0101 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0102 | 0/0 | 6329 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6324): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0103 | 0/0 | 6328 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0104 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0105 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0106 | 0/0 | 6480 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6475): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0108 | 0/0 | 6326 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0109 | 0/0 | 6326 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0111 | 0/0 | 6329 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6324): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0112 | 0/0 | 6326 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0001t0113 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0004 | 0/0 | 6327 | 25 | 5 | 7 | 8 | 2 | 3 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0007 | 0/0 | 6328 | 13 | 1 | 2 | 9 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0008 | 0/0 | 6327 | 12 | 8 | 2 | 0 | 2 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0010 | 0/0 | 6327 | 9 | 0 | 2 | 5 | 0 | 2 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0013 | 0/0 | 6326 | 4 | 0 | 1 | 2 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0014 | 0/0 | 6326 | 4 | 1 | 1 | 1 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0015 | 0/0 | 6327 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0022 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0023 | 0/0 | 6326 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0024 | 0/0 | 6326 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0025 | 0/0 | 6327 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0026 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0036 | 0/0 | 6326 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0037 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0038 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0039 | 0/0 | 6328 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0040 | 0/0 | 6327 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0041 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0042 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0043 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0044 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0045 | 0/0 | 6329 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6324): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0046 | 0/0 | 6328 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0047 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0048 | 0/0 | 6327 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0049 | 0/0 | 6327 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0050 | 0/0 | 6327 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0051 | 0/0 | 6327 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0052 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0054 | 0/0 | 6326 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0055 | 0/0 | 6326 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0056 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0057 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0058 | 0/0 | 6328 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0059 | 0/0 | 6465 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6460): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0060 | 0/0 | 6326 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0061 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0062 | 0/0 | 6327 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0063 | 0/0 | 6326 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0064 | 0/0 | 6326 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0065 | 0/0 | 6327 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0066 | 0/0 | 6329 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6324): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0067 | 0/0 | 6325 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0068 | 0/0 | 6326 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0069 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0001c0002t0070 | 0/0 | 6328 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0001c0006t0015 | 0/0 | 6327 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0001c0006t0053 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0002c0003t0001 | 0/0 | 6327 | 5 | 0 | 1 | 2 | 1 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0002c0003t0002 | 0/0 | 6328 | 4 | 0 | 1 | 3 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0002c0003t0003 | 0/0 | 6327 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0002c0003t0018 | 0/0 | 6327 | 3 | 0 | 0 | 3 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0002c0003t0031 | 0/0 | 6327 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0002c0003t0032 | 0/0 | 6327 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0002c0003t0033 | 0/0 | 6328 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6323): Show |
chr6 | 147503690 | 147575021 |
a0002c0003t0073 | 0/0 | 6326 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0003c0004t0001 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0003c0004t0016 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0003c0004t0020 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0003c0004t0077 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0003c0004t0093 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0003c0004t0107 | 0/0 | 6326 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6321): Show |
chr6 | 147503690 | 147575021 |
a0003c0004t0110 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0004c0005t0012 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
a0004c0005t0029 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0004c0005t0034 | 0/0 | 6325 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6320): Show |
chr6 | 147503690 | 147575021 |
a0005c0007t0011 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | AGTGC others(6322): Show |
chr6 | 147503690 | 147575021 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0211 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0005g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0002 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0006g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0009g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0011g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0012g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0012g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0012g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0012g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0012g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0016g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0016g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0017g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0017g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0019g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0019g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0019g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0020g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0020g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0021g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0021g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0021g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0027g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0027g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0028g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0028g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0029g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0030g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0030g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0033g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0035g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0071g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0072g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0074g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0075g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0076g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0078g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0079g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0080g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0081g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0082g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0083g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0084g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0085g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0086g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0087g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0088g0325 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0089g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0090g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0091g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0092g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0094g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0095g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0096g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0097g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0098g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0099g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0100g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0101g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0102g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0103g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0104g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0105g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0106g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0108g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0109g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0111g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0112g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0001t0113g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0001 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0008g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0010g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0013g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0013g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0013g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0013g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0014g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0014g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0014g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0015g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0015g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0022g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0022g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0023g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0023g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0024g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0024g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0025g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0025g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0026g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0026g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0036g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0037g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0038g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0039g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0040g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0041g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0042g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0043g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0044g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0045g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0046g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0047g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0048g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0049g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0050g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0051g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0052g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0054g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0055g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0056g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0057g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0058g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0059g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0060g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0061g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0062g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0063g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0064g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0065g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0066g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0067g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0068g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0069g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0002t0070g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0006t0015g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0006t0015g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0001c0006t0053g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0018g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0018g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0031g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0031g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0032g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0032g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0033g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0002c0003t0073g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0016g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0016g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0020g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0077g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0093g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0107g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0003c0004t0110g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0004c0005t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0004c0005t0029g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0004c0005t0034g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0004c0005t0034g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
a0005c0007t0011g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0057 | g0169 | EUR | GBR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00140 | hp2 | a0001 | c0001 | t0016 | g0246 | EUR | GBR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | FIN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00280 | hp2 | a0001 | c0002 | t0004 | g0176 | EUR | FIN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0326 | EUR | FIN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00323 | hp2 | a0002 | c0003 | t0001 | g0021 | EUR | FIN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00408 | hp2 | a0001 | c0001 | t0009 | g0053 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00423 | hp1 | a0001 | c0001 | t0009 | g0331 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00544 | hp1 | a0001 | c0002 | t0007 | g0116 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00609 | hp1 | a0002 | c0003 | t0002 | g0022 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00609 | hp2 | a0001 | c0001 | t0009 | g0039 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00621 | hp2 | a0001 | c0001 | t0019 | g0263 | EAS | CHS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0313 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00639 | hp2 | a0001 | c0002 | t0014 | g0164 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00733 | hp1 | a0001 | c0001 | t0112 | g0254 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00733 | hp2 | a0001 | c0002 | t0054 | g0154 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0323 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0252 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00738 | hp1 | a0001 | c0006 | t0015 | g0141 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0207 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0267 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0308 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01069 | hp2 | a0001 | c0002 | t0004 | g0161 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0307 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01071 | hp2 | a0002 | c0003 | t0001 | g0023 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0295 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01081 | hp1 | a0001 | c0002 | t0046 | g0178 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01081 | hp2 | a0001 | c0006 | t0015 | g0140 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01106 | hp2 | a0001 | c0002 | t0004 | g0148 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0270 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01109 | hp2 | a0001 | c0002 | t0004 | g0083 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01169 | hp1 | a0001 | c0002 | t0004 | g0168 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0235 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01192 | hp1 | a0001 | c0002 | t0004 | g0119 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01192 | hp2 | a0001 | c0001 | t0090 | g0199 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01243 | hp1 | a0002 | c0003 | t0073 | g0020 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0214 | AMR | PUR | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01255 | hp1 | a0001 | c0002 | t0007 | g0105 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01256 | hp1 | a0001 | c0001 | t0005 | g0345 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01256 | hp2 | a0001 | c0001 | t0030 | g0188 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01257 | hp1 | a0001 | c0002 | t0008 | g0110 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0218 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01258 | hp1 | a0001 | c0002 | t0008 | g0111 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01258 | hp2 | a0001 | c0001 | t0030 | g0189 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01261 | hp1 | a0001 | c0002 | t0051 | g0104 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01346 | hp2 | a0001 | c0002 | t0024 | g0162 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0276 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0329 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0330 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0260 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01433 | hp2 | a0001 | c0002 | t0013 | g0106 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0063 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0064 | EUR | IBS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01516 | hp1 | a0001 | c0001 | t0071 | g0212 | EUR | IBS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01516 | hp2 | a0001 | c0002 | t0008 | g0138 | EUR | IBS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01517 | hp2 | a0001 | c0002 | t0008 | g0139 | EUR | IBS | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01884 | hp1 | a0001 | c0001 | t0085 | g0061 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0213 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01891 | hp1 | a0001 | c0002 | t0068 | g0067 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01928 | hp1 | a0002 | c0003 | t0002 | g0026 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01928 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01934 | hp1 | a0001 | c0001 | t0111 | g0013 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01934 | hp2 | a0001 | c0002 | t0049 | g0117 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01943 | hp1 | a0001 | c0001 | t0092 | g0217 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01975 | hp1 | a0001 | c0002 | t0048 | g0001 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01975 | hp2 | a0001 | c0001 | t0097 | g0065 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01978 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01978 | hp2 | a0001 | c0002 | t0004 | g0001 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01981 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01981 | hp2 | a0001 | c0002 | t0010 | g0163 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02004 | hp2 | a0001 | c0002 | t0060 | g0124 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02027 | hp2 | a0001 | c0002 | t0007 | g0147 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02040 | hp1 | a0001 | c0001 | t0109 | g0037 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02040 | hp2 | a0001 | c0001 | t0009 | g0066 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02055 | hp1 | a0001 | c0001 | t0011 | g0221 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02055 | hp2 | a0001 | c0001 | t0020 | g0152 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02056 | hp1 | a0002 | c0003 | t0033 | g0025 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02071 | hp2 | a0001 | c0002 | t0043 | g0158 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02074 | hp2 | a0001 | c0001 | t0009 | g0272 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02129 | hp1 | a0001 | c0001 | t0083 | g0318 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02129 | hp2 | a0001 | c0002 | t0041 | g0128 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02132 | hp1 | a0001 | c0001 | t0033 | g0013 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02132 | hp2 | a0001 | c0001 | t0100 | g0227 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02135 | hp1 | a0001 | c0002 | t0013 | g0137 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02145 | hp1 | a0005 | c0007 | t0011 | g0090 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02145 | hp2 | a0001 | c0006 | t0053 | g0142 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02148 | hp2 | a0001 | c0001 | t0006 | g0328 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0337 | EAS | CDX | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02155 | hp2 | a0001 | c0002 | t0010 | g0145 | EAS | CDX | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02165 | hp1 | a0001 | c0001 | t0091 | g0034 | EAS | CDX | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02165 | hp2 | a0001 | c0001 | t0035 | g0300 | EAS | CDX | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0282 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02273 | hp1 | a0001 | c0002 | t0024 | g0112 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02273 | hp2 | a0001 | c0001 | t0005 | g0311 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02293 | hp1 | a0001 | c0002 | t0007 | g0114 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0002 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02451 | hp1 | a0001 | c0002 | t0004 | g0171 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02451 | hp2 | a0001 | c0002 | t0008 | g0174 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02523 | hp2 | a0001 | c0001 | t0089 | g0044 | EAS | KHV | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02572 | hp1 | a0001 | c0001 | t0011 | g0279 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02572 | hp2 | a0001 | c0001 | t0028 | g0253 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02615 | hp1 | a0003 | c0004 | t0016 | g0072 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02615 | hp2 | a0001 | c0001 | t0099 | g0062 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02622 | hp1 | a0001 | c0001 | t0020 | g0192 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02622 | hp2 | a0001 | c0002 | t0052 | g0095 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02630 | hp1 | a0001 | c0001 | t0012 | g0264 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02630 | hp2 | a0001 | c0002 | t0026 | g0343 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02683 | hp1 | a0001 | c0001 | t0006 | g0249 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02683 | hp2 | a0001 | c0001 | t0098 | g0187 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02698 | hp1 | a0001 | c0001 | t0017 | g0196 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02698 | hp2 | a0001 | c0002 | t0070 | g0143 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02723 | hp1 | a0001 | c0001 | t0011 | g0197 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02723 | hp2 | a0001 | c0001 | t0027 | g0036 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02809 | hp1 | a0001 | c0001 | t0108 | g0059 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02809 | hp2 | a0001 | c0002 | t0015 | g0166 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02818 | hp1 | a0001 | c0002 | t0008 | g0340 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02886 | hp1 | a0001 | c0002 | t0026 | g0087 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02886 | hp2 | a0001 | c0002 | t0015 | g0172 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0010 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02895 | hp2 | a0001 | c0002 | t0004 | g0129 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02896 | hp1 | a0001 | c0001 | t0012 | g0010 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02896 | hp2 | a0004 | c0005 | t0034 | g0047 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02897 | hp1 | a0001 | c0002 | t0004 | g0130 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02897 | hp2 | a0004 | c0005 | t0034 | g0046 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02922 | hp1 | a0001 | c0001 | t0095 | g0074 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02922 | hp2 | a0004 | c0005 | t0029 | g0043 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02965 | hp1 | a0001 | c0001 | t0012 | g0344 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02965 | hp2 | a0003 | c0004 | t0020 | g0077 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02970 | hp1 | a0001 | c0002 | t0069 | g0107 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02970 | hp2 | a0001 | c0001 | t0011 | g0209 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02976 | hp1 | a0001 | c0002 | t0008 | g0181 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02976 | hp2 | a0001 | c0002 | t0004 | g0089 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03017 | hp1 | a0001 | c0002 | t0064 | g0103 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03041 | hp1 | a0001 | c0002 | t0004 | g0084 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03041 | hp2 | a0001 | c0002 | t0008 | g0342 | AFR | GWD | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03098 | hp1 | a0001 | c0001 | t0105 | g0194 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03098 | hp2 | a0001 | c0002 | t0025 | g0341 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03130 | hp1 | a0001 | c0002 | t0014 | g0080 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03130 | hp2 | a0001 | c0002 | t0008 | g0180 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03139 | hp1 | a0001 | c0001 | t0029 | g0144 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03139 | hp2 | a0001 | c0002 | t0022 | g0167 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03195 | hp1 | a0001 | c0002 | t0023 | g0088 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03195 | hp2 | a0003 | c0004 | t0110 | g0070 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03209 | hp1 | a0001 | c0001 | t0104 | g0244 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03209 | hp2 | a0001 | c0002 | t0037 | g0081 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03225 | hp1 | a0003 | c0004 | t0001 | g0068 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03225 | hp2 | a0001 | c0001 | t0012 | g0338 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03239 | hp1 | a0001 | c0002 | t0039 | g0133 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03239 | hp2 | a0001 | c0002 | t0062 | g0121 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0033 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03453 | hp2 | a0001 | c0001 | t0028 | g0297 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03486 | hp1 | a0001 | c0001 | t0016 | g0226 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03486 | hp2 | a0001 | c0001 | t0096 | g0054 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03490 | hp1 | a0001 | c0001 | t0017 | g0007 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0238 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03491 | hp1 | a0001 | c0001 | t0103 | g0241 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0008 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03492 | hp1 | a0001 | c0001 | t0017 | g0007 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0008 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03516 | hp1 | a0001 | c0001 | t0027 | g0245 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | ESN | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03579 | hp1 | a0001 | c0002 | t0022 | g0086 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03579 | hp2 | a0001 | c0002 | t0042 | g0131 | AFR | MSL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03654 | hp1 | a0001 | c0002 | t0065 | g0135 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03654 | hp2 | a0001 | c0002 | t0014 | g0102 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0206 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03669 | hp2 | a0001 | c0002 | t0010 | g0170 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0239 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03710 | hp1 | a0001 | c0002 | t0004 | g0078 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03710 | hp2 | a0001 | c0002 | t0058 | g0126 | SAS | PJL | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03831 | hp1 | a0001 | c0002 | t0066 | g0094 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0336 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03834 | hp1 | a0001 | c0002 | t0013 | g0120 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03927 | hp1 | a0001 | c0002 | t0056 | g0092 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03927 | hp2 | a0001 | c0001 | t0080 | g0201 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG03942 | hp2 | a0001 | c0002 | t0004 | g0127 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04115 | hp1 | a0001 | c0002 | t0040 | g0136 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04115 | hp2 | a0001 | c0002 | t0061 | g0125 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0298 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04184 | hp2 | a0001 | c0002 | t0038 | g0149 | SAS | BEB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0215 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04204 | hp1 | a0001 | c0002 | t0045 | g0091 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04204 | hp2 | a0002 | c0003 | t0001 | g0032 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04228 | hp1 | a0001 | c0002 | t0004 | g0093 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG04228 | hp2 | a0001 | c0002 | t0010 | g0165 | SAS | STU | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18522 | hp1 | a0001 | c0002 | t0059 | g0079 | AFR | YRI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18522 | hp2 | a0001 | c0002 | t0008 | g0179 | AFR | YRI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18612 | hp1 | a0001 | c0001 | t0072 | g0222 | EAS | CHB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18612 | hp2 | a0002 | c0003 | t0003 | g0024 | EAS | CHB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18747 | hp1 | a0001 | c0001 | t0084 | g0288 | EAS | CHB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | CHB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18906 | hp2 | a0001 | c0001 | t0011 | g0281 | AFR | YRI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18943 | hp1 | a0001 | c0001 | t0009 | g0057 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18944 | hp1 | a0001 | c0001 | t0005 | g0322 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18946 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18948 | hp1 | a0001 | c0002 | t0044 | g0098 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18957 | hp1 | a0001 | c0002 | t0063 | g0159 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18957 | hp2 | a0001 | c0001 | t0075 | g0233 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18960 | hp1 | a0001 | c0001 | t0074 | g0327 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18961 | hp1 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18961 | hp2 | a0001 | c0001 | t0009 | g0200 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18963 | hp1 | a0001 | c0002 | t0007 | g0099 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18964 | hp1 | a0001 | c0002 | t0010 | g0097 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18964 | hp2 | a0001 | c0001 | t0082 | g0234 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18965 | hp1 | a0002 | c0003 | t0018 | g0004 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18966 | hp1 | a0001 | c0001 | t0019 | g0040 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18966 | hp2 | a0001 | c0001 | t0086 | g0275 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18968 | hp2 | a0002 | c0003 | t0003 | g0029 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18970 | hp1 | a0001 | c0002 | t0013 | g0123 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18970 | hp2 | a0002 | c0003 | t0031 | g0018 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18974 | hp1 | a0001 | c0002 | t0007 | g0014 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18974 | hp2 | a0001 | c0001 | t0009 | g0259 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18977 | hp1 | a0001 | c0002 | t0007 | g0014 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18980 | hp1 | a0001 | c0002 | t0047 | g0118 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18980 | hp2 | a0001 | c0002 | t0007 | g0156 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18981 | hp2 | a0001 | c0002 | t0004 | g0100 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18982 | hp2 | a0001 | c0001 | t0006 | g0301 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18984 | hp1 | a0001 | c0002 | t0014 | g0003 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18987 | hp1 | a0002 | c0003 | t0002 | g0017 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18987 | hp2 | a0001 | c0002 | t0004 | g0115 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18988 | hp1 | a0001 | c0001 | t0078 | g0321 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18988 | hp2 | a0001 | c0001 | t0019 | g0055 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18990 | hp2 | a0001 | c0001 | t0009 | g0273 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18995 | hp1 | a0001 | c0002 | t0004 | g0109 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18997 | hp1 | a0001 | c0002 | t0010 | g0160 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18997 | hp2 | a0001 | c0001 | t0101 | g0277 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18998 | hp1 | a0001 | c0001 | t0009 | g0292 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA18998 | hp2 | a0001 | c0002 | t0004 | g0108 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19000 | hp1 | a0001 | c0001 | t0021 | g0049 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19001 | hp2 | a0002 | c0003 | t0018 | g0015 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19002 | hp1 | a0001 | c0002 | t0007 | g0157 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19004 | hp1 | a0002 | c0003 | t0032 | g0030 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19010 | hp1 | a0002 | c0003 | t0031 | g0019 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19011 | hp2 | a0002 | c0003 | t0001 | g0016 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19012 | hp1 | a0002 | c0003 | t0018 | g0004 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19030 | hp1 | a0001 | c0001 | t0081 | g0243 | AFR | LWK | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19030 | hp2 | a0001 | c0001 | t0106 | g0058 | AFR | LWK | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19043 | hp2 | a0001 | c0001 | t0011 | g0208 | AFR | LWK | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19054 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19054 | hp2 | a0001 | c0001 | t0102 | g0333 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19057 | hp1 | a0001 | c0001 | t0005 | g0261 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19057 | hp2 | a0001 | c0002 | t0050 | g0146 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19064 | hp1 | a0001 | c0002 | t0004 | g0155 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19070 | hp1 | a0001 | c0002 | t0010 | g0113 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19070 | hp2 | a0001 | c0001 | t0009 | g0271 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19078 | hp1 | a0001 | c0001 | t0005 | g0317 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19078 | hp2 | a0001 | c0001 | t0079 | g0268 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19079 | hp1 | a0001 | c0002 | t0007 | g0122 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19080 | hp1 | a0001 | c0002 | t0004 | g0003 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19083 | hp1 | a0001 | c0001 | t0021 | g0220 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19088 | hp1 | a0001 | c0001 | t0021 | g0262 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19088 | hp2 | a0002 | c0003 | t0002 | g0028 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19090 | hp2 | a0001 | c0002 | t0010 | g0101 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19091 | hp1 | a0001 | c0002 | t0007 | g0096 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19091 | hp2 | a0002 | c0003 | t0032 | g0027 | EAS | JPT | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19240 | hp1 | a0001 | c0002 | t0008 | g0173 | AFR | YRI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA19240 | hp2 | a0001 | c0001 | t0113 | g0151 | AFR | YRI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0216 | AFR | ASW | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20129 | hp2 | a0003 | c0004 | t0016 | g0071 | AFR | ASW | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20752 | hp1 | a0001 | c0001 | t0087 | g0314 | EUR | TSI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20752 | hp2 | a0001 | c0002 | t0067 | g0175 | EUR | TSI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20805 | hp1 | a0001 | c0002 | t0004 | g0001 | EUR | TSI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20805 | hp2 | a0001 | c0001 | t0094 | g0210 | EUR | TSI | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20905 | hp1 | a0001 | c0002 | t0007 | g0134 | SAS | GIH | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA20905 | hp2 | a0001 | c0001 | t0076 | g0193 | SAS | GIH | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01123 | hp1 | a0001 | c0002 | t0010 | g0177 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG01123 | hp2 | a0001 | c0002 | t0004 | g0073 | AMR | CLM | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02109 | hp1 | a0001 | c0002 | t0055 | g0182 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02109 | hp2 | a0003 | c0004 | t0107 | g0069 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02486 | hp1 | a0003 | c0004 | t0093 | g0075 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02486 | hp2 | a0001 | c0002 | t0007 | g0153 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02559 | hp1 | a0001 | c0002 | t0023 | g0082 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG02559 | hp2 | a0001 | c0002 | t0036 | g0132 | AFR | ACB | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG06807 | hp1 | a0004 | c0005 | t0012 | g0048 | AFR | USA | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
HG06807 | hp2 | a0003 | c0004 | t0077 | g0076 | AFR | USA | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA21309 | hp1 | a0001 | c0002 | t0008 | g0150 | AFR | LWK | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
NA21309 | hp2 | a0001 | c0002 | t0025 | g0085 | AFR | LWK | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
homoSapiens | chm13v2 | a0001 | c0001 | t0088 | g0325 | REF | REF | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0211 | REF | REF | SAMD5_chr6_147503690_147575021 | SAMD5 | chr6 | 147503690 | 147575021 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:147509076 | G | C | 1 | a0002 | 20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
missense_variant | MODERATE | c.148G>C | p.Ala50Pro | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 387/6326 | 148/522 | 50/173 | chr6 | 147509076 | |||
chr6:147509088 | C | G | 1 | a0005 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.160C>G | p.Arg54Gly | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 399/6326 | 160/522 | 54/173 | chr6 | 147509088 | |||
chr6:147509167 | C | T | 1 | a0004 | 4 | HG02896.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
missense_variant | MODERATE | c.239C>T | p.Pro80Leu | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 478/6326 | 239/522 | 80/173 | chr6 | 147509167 | |||
chr6:147509172 | C | T | 1 | a0003 | 8 | HG02109.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
missense_variant | MODERATE | c.244C>T | p.Pro82Ser | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 483/6326 | 244/522 | 82/173 | chr6 | 147509172 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:147508937 | C | T | 2 | a0001c0002 a0001c0006 |
116 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(113): Show |
synonymous_variant | LOW | c.9C>T | p.Thr3Thr | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 248/6326 | 9/522 | 3/173 | chr6 | 147508937 | |||
chr6:147509144 | C | G | 1 | a0001c0006 | 3 | HG00738.hp1 HG01081.hp2 HG02145.hp2 |
synonymous_variant | LOW | c.216C>G | p.Leu72Leu | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 455/6326 | 216/522 | 72/173 | chr6 | 147509144 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:147508692 | T | A | 1 | a0001c0001t0035 | 1 | HG02165.hp2 | 5_prime_UTR_variant | MODIFIER | c.-237T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 237 | chr6 | 147508692 | ||||||
chr6:147508708 | T | G | 48 | a0001c0002t0004 a0001c0002t0007 a0001c0002t0008 others(45): Show |
116 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(113): Show |
5_prime_UTR_variant | MODIFIER | c.-221T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 221 | chr6 | 147508708 | ||||||
chr6:147508759 | C | T | 1 | a0001c0001t0113 | 1 | NA19240.hp2 | 5_prime_UTR_variant | MODIFIER | c.-170C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 170 | chr6 | 147508759 | ||||||
chr6:147508783 | C | T | 1 | a0001c0002t0070 | 1 | HG02698.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-146C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | chr6 | 147508783 | |||||||
chr6:147508887 | G | A | 1 | a0001c0001t0071 | 1 | HG01516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 42 | chr6 | 147508887 | ||||||
chr6:147508890 | G | T | 1 | a0001c0002t0069 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/2 | 39 | chr6 | 147508890 | ||||||
chr6:147564658 | G | A | 1 | a0001c0001t0072 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*202G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 202 | chr6 | 147564658 | ||||||
chr6:147564667 | C | T | 34 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0016 others(31): Show |
96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*211C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 211 | chr6 | 147564667 | ||||||
chr6:147564822 | A | T | 5 | a0001c0001t0100 a0001c0001t0101 a0001c0001t0102 others(2): Show |
5 | HG02132.hp2 HG03491.hp1 HG03710.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*366A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 366 | chr6 | 147564822 | ||||||
chr6:147564856 | A | G | 22 | a0001c0001t0011 a0001c0001t0016 a0001c0001t0097 others(19): Show |
43 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*400A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 400 | chr6 | 147564856 | ||||||
chr6:147564971 | C | G | 33 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0020 others(30): Show |
92 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*515C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 515 | chr6 | 147564971 | ||||||
chr6:147565195 | T | C | 1 | a0001c0002t0036 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*739T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 739 | chr6 | 147565195 | ||||||
chr6:147565381 | T | A | 1 | a0001c0001t0105 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*925T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 925 | chr6 | 147565381 | ||||||
chr6:147565456 | T | C | 18 | a0001c0001t0016 a0001c0001t0020 a0001c0001t0027 others(15): Show |
26 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1000T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1000 | chr6 | 147565456 | ||||||
chr6:147565464 | G | GT | 57 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0009 others(54): Show |
201 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*1021dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1022 | INFO_REALIGN_3_PRIME | chr6 | 147565464 | |||||
chr6:147565500 | C | A | 1 | a0003c0004t0107 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1044C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1044 | chr6 | 147565500 | ||||||
chr6:147565545 | G | A | 1 | a0001c0001t0100 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1089G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1089 | chr6 | 147565545 | ||||||
chr6:147565582 | T | C | 58 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0011 others(55): Show |
169 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1126T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1126 | chr6 | 147565582 | ||||||
chr6:147565591 | G | A | 5 | a0001c0001t0009 a0001c0001t0035 a0001c0001t0078 others(2): Show |
15 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1135G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1135 | chr6 | 147565591 | ||||||
chr6:147565684 | T | C | 1 | a0001c0002t0038 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1228T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1228 | chr6 | 147565684 | ||||||
chr6:147565715 | C | T | 2 | a0001c0002t0052 a0003c0004t0093 |
2 | HG02486.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1259C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1259 | chr6 | 147565715 | ||||||
chr6:147565744 | G | A | 1 | a0001c0001t0086 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1288G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1288 | chr6 | 147565744 | ||||||
chr6:147565794 | C | T | 1 | a0001c0001t0100 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1338C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1338 | chr6 | 147565794 | ||||||
chr6:147565862 | T | A | 4 | a0001c0001t0100 a0001c0001t0108 a0001c0002t0061 others(1): Show |
4 | HG02132.hp2 HG02809.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1406T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1406 | chr6 | 147565862 | ||||||
chr6:147565905 | T | C | 7 | a0001c0001t0016 a0001c0001t0087 a0001c0001t0112 others(4): Show |
10 | HG00140.hp2 HG00733.hp1 HG01891.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1449T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1449 | chr6 | 147565905 | ||||||
chr6:147565956 | C | A | 2 | a0001c0001t0097 a0001c0002t0054 |
2 | HG00733.hp2 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1500C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1500 | chr6 | 147565956 | ||||||
chr6:147565991 | A | G | 1 | a0001c0002t0025 | 2 | HG03098.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1535A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1535 | chr6 | 147565991 | ||||||
chr6:147566082 | A | G | 113 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(110): Show |
325 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(322): Show |
3_prime_UTR_variant | MODIFIER | c.*1626A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1626 | chr6 | 147566082 | ||||||
chr6:147566213 | G | A | 5 | a0001c0001t0021 a0001c0001t0071 a0001c0001t0078 others(2): Show |
8 | HG01243.hp1 HG01346.hp2 HG01516.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1757G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1757 | chr6 | 147566213 | ||||||
chr6:147566214 | C | A | 3 | a0001c0001t0017 a0001c0002t0039 a0001c0002t0040 |
5 | HG02698.hp1 HG03239.hp1 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1758C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1758 | chr6 | 147566214 | ||||||
chr6:147566393 | A | C | 1 | a0003c0004t0110 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1937A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1937 | chr6 | 147566393 | ||||||
chr6:147566433 | C | T | 51 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0011 others(48): Show |
160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*1977C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 1977 | chr6 | 147566433 | ||||||
chr6:147566594 | A | G | 1 | a0002c0003t0031 | 2 | NA18970.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2138A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2138 | chr6 | 147566594 | ||||||
chr6:147566754 | G | A | 19 | a0001c0001t0016 a0001c0001t0020 a0001c0001t0027 others(16): Show |
27 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2298G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2298 | chr6 | 147566754 | ||||||
chr6:147566886 | G | A | 113 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(110): Show |
325 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(322): Show |
3_prime_UTR_variant | MODIFIER | c.*2430G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2430 | chr6 | 147566886 | ||||||
chr6:147567095 | G | A | 2 | a0001c0001t0089 a0002c0003t0032 |
3 | HG02523.hp2 NA19004.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2639G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2639 | chr6 | 147567095 | ||||||
chr6:147567187 | G | A | 1 | a0001c0001t0100 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2731G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2731 | chr6 | 147567187 | ||||||
chr6:147567191 | T | G | 1 | a0001c0001t0090 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2735T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2735 | chr6 | 147567191 | ||||||
chr6:147567232 | T | C | 31 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0017 others(28): Show |
90 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2776T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2776 | chr6 | 147567232 | ||||||
chr6:147567358 | A | C | 20 | a0001c0001t0016 a0001c0001t0020 a0001c0001t0027 others(17): Show |
28 | HG00140.hp2 HG00733.hp1 HG00733.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2902A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 2902 | chr6 | 147567358 | ||||||
chr6:147567586 | TTACACCC others(3): Show |
T | 1 | a0001c0001t0084 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3135_*3144delCCCA others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3135 | INFO_REALIGN_3_PRIME | chr6 | 147567586 | |||||
chr6:147567646 | C | T | 1 | a0001c0001t0083 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3190C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3190 | chr6 | 147567646 | ||||||
chr6:147567660 | T | C | 2 | a0001c0001t0098 a0001c0002t0056 |
2 | HG02683.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3204T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3204 | chr6 | 147567660 | ||||||
chr6:147567791 | C | T | 51 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0011 others(48): Show |
160 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*3335C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3335 | chr6 | 147567791 | ||||||
chr6:147567801 | A | G | 40 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0017 others(37): Show |
99 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*3345A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3345 | chr6 | 147567801 | ||||||
chr6:147567808 | G | A | 1 | a0001c0002t0043 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3352G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3352 | chr6 | 147567808 | ||||||
chr6:147567825 | T | C | 1 | a0001c0001t0081 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3369T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3369 | chr6 | 147567825 | ||||||
chr6:147567907 | C | A | 1 | a0004c0005t0034 | 2 | HG02896.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3451C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3451 | chr6 | 147567907 | ||||||
chr6:147567934 | A | G | 4 | a0001c0001t0029 a0001c0002t0042 a0001c0002t0069 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3478A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3478 | chr6 | 147567934 | ||||||
chr6:147567980 | G | T | 7 | a0001c0001t0012 a0001c0001t0090 a0001c0002t0015 others(4): Show |
14 | HG00738.hp1 HG01081.hp2 HG01192.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3524G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3524 | chr6 | 147567980 | ||||||
chr6:147568139 | G | T | 3 | a0001c0001t0076 a0001c0001t0092 a0001c0002t0051 |
3 | HG01261.hp1 HG01943.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3683G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3683 | chr6 | 147568139 | ||||||
chr6:147568172 | T | C | 6 | a0001c0001t0006 a0001c0001t0033 a0001c0002t0062 others(3): Show |
21 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3716T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3716 | chr6 | 147568172 | ||||||
chr6:147568194 | T | A | 1 | a0001c0002t0047 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3738T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3738 | chr6 | 147568194 | ||||||
chr6:147568195 | G | T | 1 | a0001c0002t0025 | 2 | HG03098.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3739G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3739 | chr6 | 147568195 | ||||||
chr6:147568314 | G | A | 1 | a0001c0001t0076 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3858G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 3858 | chr6 | 147568314 | ||||||
chr6:147568580 | G | A | 1 | a0001c0002t0048 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4124G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4124 | chr6 | 147568580 | ||||||
chr6:147568628 | A | G | 1 | a0001c0001t0100 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4172A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4172 | chr6 | 147568628 | ||||||
chr6:147568676 | G | T | 1 | a0001c0001t0089 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4220G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4220 | chr6 | 147568676 | ||||||
chr6:147568791 | T | G | 1 | a0001c0001t0082 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4335T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4335 | chr6 | 147568791 | ||||||
chr6:147569032 | G | A | 2 | a0001c0001t0033 a0002c0003t0033 |
2 | HG02056.hp1 HG02132.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4576G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4576 | chr6 | 147569032 | ||||||
chr6:147569072 | C | CA | 23 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0017 others(20): Show |
82 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*4624dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4625 | INFO_REALIGN_3_PRIME | chr6 | 147569072 | |||||
chr6:147569159 | C | T | 17 | a0001c0001t0016 a0001c0001t0020 a0001c0001t0028 others(14): Show |
23 | HG00140.hp2 HG00733.hp2 HG01891.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4703C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4703 | chr6 | 147569159 | ||||||
chr6:147569206 | G | T | 4 | a0001c0001t0096 a0001c0002t0036 a0001c0002t0046 others(1): Show |
4 | HG01081.hp1 HG02145.hp2 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4750G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4750 | chr6 | 147569206 | ||||||
chr6:147569219 | T | TA | 26 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0017 others(23): Show |
85 | HG00323.hp1 HG00408.hp1 HG00544.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*4779dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4780 | INFO_REALIGN_3_PRIME | chr6 | 147569219 | |||||
chr6:147569219 | TA | T | 8 | a0001c0001t0029 a0001c0001t0074 a0001c0002t0014 others(5): Show |
11 | HG00639.hp2 HG02922.hp2 HG02970.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4779delA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4779 | INFO_REALIGN_3_PRIME | chr6 | 147569219 | |||||
chr6:147569233 | A | G | 2 | a0001c0001t0097 a0001c0002t0054 |
2 | HG00733.hp2 HG01975.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4777A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4777 | chr6 | 147569233 | ||||||
chr6:147569234 | A | G | 18 | a0001c0001t0016 a0001c0001t0020 a0001c0001t0027 others(15): Show |
26 | HG00140.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4778A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4778 | chr6 | 147569234 | ||||||
chr6:147569235 | AG | A | 18 | a0001c0001t0016 a0001c0001t0020 a0001c0001t0027 others(15): Show |
26 | HG00140.hp2 HG01891.hp1 HG02055.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4780delG | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4780 | chr6 | 147569235 | ||||||
chr6:147569285 | A | AGATAATT others(133): Show |
1 | a0001c0002t0059 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4840_*4841insTTTT others(136): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4841 | INFO_REALIGN_3_PRIME | chr6 | 147569285 | |||||
chr6:147569285 | A | AGATAATT others(148): Show |
1 | a0001c0001t0106 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4840_*4841insTTTT others(151): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 4841 | INFO_REALIGN_3_PRIME | chr6 | 147569285 | |||||
chr6:147569471 | A | G | 1 | a0001c0001t0030 | 2 | HG01256.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5015A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5015 | chr6 | 147569471 | ||||||
chr6:147569479 | T | A | 1 | a0001c0002t0049 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5023T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5023 | chr6 | 147569479 | ||||||
chr6:147569686 | T | C | 1 | a0001c0001t0094 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5230T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5230 | chr6 | 147569686 | ||||||
chr6:147569696 | A | G | 1 | a0001c0001t0080 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5240A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5240 | chr6 | 147569696 | ||||||
chr6:147569844 | A | G | 1 | a0001c0001t0084 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5388A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5388 | chr6 | 147569844 | ||||||
chr6:147569889 | A | T | 2 | a0001c0001t0019 a0001c0002t0050 |
4 | HG00621.hp2 NA18966.hp1 NA18988.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5433A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5433 | chr6 | 147569889 | ||||||
chr6:147569933 | G | A | 1 | a0001c0002t0045 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5477G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 2/2 | 5477 | chr6 | 147569933 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:147509565 | G | C | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+178G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147509565 | |||||||
chr6:147509614 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.459+227T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147509614 | |||||||
chr6:147509694 | A | G | 1 | a0001c0002t0007g0014 | 2 | NA18974.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.459+307A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147509694 | |||||||
chr6:147509856 | A | G | 1 | a0001c0001t0005g0345 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.459+469A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147509856 | |||||||
chr6:147509873 | T | C | 30 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(27): Show |
33 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.459+486T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147509873 | |||||||
chr6:147509925 | A | G | 29 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0052 others(26): Show |
31 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.459+538A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147509925 | |||||||
chr6:147510146 | G | A | 32 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0052 others(29): Show |
34 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.459+759G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510146 | |||||||
chr6:147510230 | T | A | 1 | a0001c0001t0005g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.459+843T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510230 | |||||||
chr6:147510332 | T | C | 28 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0052 others(25): Show |
30 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.459+945T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510332 | |||||||
chr6:147510341 | C | A | 2 | a0001c0001t0003g0064 a0001c0001t0097g0065 |
2 | HG01515.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.459+954C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510341 | |||||||
chr6:147510508 | A | C | 4 | a0001c0002t0008g0340 a0001c0002t0008g0342 a0001c0002t0025g0341 others(1): Show |
4 | HG02630.hp2 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+1121A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510508 | |||||||
chr6:147510710 | G | A | 1 | a0001c0001t0009g0066 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.459+1323G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510710 | |||||||
chr6:147510856 | G | A | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+1469G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510856 | |||||||
chr6:147510933 | G | A | 1 | a0001c0002t0068g0067 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.459+1546G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147510933 | |||||||
chr6:147511020 | G | A | 178 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(175): Show |
186 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.459+1633G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511020 | |||||||
chr6:147511030 | G | T | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.459+1643G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511030 | |||||||
chr6:147511226 | A | G | 124 | a0001c0001t0001g0005 a0001c0001t0002g0337 a0001c0001t0012g0033 others(121): Show |
129 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.459+1839A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511226 | |||||||
chr6:147511308 | C | T | 54 | a0001c0001t0001g0291 a0001c0001t0001g0293 a0001c0001t0001g0294 others(51): Show |
59 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.459+1921C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511308 | |||||||
chr6:147511365 | G | T | 2 | a0001c0001t0106g0058 a0001c0001t0108g0059 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.459+1978G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511365 | |||||||
chr6:147511390 | A | G | 21 | a0001c0002t0004g0168 a0001c0002t0004g0171 a0001c0002t0004g0176 others(18): Show |
21 | HG00140.hp1 HG00280.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.459+2003A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511390 | |||||||
chr6:147511452 | T | C | 1 | a0001c0001t0091g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.459+2065T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511452 | |||||||
chr6:147511502 | T | G | 1 | a0001c0001t0001g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.459+2115T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511502 | |||||||
chr6:147511612 | C | T | 1 | a0001c0001t0012g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.459+2225C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511612 | |||||||
chr6:147511627 | CA | C | 171 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(168): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+2254delA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147511627 | ||||||
chr6:147511840 | T | A | 1 | a0001c0002t0004g0078 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.459+2453T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147511840 | |||||||
chr6:147512102 | C | T | 8 | a0003c0004t0001g0068 a0003c0004t0016g0071 a0003c0004t0016g0072 others(5): Show |
8 | HG02109.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+2715C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512102 | |||||||
chr6:147512146 | C | T | 1 | a0001c0002t0010g0165 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.459+2759C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512146 | |||||||
chr6:147512173 | A | G | 180 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(177): Show |
188 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.459+2786A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512173 | |||||||
chr6:147512245 | C | T | 108 | a0001c0001t0003g0336 a0001c0001t0012g0338 a0001c0001t0020g0152 others(105): Show |
112 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.459+2858C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512245 | |||||||
chr6:147512277 | G | A | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+2890G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512277 | |||||||
chr6:147512713 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.459+3326A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512713 | |||||||
chr6:147512756 | T | C | 2 | a0001c0001t0001g0291 a0001c0001t0002g0290 |
2 | HG00423.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.459+3369T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512756 | |||||||
chr6:147512888 | A | G | 1 | a0001c0001t0002g0337 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.459+3501A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147512888 | |||||||
chr6:147513194 | T | C | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+3807T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513194 | |||||||
chr6:147513269 | T | C | 2 | a0002c0003t0018g0004 a0002c0003t0018g0015 |
3 | NA18965.hp1 NA19001.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.459+3882T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513269 | |||||||
chr6:147513301 | C | T | 28 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0052 others(25): Show |
30 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.459+3914C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513301 | |||||||
chr6:147513513 | G | C | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+4126G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513513 | |||||||
chr6:147513604 | C | G | 1 | a0002c0003t0001g0032 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.459+4217C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513604 | |||||||
chr6:147513691 | A | G | 128 | a0001c0001t0001g0005 a0001c0001t0012g0033 a0001c0001t0012g0338 others(125): Show |
133 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.459+4304A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513691 | |||||||
chr6:147513733 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.459+4346G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513733 | |||||||
chr6:147513981 | T | C | 1 | a0001c0002t0004g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.459+4594T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147513981 | |||||||
chr6:147514002 | C | T | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+4615C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514002 | |||||||
chr6:147514204 | C | T | 7 | a0001c0001t0001g0283 a0001c0001t0002g0286 a0001c0001t0002g0289 others(4): Show |
7 | HG00558.hp1 NA18747.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.459+4817C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514204 | |||||||
chr6:147514211 | G | T | 1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4824G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514211 | |||||||
chr6:147514216 | T | G | 1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4829T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514216 | |||||||
chr6:147514219 | C | G | 1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4832C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514219 | |||||||
chr6:147514223 | T | G | 1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4836T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514223 | |||||||
chr6:147514227 | T | G | 1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4840T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514227 | |||||||
chr6:147514228 | A | G | 1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4841A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514228 | |||||||
chr6:147514229 | G | GGCGGGGG others(22): Show |
1 | a0001c0002t0014g0164 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.459+4842_459+4843i others(31): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514229 | |||||||
chr6:147514415 | GTGGGATC others(50): Show |
G | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+5032_459+5088d others(59): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147514415 | ||||||
chr6:147514419 | G | A | 178 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(175): Show |
186 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.459+5032G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514419 | |||||||
chr6:147514513 | C | T | 3 | a0001c0002t0004g0161 a0001c0002t0010g0163 a0001c0002t0024g0162 |
3 | HG01069.hp2 HG01346.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.459+5126C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514513 | |||||||
chr6:147514532 | C | T | 5 | a0002c0003t0001g0031 a0002c0003t0002g0028 a0002c0003t0003g0029 others(2): Show |
5 | NA18961.hp1 NA18968.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+5145C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514532 | |||||||
chr6:147514788 | C | G | 2 | a0001c0001t0011g0281 a0001c0001t0011g0282 |
2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.459+5401C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514788 | |||||||
chr6:147514789 | G | A | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+5402G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514789 | |||||||
chr6:147514799 | T | C | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+5412T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514799 | |||||||
chr6:147514852 | G | A | 153 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(150): Show |
159 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.459+5465G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514852 | |||||||
chr6:147514862 | C | T | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+5475C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147514862 | |||||||
chr6:147515061 | C | A | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+5674C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515061 | |||||||
chr6:147515081 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.459+5694C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515081 | |||||||
chr6:147515082 | G | A | 153 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(150): Show |
159 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.459+5695G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515082 | |||||||
chr6:147515146 | C | G | 153 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(150): Show |
159 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.459+5759C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515146 | |||||||
chr6:147515176 | G | GT | 50 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0251 others(47): Show |
55 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.459+5820dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | ||||||
chr6:147515176 | G | GTT | 17 | a0001c0001t0001g0274 a0001c0001t0002g0269 a0001c0001t0002g0335 others(14): Show |
17 | HG00609.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.459+5819_459+5820d others(4): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | ||||||
chr6:147515176 | G | GTTTT | 6 | a0001c0001t0003g0278 a0001c0001t0011g0279 a0001c0001t0101g0277 others(3): Show |
6 | HG01106.hp1 HG01928.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+5817_459+5820d others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | ||||||
chr6:147515176 | GTTTTTTT others(1): Show |
G | 31 | a0001c0001t0001g0005 a0001c0001t0002g0056 a0001c0001t0009g0057 others(28): Show |
33 | HG01106.hp2 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.459+5813_459+5820d others(10): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | ||||||
chr6:147515176 | GTTTTTTT others(2): Show |
G | 117 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0052 others(114): Show |
122 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.459+5812_459+5820d others(11): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | ||||||
chr6:147515176 | GTTTTTTT others(3): Show |
G | 2 | a0001c0002t0004g0161 a0001c0002t0045g0091 |
2 | HG01069.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.459+5811_459+5820d others(12): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | ||||||
chr6:147515176 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+5810_459+5820d others(13): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | ||||||
chr6:147515176 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0012g0338 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.459+5804_459+5820d others(19): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515176 | ||||||
chr6:147515188 | T | C | 1 | a0005c0007t0011g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.459+5801T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515188 | |||||||
chr6:147515275 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.459+5888G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515275 | |||||||
chr6:147515362 | C | T | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+5975C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515362 | |||||||
chr6:147515410 | TATCC | T | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+6028_459+6031d others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515410 | ||||||
chr6:147515431 | A | ACCAT | 25 | a0001c0001t0001g0185 a0001c0001t0001g0190 a0001c0001t0001g0247 others(22): Show |
26 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.459+6085_459+6088d others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515431 | ||||||
chr6:147515431 | ACCAT | A | 108 | a0001c0001t0009g0053 a0001c0001t0011g0281 a0001c0001t0011g0282 others(105): Show |
112 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.459+6085_459+6088d others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515431 | ||||||
chr6:147515431 | ACCATCCA others(1): Show |
A | 11 | a0001c0001t0001g0005 a0001c0002t0004g0083 a0001c0002t0004g0084 others(8): Show |
12 | HG01109.hp2 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.459+6081_459+6088d others(10): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515431 | ||||||
chr6:147515431 | ACCATCCA others(5): Show |
A | 1 | a0001c0001t0012g0344 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.459+6077_459+6088d others(14): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515431 | ||||||
chr6:147515431 | ACCATCCA others(9): Show |
A | 4 | a0001c0002t0068g0067 a0003c0004t0016g0071 a0003c0004t0016g0072 others(1): Show |
4 | HG01891.hp1 HG02615.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+6073_459+6088d others(18): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515431 | ||||||
chr6:147515576 | C | G | 2 | a0001c0001t0001g0242 a0001c0001t0079g0268 |
2 | NA19010.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.459+6189C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515576 | |||||||
chr6:147515656 | GC | G | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+6272delC | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147515656 | ||||||
chr6:147515703 | C | T | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+6316C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515703 | |||||||
chr6:147515727 | G | A | 153 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(150): Show |
159 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.459+6340G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515727 | |||||||
chr6:147515921 | T | A | 1 | a0001c0002t0004g0073 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.459+6534T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515921 | |||||||
chr6:147515989 | A | G | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+6602A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147515989 | |||||||
chr6:147516062 | C | G | 153 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(150): Show |
159 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.459+6675C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516062 | |||||||
chr6:147516079 | T | C | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+6692T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516079 | |||||||
chr6:147516202 | C | T | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+6815C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516202 | |||||||
chr6:147516279 | T | C | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+6892T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516279 | |||||||
chr6:147516366 | C | T | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+6979C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516366 | |||||||
chr6:147516383 | C | A | 3 | a0001c0001t0001g0191 a0001c0001t0001g0248 a0001c0001t0005g0008 |
4 | HG00642.hp2 HG00741.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+6996C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516383 | |||||||
chr6:147516397 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0003c0004t0020g0077 others(2): Show |
5 | HG02486.hp1 HG02965.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+7010C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516397 | |||||||
chr6:147516425 | C | G | 4 | a0001c0001t0002g0334 a0001c0001t0003g0320 a0001c0001t0003g0332 others(1): Show |
4 | NA18946.hp2 NA19054.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+7038C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516425 | |||||||
chr6:147516457 | A | C | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+7070A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516457 | |||||||
chr6:147516467 | A | G | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7080A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516467 | |||||||
chr6:147516470 | A | G | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7083A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516470 | |||||||
chr6:147516475 | G | A | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7088G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516475 | |||||||
chr6:147516517 | T | C | 115 | a0001c0001t0001g0005 a0001c0001t0012g0033 a0001c0001t0012g0338 others(112): Show |
119 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.459+7130T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516517 | |||||||
chr6:147516532 | T | A | 4 | a0001c0001t0002g0334 a0001c0001t0003g0320 a0001c0001t0003g0332 others(1): Show |
4 | NA18946.hp2 NA19054.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+7145T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516532 | |||||||
chr6:147516555 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.459+7168A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516555 | |||||||
chr6:147516594 | A | G | 1 | a0001c0002t0010g0165 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.459+7207A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516594 | |||||||
chr6:147516644 | G | A | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7257G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516644 | |||||||
chr6:147516756 | C | T | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7369C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516756 | |||||||
chr6:147516762 | A | T | 1 | a0001c0001t0002g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.459+7375A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516762 | |||||||
chr6:147516791 | C | T | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+7404C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516791 | |||||||
chr6:147516861 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.459+7474C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516861 | |||||||
chr6:147516888 | C | T | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+7501C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147516888 | |||||||
chr6:147517046 | G | A | 36 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0052 others(33): Show |
38 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.459+7659G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517046 | |||||||
chr6:147517057 | T | G | 1 | a0001c0001t0029g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.459+7670T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517057 | |||||||
chr6:147517133 | C | T | 1 | a0001c0001t0009g0057 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.459+7746C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517133 | |||||||
chr6:147517236 | T | C | 1 | a0001c0001t0006g0249 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.459+7849T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517236 | |||||||
chr6:147517279 | G | A | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7892G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517279 | |||||||
chr6:147517345 | G | A | 1 | a0001c0001t0005g0063 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.459+7958G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517345 | |||||||
chr6:147517370 | G | A | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+7983G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517370 | |||||||
chr6:147517409 | G | C | 2 | a0001c0001t0006g0295 a0001c0001t0006g0323 |
2 | HG00735.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.459+8022G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517409 | |||||||
chr6:147517426 | C | T | 1 | a0001c0001t0001g0294 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.459+8039C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517426 | |||||||
chr6:147517492 | G | C | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+8105G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517492 | |||||||
chr6:147517502 | T | TGATAAAT others(8): Show |
172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+8118_459+8119i others(17): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147517502 | ||||||
chr6:147517542 | C | T | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+8155C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517542 | |||||||
chr6:147517562 | C | A | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+8175C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517562 | |||||||
chr6:147517598 | A | C | 28 | a0001c0001t0001g0038 a0001c0001t0001g0051 a0001c0001t0001g0052 others(25): Show |
30 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.459+8211A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517598 | |||||||
chr6:147517600 | T | C | 1 | a0001c0002t0057g0169 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.459+8213T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517600 | |||||||
chr6:147517728 | G | A | 2 | a0001c0001t0011g0281 a0001c0001t0011g0282 |
2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.459+8341G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517728 | |||||||
chr6:147517742 | A | G | 1 | a0001c0002t0023g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.459+8355A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517742 | |||||||
chr6:147517742 | A | T | 1 | a0001c0002t0070g0143 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.459+8355A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517742 | |||||||
chr6:147517780 | A | C | 1 | a0001c0001t0002g0319 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.459+8393A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517780 | |||||||
chr6:147517873 | G | GT | 9 | a0001c0001t0002g0056 a0001c0001t0079g0268 a0001c0002t0007g0153 others(6): Show |
9 | HG00738.hp1 HG01081.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.459+8498dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147517873 | ||||||
chr6:147517897 | T | C | 1 | a0001c0001t0012g0344 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.459+8510T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517897 | |||||||
chr6:147517991 | A | G | 11 | a0001c0002t0004g0083 a0001c0002t0004g0084 a0001c0002t0014g0080 others(8): Show |
11 | HG01109.hp2 HG01891.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.459+8604A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147517991 | |||||||
chr6:147518039 | A | G | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+8652A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518039 | |||||||
chr6:147518168 | C | T | 2 | a0001c0001t0005g0267 a0001c0001t0103g0241 |
2 | HG00741.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.459+8781C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518168 | |||||||
chr6:147518199 | C | T | 1 | a0001c0001t0002g0337 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.459+8812C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518199 | |||||||
chr6:147518244 | A | C | 1 | a0001c0001t0003g0287 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.459+8857A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518244 | |||||||
chr6:147518369 | C | A | 1 | a0001c0001t0001g0291 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.459+8982C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518369 | |||||||
chr6:147518543 | G | A | 1 | a0003c0004t0001g0068 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.459+9156G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518543 | |||||||
chr6:147518555 | G | A | 171 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(168): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.459+9168G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518555 | |||||||
chr6:147518572 | T | G | 1 | a0001c0001t0003g0186 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.459+9185T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518572 | |||||||
chr6:147518613 | C | T | 172 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(169): Show |
179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.459+9226C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518613 | |||||||
chr6:147518638 | G | A | 171 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0051 others(168): Show |
178 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.459+9251G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518638 | |||||||
chr6:147518966 | A | C | 3 | a0003c0004t0020g0077 a0003c0004t0077g0076 a0003c0004t0093g0075 |
3 | HG02486.hp1 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.459+9579A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147518966 | |||||||
chr6:147519443 | A | C | 1 | a0001c0001t0083g0318 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.459+10056A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519443 | |||||||
chr6:147519459 | T | G | 108 | a0001c0001t0001g0038 a0001c0001t0012g0338 a0001c0001t0020g0192 others(105): Show |
111 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.459+10072T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519459 | |||||||
chr6:147519480 | C | G | 1 | a0001c0001t0012g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.459+10093C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519480 | |||||||
chr6:147519609 | T | C | 1 | a0001c0002t0010g0145 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.459+10222T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519609 | |||||||
chr6:147519660 | A | G | 31 | a0001c0001t0003g0060 a0001c0001t0012g0344 a0001c0002t0023g0088 others(28): Show |
32 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.459+10273A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519660 | |||||||
chr6:147519717 | G | T | 1 | a0001c0001t0029g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.459+10330G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519717 | |||||||
chr6:147519800 | A | T | 1 | a0001c0001t0011g0279 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.459+10413A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519800 | |||||||
chr6:147519897 | C | T | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+10510C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519897 | |||||||
chr6:147519949 | C | T | 28 | a0001c0001t0003g0060 a0001c0001t0012g0344 a0002c0003t0001g0016 others(25): Show |
29 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+10562C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147519949 | |||||||
chr6:147520117 | G | GT | 31 | a0001c0001t0001g0248 a0001c0001t0002g0334 a0001c0001t0003g0285 others(28): Show |
32 | HG00323.hp2 HG00423.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.459+10747dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147520117 | ||||||
chr6:147520117 | G | GTT | 124 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(121): Show |
130 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.459+10746_459+1074 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147520117 | ||||||
chr6:147520117 | G | GTTT | 10 | a0001c0001t0009g0057 a0001c0001t0012g0338 a0001c0001t0020g0192 others(7): Show |
10 | HG00738.hp1 HG01081.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.459+10745_459+1074 others(7): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147520117 | ||||||
chr6:147520117 | GT | G | 10 | a0001c0001t0003g0060 a0001c0001t0009g0292 a0001c0001t0012g0344 others(7): Show |
10 | HG02109.hp2 HG02615.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.459+10747delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147520117 | ||||||
chr6:147520139 | A | G | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+10752A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520139 | |||||||
chr6:147520196 | C | A | 1 | a0001c0001t0096g0054 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.459+10809C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520196 | |||||||
chr6:147520220 | C | T | 7 | a0001c0002t0004g0083 a0001c0002t0004g0084 a0001c0002t0014g0080 others(4): Show |
7 | HG01109.hp2 HG02559.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+10833C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520220 | |||||||
chr6:147520377 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.459+10990C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520377 | |||||||
chr6:147520517 | G | C | 4 | a0001c0001t0001g0324 a0001c0001t0002g0335 a0001c0001t0003g0296 others(1): Show |
4 | NA18963.hp2 NA18988.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+11130G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520517 | |||||||
chr6:147520625 | A | C | 158 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(155): Show |
165 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.459+11238A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520625 | |||||||
chr6:147520625 | A | G | 2 | a0001c0001t0005g0238 a0001c0001t0005g0239 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.459+11238A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520625 | |||||||
chr6:147520747 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.459+11360A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520747 | |||||||
chr6:147520788 | T | A | 1 | a0001c0002t0050g0146 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.459+11401T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520788 | |||||||
chr6:147520915 | G | A | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+11528G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147520915 | |||||||
chr6:147521049 | T | C | 27 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0002g0006 others(24): Show |
29 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+11662T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521049 | |||||||
chr6:147521123 | A | G | 1 | a0005c0007t0011g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.459+11736A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521123 | |||||||
chr6:147521135 | TA | T | 27 | a0001c0001t0012g0344 a0002c0003t0001g0016 a0002c0003t0001g0021 others(24): Show |
28 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.459+11749delA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521135 | |||||||
chr6:147521136 | A | T | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+11749A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521136 | |||||||
chr6:147521151 | G | T | 1 | a0001c0002t0040g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.459+11764G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521151 | |||||||
chr6:147521161 | C | T | 2 | a0001c0001t0020g0152 a0001c0001t0113g0151 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.459+11774C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521161 | |||||||
chr6:147521163 | T | C | 1 | a0001c0001t0001g0005 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.459+11776T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521163 | |||||||
chr6:147521469 | A | G | 1 | a0001c0001t0001g0005 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.459+12082A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521469 | |||||||
chr6:147521775 | T | A | 1 | a0001c0001t0005g0317 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.459+12388T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521775 | |||||||
chr6:147521868 | C | CT | 107 | a0001c0001t0005g0063 a0001c0001t0012g0338 a0001c0001t0020g0192 others(104): Show |
110 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.459+12488dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147521868 | ||||||
chr6:147521882 | A | G | 8 | a0001c0001t0012g0344 a0003c0004t0001g0068 a0003c0004t0016g0071 others(5): Show |
8 | HG02109.hp2 HG02615.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.459+12495A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521882 | |||||||
chr6:147521889 | T | G | 27 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0002g0006 others(24): Show |
29 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.459+12502T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521889 | |||||||
chr6:147521983 | C | A | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+12596C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147521983 | |||||||
chr6:147522029 | C | T | 111 | a0001c0001t0005g0063 a0001c0001t0012g0338 a0001c0001t0020g0192 others(108): Show |
114 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.459+12642C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522029 | |||||||
chr6:147522326 | C | T | 2 | a0001c0001t0020g0152 a0001c0001t0113g0151 |
2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.459+12939C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522326 | |||||||
chr6:147522422 | C | A | 1 | a0001c0001t0076g0193 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.459+13035C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522422 | |||||||
chr6:147522537 | G | A | 3 | a0003c0004t0016g0071 a0003c0004t0016g0072 a0003c0004t0110g0070 |
3 | HG02615.hp1 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.459+13150G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522537 | |||||||
chr6:147522614 | C | G | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+13227C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522614 | |||||||
chr6:147522621 | C | T | 5 | a0001c0002t0008g0179 a0001c0002t0008g0180 a0001c0002t0008g0181 others(2): Show |
5 | HG01081.hp1 HG02109.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+13234C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522621 | |||||||
chr6:147522720 | A | G | 113 | a0001c0001t0001g0185 a0001c0001t0001g0247 a0001c0001t0003g0284 others(110): Show |
116 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.459+13333A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522720 | |||||||
chr6:147522799 | A | G | 163 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(160): Show |
170 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.459+13412A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522799 | |||||||
chr6:147522870 | G | C | 2 | a0001c0001t0011g0279 a0001c0001t0105g0194 |
2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.459+13483G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522870 | |||||||
chr6:147522920 | G | A | 2 | a0001c0002t0052g0095 a0003c0004t0093g0075 |
2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.459+13533G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147522920 | |||||||
chr6:147523013 | A | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG01074.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.459+13626A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523013 | |||||||
chr6:147523058 | C | G | 3 | a0001c0001t0003g0060 a0001c0001t0085g0061 a0001c0001t0099g0062 |
3 | HG01884.hp1 HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.459+13671C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523058 | |||||||
chr6:147523091 | C | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0240 |
2 | NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.459+13704C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523091 | |||||||
chr6:147523091 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.459+13704C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523091 | |||||||
chr6:147523117 | C | T | 1 | a0001c0002t0065g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.459+13730C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523117 | |||||||
chr6:147523123 | C | A | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+13736C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523123 | |||||||
chr6:147523142 | C | G | 2 | a0001c0001t0002g0315 a0001c0001t0003g0316 |
2 | NA18965.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.459+13755C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523142 | |||||||
chr6:147523155 | T | C | 2 | a0001c0001t0005g0267 a0001c0001t0103g0241 |
2 | HG00741.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.459+13768T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523155 | |||||||
chr6:147523295 | A | G | 1 | a0001c0001t0005g0235 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.459+13908A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523295 | |||||||
chr6:147523538 | A | G | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.459+14151A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523538 | |||||||
chr6:147523747 | C | T | 122 | a0001c0001t0005g0063 a0001c0001t0020g0192 a0001c0001t0027g0036 others(119): Show |
126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.459+14360C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523747 | |||||||
chr6:147523778 | G | T | 1 | a0001c0001t0082g0234 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.459+14391G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523778 | |||||||
chr6:147523863 | C | T | 18 | a0001c0001t0003g0060 a0001c0001t0011g0279 a0001c0001t0011g0281 others(15): Show |
18 | HG01109.hp2 HG02055.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.459+14476C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523863 | |||||||
chr6:147523864 | G | A | 1 | a0005c0007t0011g0090 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.459+14477G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147523864 | |||||||
chr6:147524170 | C | T | 155 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0002g0006 others(152): Show |
161 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.459+14783C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524170 | |||||||
chr6:147524242 | C | A | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+14855C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524242 | |||||||
chr6:147524252 | G | C | 153 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0002g0006 others(150): Show |
158 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.459+14865G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524252 | |||||||
chr6:147524419 | G | GT | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+15034dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147524419 | ||||||
chr6:147524422 | G | GT | 26 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0002g0006 others(23): Show |
28 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.459+15047dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147524422 | ||||||
chr6:147524422 | G | T | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+15035G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524422 | |||||||
chr6:147524480 | C | T | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+15093C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524480 | |||||||
chr6:147524540 | ACTT | A | 4 | a0001c0001t0011g0279 a0001c0001t0020g0152 a0001c0001t0105g0194 others(1): Show |
4 | HG02055.hp2 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+15161_459+1516 others(7): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147524540 | ||||||
chr6:147524563 | G | A | 2 | a0001c0002t0008g0138 a0001c0002t0008g0139 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.459+15176G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524563 | |||||||
chr6:147524637 | A | C | 153 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0002g0006 others(150): Show |
159 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.459+15250A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524637 | |||||||
chr6:147524690 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.459+15303C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147524690 | |||||||
chr6:147525025 | G | A | 24 | a0001c0001t0012g0344 a0002c0003t0001g0016 a0002c0003t0001g0021 others(21): Show |
25 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.459+15638G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525025 | |||||||
chr6:147525111 | A | G | 162 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0185 others(159): Show |
168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.459+15724A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525111 | |||||||
chr6:147525439 | A | G | 182 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(179): Show |
189 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.459+16052A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525439 | |||||||
chr6:147525513 | C | T | 1 | a0001c0001t0003g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.459+16126C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525513 | |||||||
chr6:147525624 | G | A | 6 | a0001c0002t0007g0096 a0001c0002t0007g0099 a0001c0002t0007g0147 others(3): Show |
6 | HG02027.hp2 HG02135.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+16237G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525624 | |||||||
chr6:147525933 | A | G | 3 | a0003c0004t0020g0077 a0003c0004t0077g0076 a0003c0004t0107g0069 |
3 | HG02109.hp2 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.459+16546A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525933 | |||||||
chr6:147525965 | G | T | 19 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0023 others(16): Show |
20 | HG00323.hp2 HG00609.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.459+16578G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147525965 | |||||||
chr6:147526024 | A | C | 2 | a0002c0003t0001g0023 a0002c0003t0073g0020 |
2 | HG01071.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.459+16637A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526024 | |||||||
chr6:147526099 | G | A | 1 | a0001c0001t0098g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.459+16712G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526099 | |||||||
chr6:147526240 | A | G | 8 | a0001c0001t0002g0230 a0001c0001t0002g0232 a0001c0001t0002g0265 others(5): Show |
8 | HG00558.hp2 HG00597.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+16853A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526240 | |||||||
chr6:147526254 | C | T | 1 | a0001c0002t0025g0341 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.459+16867C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526254 | |||||||
chr6:147526279 | T | C | 1 | a0001c0001t0017g0196 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.459+16892T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526279 | |||||||
chr6:147526387 | C | T | 148 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(145): Show |
154 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.459+17000C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526387 | |||||||
chr6:147526416 | T | C | 19 | a0001c0001t0027g0036 a0001c0001t0085g0061 a0001c0001t0099g0062 others(16): Show |
19 | HG01081.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.459+17029T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526416 | |||||||
chr6:147526453 | A | G | 16 | a0002c0003t0001g0016 a0002c0003t0001g0021 a0002c0003t0001g0031 others(13): Show |
17 | HG00323.hp2 HG00609.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.459+17066A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526453 | |||||||
chr6:147526466 | C | T | 1 | a0001c0001t0099g0062 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.459+17079C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526466 | |||||||
chr6:147526533 | T | C | 7 | a0001c0002t0004g0161 a0001c0002t0007g0105 a0001c0002t0007g0153 others(4): Show |
7 | HG01069.hp2 HG01243.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+17146T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526533 | |||||||
chr6:147526562 | G | A | 17 | a0001c0001t0002g0337 a0002c0003t0001g0016 a0002c0003t0001g0021 others(14): Show |
18 | HG00323.hp2 HG00609.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.459+17175G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526562 | |||||||
chr6:147526582 | G | A | 77 | a0001c0001t0001g0038 a0001c0001t0001g0251 a0001c0001t0002g0250 others(74): Show |
80 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.459+17195G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526582 | |||||||
chr6:147526610 | T | C | 1 | a0001c0001t0029g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.459+17223T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526610 | |||||||
chr6:147526752 | C | A | 6 | a0001c0001t0002g0337 a0002c0003t0001g0016 a0002c0003t0002g0017 others(3): Show |
7 | HG02155.hp1 NA18612.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+17365C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526752 | |||||||
chr6:147526770 | C | T | 1 | a0001c0002t0041g0128 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.459+17383C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526770 | |||||||
chr6:147526803 | C | T | 1 | a0002c0003t0001g0032 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.459+17416C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526803 | |||||||
chr6:147526819 | G | GACAGTAG others(11): Show |
18 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0190 others(15): Show |
20 | HG00323.hp2 HG01074.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.459+17433_459+1743 others(22): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147526819 | ||||||
chr6:147526855 | A | C | 10 | a0001c0001t0002g0337 a0001c0001t0100g0227 a0002c0003t0001g0016 others(7): Show |
11 | HG00323.hp2 HG02056.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.459+17468A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147526855 | |||||||
chr6:147527082 | T | C | 38 | a0001c0001t0001g0038 a0001c0001t0003g0255 a0001c0001t0003g0336 others(35): Show |
38 | HG00733.hp1 HG01109.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.459+17695T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527082 | |||||||
chr6:147527136 | A | G | 3 | a0001c0002t0004g0129 a0001c0002t0004g0130 a0003c0004t0016g0071 |
3 | HG02895.hp2 HG02897.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.459+17749A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527136 | |||||||
chr6:147527148 | C | T | 1 | a0001c0001t0017g0196 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.459+17761C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527148 | |||||||
chr6:147527225 | A | G | 37 | a0001c0001t0001g0184 a0001c0001t0001g0225 a0001c0001t0003g0060 others(34): Show |
37 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.459+17838A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527225 | |||||||
chr6:147527548 | G | A | 1 | a0001c0002t0008g0340 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.459+18161G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527548 | |||||||
chr6:147527575 | G | C | 19 | a0001c0001t0001g0005 a0001c0001t0027g0036 a0001c0001t0028g0253 others(16): Show |
20 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.459+18188G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527575 | |||||||
chr6:147527624 | A | G | 106 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0183 others(103): Show |
110 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.459+18237A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527624 | |||||||
chr6:147527631 | T | C | 295 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(292): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.459+18244T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527631 | |||||||
chr6:147527675 | C | A | 1 | a0001c0002t0004g0155 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.459+18288C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527675 | |||||||
chr6:147527804 | G | GT | 17 | a0001c0001t0011g0208 a0001c0001t0011g0209 a0001c0001t0011g0281 others(14): Show |
17 | HG01516.hp2 HG01517.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.459+18425dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147527804 | ||||||
chr6:147527847 | T | C | 1 | a0001c0001t0094g0210 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.459+18460T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527847 | |||||||
chr6:147527949 | G | C | 6 | a0001c0001t0027g0036 a0001c0001t0028g0297 a0001c0001t0081g0243 others(3): Show |
6 | HG02723.hp2 HG02818.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+18562G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527949 | |||||||
chr6:147527958 | A | G | 1 | a0001c0002t0004g0093 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.459+18571A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527958 | |||||||
chr6:147527985 | G | A | 12 | a0001c0001t0001g0009 a0001c0001t0001g0191 a0001c0001t0001g0198 others(9): Show |
13 | HG00280.hp1 HG00642.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.459+18598G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147527985 | |||||||
chr6:147528145 | A | G | 175 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0052 others(172): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.459+18758A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528145 | |||||||
chr6:147528227 | C | G | 107 | a0001c0001t0001g0038 a0001c0001t0001g0183 a0001c0001t0001g0256 others(104): Show |
110 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.459+18840C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528227 | |||||||
chr6:147528274 | C | T | 105 | a0001c0001t0001g0038 a0001c0001t0001g0183 a0001c0001t0001g0256 others(102): Show |
108 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.459+18887C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528274 | |||||||
chr6:147528357 | C | T | 1 | a0001c0002t0060g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.459+18970C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528357 | |||||||
chr6:147528373 | C | T | 30 | a0001c0001t0001g0256 a0001c0001t0003g0060 a0001c0001t0003g0299 others(27): Show |
30 | HG00609.hp2 HG02040.hp2 HG02071.hp2 others(27): Show |
intron_variant | MODIFIER | c.459+18986C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528373 | |||||||
chr6:147528479 | G | T | 2 | a0001c0002t0008g0342 a0005c0007t0011g0090 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.459+19092G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528479 | |||||||
chr6:147528573 | T | C | 1 | a0001c0001t0017g0007 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.459+19186T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528573 | |||||||
chr6:147528905 | T | C | 19 | a0001c0001t0001g0005 a0001c0001t0027g0036 a0001c0001t0028g0253 others(16): Show |
20 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.459+19518T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528905 | |||||||
chr6:147528937 | A | G | 1 | a0001c0001t0002g0334 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.459+19550A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147528937 | |||||||
chr6:147529014 | T | C | 21 | a0001c0001t0001g0005 a0001c0001t0027g0036 a0001c0001t0028g0253 others(18): Show |
22 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.459+19627T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529014 | |||||||
chr6:147529112 | A | G | 3 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0100g0227 |
3 | HG02132.hp2 NA18984.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.459+19725A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529112 | |||||||
chr6:147529145 | G | A | 1 | a0001c0002t0004g0100 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.459+19758G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529145 | |||||||
chr6:147529232 | T | G | 314 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(311): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.459+19845T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529232 | |||||||
chr6:147529293 | T | C | 1 | a0002c0003t0001g0021 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.459+19906T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529293 | |||||||
chr6:147529397 | C | T | 6 | a0001c0001t0003g0060 a0001c0001t0029g0144 a0001c0001t0085g0061 others(3): Show |
6 | HG01884.hp1 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+20010C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529397 | |||||||
chr6:147529416 | T | G | 2 | a0001c0001t0085g0061 a0001c0002t0022g0167 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.459+20029T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529416 | |||||||
chr6:147529461 | G | A | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.459+20074G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529461 | |||||||
chr6:147529500 | C | T | 1 | a0002c0003t0001g0032 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.459+20113C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529500 | |||||||
chr6:147529598 | G | T | 2 | a0001c0001t0001g0224 a0001c0002t0041g0128 |
2 | HG02129.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.459+20211G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529598 | |||||||
chr6:147529628 | A | C | 4 | a0001c0001t0027g0036 a0001c0001t0028g0297 a0001c0002t0008g0340 others(1): Show |
4 | HG02723.hp2 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.459+20241A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529628 | |||||||
chr6:147529650 | T | C | 1 | a0001c0002t0010g0177 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.459+20263T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529650 | |||||||
chr6:147529846 | G | A | 8 | a0001c0001t0003g0186 a0001c0001t0003g0228 a0001c0001t0003g0229 others(5): Show |
9 | NA18612.hp2 NA18939.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.459+20459G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529846 | |||||||
chr6:147529855 | A | G | 245 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0051 others(242): Show |
257 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.459+20468A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529855 | |||||||
chr6:147529949 | A | C | 2 | a0001c0002t0008g0342 a0005c0007t0011g0090 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.459+20562A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147529949 | |||||||
chr6:147530010 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.459+20623T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530010 | |||||||
chr6:147530085 | T | A | 1 | a0001c0001t0080g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.459+20698T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530085 | |||||||
chr6:147530087 | T | C | 14 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0337 others(11): Show |
15 | HG02132.hp2 HG02155.hp1 HG04204.hp2 others(12): Show |
intron_variant | MODIFIER | c.459+20700T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530087 | |||||||
chr6:147530155 | G | A | 266 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0051 others(263): Show |
278 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.459+20768G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530155 | |||||||
chr6:147530314 | C | T | 12 | a0001c0001t0001g0005 a0001c0001t0028g0253 a0001c0001t0106g0058 others(9): Show |
13 | HG01891.hp2 HG02451.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.459+20927C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530314 | |||||||
chr6:147530363 | C | T | 7 | a0001c0001t0001g0038 a0001c0001t0001g0183 a0001c0001t0011g0197 others(4): Show |
7 | HG01891.hp1 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+20976C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530363 | |||||||
chr6:147530399 | G | A | 2 | a0001c0001t0003g0011 a0001c0002t0010g0097 |
3 | NA18943.hp2 NA18964.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.459+21012G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530399 | |||||||
chr6:147530406 | C | G | 1 | a0001c0001t0003g0287 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.459+21019C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530406 | |||||||
chr6:147530442 | T | C | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.459+21055T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530442 | |||||||
chr6:147530494 | C | G | 3 | a0001c0001t0092g0217 a0001c0002t0004g0176 a0002c0003t0001g0021 |
3 | HG00280.hp2 HG00323.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.459+21107C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530494 | |||||||
chr6:147530599 | C | T | 2 | a0001c0002t0008g0342 a0005c0007t0011g0090 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.459+21212C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530599 | |||||||
chr6:147530679 | C | T | 11 | a0001c0001t0001g0005 a0001c0001t0106g0058 a0001c0002t0004g0129 others(8): Show |
12 | HG01891.hp2 HG02451.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.459+21292C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530679 | |||||||
chr6:147530838 | T | G | 75 | a0001c0001t0001g0038 a0001c0001t0001g0183 a0001c0001t0001g0266 others(72): Show |
78 | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.459+21451T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147530838 | |||||||
chr6:147531032 | C | A | 13 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0003g0186 others(10): Show |
14 | HG02132.hp2 HG04204.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.459+21645C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147531032 | |||||||
chr6:147531155 | GT | G | 7 | a0001c0001t0020g0192 a0001c0001t0102g0333 a0001c0001t0105g0194 others(4): Show |
7 | HG02109.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+21784delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147531155 | ||||||
chr6:147531155 | GTT | G | 62 | a0001c0001t0001g0005 a0001c0001t0001g0256 a0001c0001t0001g0291 others(59): Show |
64 | HG00423.hp1 HG00423.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.459+21783_459+2178 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147531155 | ||||||
chr6:147531155 | GTTT | G | 221 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0051 others(218): Show |
233 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.459+21782_459+2178 others(7): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147531155 | ||||||
chr6:147531162 | T | G | 2 | a0001c0001t0002g0269 a0001c0002t0007g0105 |
2 | HG01255.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.459+21775T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147531162 | |||||||
chr6:147531561 | G | A | 128 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0183 others(125): Show |
134 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(131): Show |
intron_variant | MODIFIER | c.459+22174G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147531561 | |||||||
chr6:147531841 | C | T | 2 | a0001c0001t0029g0144 a0003c0004t0020g0077 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.459+22454C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147531841 | |||||||
chr6:147531913 | A | G | 2 | a0001c0002t0004g0127 a0002c0003t0001g0032 |
2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.459+22526A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147531913 | |||||||
chr6:147532014 | T | A | 2 | a0001c0001t0005g0307 a0001c0001t0005g0308 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.459+22627T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532014 | |||||||
chr6:147532279 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.459+22892C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532279 | |||||||
chr6:147532281 | C | T | 6 | a0001c0001t0106g0058 a0001c0002t0042g0131 a0001c0002t0069g0107 others(3): Show |
6 | HG02922.hp2 HG02970.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.459+22894C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532281 | |||||||
chr6:147532303 | C | G | 5 | a0001c0001t0003g0060 a0001c0001t0029g0144 a0001c0002t0059g0079 others(2): Show |
5 | HG02965.hp2 HG03139.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+22916C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532303 | |||||||
chr6:147532329 | T | G | 3 | a0001c0001t0001g0005 a0001c0002t0004g0129 a0001c0002t0004g0130 |
4 | HG01891.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.459+22942T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532329 | |||||||
chr6:147532856 | G | A | 1 | a0001c0002t0010g0165 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.459+23469G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532856 | |||||||
chr6:147532951 | T | A | 1 | a0001c0001t0017g0007 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.459+23564T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532951 | |||||||
chr6:147532995 | A | G | 18 | a0001c0001t0001g0256 a0001c0001t0009g0039 a0001c0001t0009g0066 others(15): Show |
18 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.459+23608A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147532995 | |||||||
chr6:147533136 | A | G | 16 | a0001c0001t0012g0344 a0001c0001t0020g0152 a0001c0001t0020g0192 others(13): Show |
16 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.459+23749A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533136 | |||||||
chr6:147533165 | C | T | 1 | a0001c0001t0075g0233 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.459+23778C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533165 | |||||||
chr6:147533330 | C | T | 18 | a0001c0001t0001g0256 a0001c0001t0009g0039 a0001c0001t0009g0066 others(15): Show |
18 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.459+23943C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533330 | |||||||
chr6:147533447 | A | C | 1 | a0001c0002t0045g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.459+24060A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533447 | |||||||
chr6:147533462 | C | CA | 90 | a0001c0001t0001g0038 a0001c0001t0001g0183 a0001c0001t0001g0266 others(87): Show |
94 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.459+24093dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147533462 | ||||||
chr6:147533462 | CA | C | 72 | a0001c0001t0001g0256 a0001c0001t0003g0060 a0001c0001t0003g0064 others(69): Show |
73 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.459+24093delA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147533462 | ||||||
chr6:147533477 | A | G | 9 | a0001c0001t0012g0344 a0001c0001t0020g0152 a0001c0001t0020g0192 others(6): Show |
9 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.459+24090A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533477 | |||||||
chr6:147533553 | T | C | 1 | a0001c0001t0100g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.459+24166T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533553 | |||||||
chr6:147533587 | C | T | 3 | a0001c0001t0085g0061 a0001c0002t0022g0167 a0001c0002t0025g0341 |
3 | HG01884.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.459+24200C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533587 | |||||||
chr6:147533991 | C | G | 1 | a0001c0001t0001g0306 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.459+24604C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147533991 | |||||||
chr6:147534300 | C | T | 1 | a0001c0001t0006g0207 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.459+24913C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534300 | |||||||
chr6:147534350 | A | T | 191 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(188): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.459+24963A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534350 | |||||||
chr6:147534406 | C | G | 6 | a0001c0001t0001g0266 a0001c0001t0100g0227 a0001c0001t0102g0333 others(3): Show |
6 | HG02132.hp2 HG03209.hp1 HG03942.hp1 others(3): Show |
intron_variant | MODIFIER | c.459+25019C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534406 | |||||||
chr6:147534443 | G | A | 7 | a0001c0001t0012g0344 a0001c0001t0020g0152 a0001c0001t0020g0192 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.459+25056G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534443 | |||||||
chr6:147534487 | C | T | 5 | a0001c0001t0001g0266 a0001c0001t0100g0227 a0001c0001t0102g0333 others(2): Show |
5 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+25100C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534487 | |||||||
chr6:147534488 | A | G | 5 | a0001c0001t0001g0266 a0001c0001t0100g0227 a0001c0001t0102g0333 others(2): Show |
5 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+25101A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534488 | |||||||
chr6:147534512 | A | G | 5 | a0001c0001t0001g0266 a0001c0001t0100g0227 a0001c0001t0102g0333 others(2): Show |
5 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+25125A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534512 | |||||||
chr6:147534617 | T | C | 1 | a0001c0001t0017g0007 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.459+25230T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534617 | |||||||
chr6:147534712 | T | G | 5 | a0001c0001t0001g0266 a0001c0001t0100g0227 a0001c0001t0102g0333 others(2): Show |
5 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.459+25325T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534712 | |||||||
chr6:147534790 | G | C | 5 | a0001c0001t0002g0258 a0001c0001t0009g0053 a0001c0001t0009g0057 others(2): Show |
5 | HG00408.hp2 HG00423.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.459+25403G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147534790 | |||||||
chr6:147535235 | G | C | 313 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(310): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.459+25848G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535235 | |||||||
chr6:147535241 | G | A | 2 | a0001c0001t0011g0279 a0001c0001t0012g0033 |
2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.459+25854G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535241 | |||||||
chr6:147535375 | A | G | 17 | a0001c0001t0001g0256 a0001c0001t0009g0039 a0001c0001t0009g0066 others(14): Show |
17 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.459+25988A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535375 | |||||||
chr6:147535376 | A | T | 191 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(188): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.459+25989A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535376 | |||||||
chr6:147535409 | T | C | 13 | a0001c0001t0011g0197 a0001c0001t0011g0208 a0001c0001t0011g0209 others(10): Show |
13 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.459+26022T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535409 | |||||||
chr6:147535721 | C | T | 8 | a0001c0001t0095g0074 a0001c0001t0106g0058 a0001c0002t0008g0174 others(5): Show |
8 | HG02451.hp2 HG02922.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.459+26334C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535721 | |||||||
chr6:147535898 | C | T | 1 | a0001c0001t0005g0216 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.459+26511C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147535898 | |||||||
chr6:147536205 | A | G | 220 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(217): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.459+26818A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536205 | |||||||
chr6:147536263 | G | A | 2 | a0001c0002t0008g0150 a0001c0002t0008g0340 |
2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.459+26876G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536263 | |||||||
chr6:147536383 | G | A | 184 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(181): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.459+26996G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536383 | |||||||
chr6:147536474 | A | T | 222 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(219): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.459+27087A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536474 | |||||||
chr6:147536531 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.459+27144G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536531 | |||||||
chr6:147536560 | T | G | 1 | a0001c0002t0010g0177 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.459+27173T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536560 | |||||||
chr6:147536627 | C | G | 1 | a0001c0001t0102g0333 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.459+27240C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536627 | |||||||
chr6:147536826 | C | T | 21 | a0001c0001t0011g0197 a0001c0001t0011g0208 a0001c0001t0011g0209 others(18): Show |
21 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.459+27439C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536826 | |||||||
chr6:147536866 | A | G | 1 | a0004c0005t0029g0043 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.459+27479A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147536866 | |||||||
chr6:147537039 | A | C | 1 | a0001c0001t0104g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-27355A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537039 | |||||||
chr6:147537103 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.460-27291A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537103 | |||||||
chr6:147537107 | C | A | 5 | a0001c0001t0027g0036 a0001c0001t0085g0061 a0001c0002t0022g0086 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-27287C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537107 | |||||||
chr6:147537168 | A | T | 2 | a0001c0002t0004g0108 a0001c0002t0004g0109 |
2 | NA18995.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.460-27226A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537168 | |||||||
chr6:147537430 | C | A | 1 | a0001c0001t0009g0066 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.460-26964C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537430 | |||||||
chr6:147537567 | C | A | 8 | a0001c0001t0011g0279 a0001c0001t0012g0033 a0001c0001t0106g0058 others(5): Show |
8 | HG02572.hp1 HG02922.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.460-26827C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537567 | |||||||
chr6:147537567 | C | T | 12 | a0001c0001t0009g0039 a0001c0001t0009g0066 a0001c0001t0009g0200 others(9): Show |
12 | HG00609.hp2 HG02040.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.460-26827C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537567 | |||||||
chr6:147537584 | C | T | 185 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(182): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.460-26810C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537584 | |||||||
chr6:147537596 | C | CA | 183 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(180): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.460-26789dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147537596 | ||||||
chr6:147537630 | T | C | 1 | a0001c0002t0008g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.460-26764T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537630 | |||||||
chr6:147537636 | C | T | 13 | a0001c0001t0001g0266 a0001c0001t0011g0279 a0001c0001t0012g0033 others(10): Show |
13 | HG02132.hp2 HG02572.hp1 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.460-26758C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537636 | |||||||
chr6:147537645 | T | G | 1 | a0001c0002t0010g0163 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.460-26749T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537645 | |||||||
chr6:147537721 | C | A | 173 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(170): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.460-26673C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537721 | |||||||
chr6:147537755 | CA | C | 286 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(283): Show |
301 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.460-26625delA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147537755 | ||||||
chr6:147537755 | CAA | C | 24 | a0001c0001t0001g0306 a0001c0001t0009g0039 a0001c0001t0009g0066 others(21): Show |
24 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.460-26626_460-2662 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147537755 | ||||||
chr6:147537821 | A | G | 22 | a0001c0001t0011g0197 a0001c0001t0011g0208 a0001c0001t0011g0209 others(19): Show |
22 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.460-26573A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537821 | |||||||
chr6:147537872 | T | C | 6 | a0001c0001t0106g0058 a0001c0002t0042g0131 a0001c0002t0069g0107 others(3): Show |
6 | HG02922.hp2 HG02970.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-26522T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537872 | |||||||
chr6:147537962 | T | C | 2 | a0001c0001t0098g0187 a0001c0002t0056g0092 |
2 | HG02683.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.460-26432T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147537962 | |||||||
chr6:147538073 | T | G | 1 | a0001c0001t0001g0251 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.460-26321T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538073 | |||||||
chr6:147538192 | T | C | 1 | a0001c0002t0023g0088 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.460-26202T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538192 | |||||||
chr6:147538257 | T | A | 2 | a0001c0001t0009g0066 a0001c0001t0009g0200 |
2 | HG02040.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.460-26137T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538257 | |||||||
chr6:147538270 | G | T | 208 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(205): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.460-26124G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538270 | |||||||
chr6:147538349 | C | G | 22 | a0001c0001t0011g0197 a0001c0001t0011g0208 a0001c0001t0011g0209 others(19): Show |
22 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.460-26045C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538349 | |||||||
chr6:147538377 | C | T | 190 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(187): Show |
201 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.460-26017C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538377 | |||||||
chr6:147538462 | A | G | 22 | a0001c0001t0011g0197 a0001c0001t0011g0208 a0001c0001t0011g0209 others(19): Show |
22 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.460-25932A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538462 | |||||||
chr6:147538512 | T | G | 163 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(160): Show |
174 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.460-25882T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538512 | |||||||
chr6:147538988 | G | A | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-25406G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147538988 | |||||||
chr6:147539049 | G | A | 11 | a0001c0001t0012g0344 a0001c0001t0020g0152 a0001c0001t0020g0192 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.460-25345G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539049 | |||||||
chr6:147539057 | C | A | 8 | a0001c0001t0016g0226 a0001c0001t0028g0297 a0001c0001t0096g0054 others(5): Show |
8 | HG02145.hp2 HG02818.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-25337C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539057 | |||||||
chr6:147539077 | G | A | 11 | a0001c0001t0012g0344 a0001c0001t0020g0152 a0001c0001t0020g0192 others(8): Show |
11 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.460-25317G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539077 | |||||||
chr6:147539274 | C | CTAT | 199 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(196): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.460-25120_460-2511 others(7): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539274 | |||||||
chr6:147539329 | A | G | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.460-25065A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539329 | |||||||
chr6:147539549 | C | A | 10 | a0001c0001t0012g0010 a0001c0001t0012g0338 a0001c0001t0027g0245 others(7): Show |
11 | HG00738.hp1 HG01081.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.460-24845C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539549 | |||||||
chr6:147539658 | A | C | 7 | a0001c0001t0002g0050 a0001c0001t0002g0056 a0001c0001t0002g0223 others(4): Show |
7 | HG00597.hp1 HG02040.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-24736A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539658 | |||||||
chr6:147539702 | G | GA | 24 | a0001c0001t0009g0039 a0001c0001t0009g0066 a0001c0001t0009g0200 others(21): Show |
24 | HG00140.hp1 HG00609.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.460-24679dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147539702 | ||||||
chr6:147539821 | T | C | 1 | a0001c0002t0007g0096 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.460-24573T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539821 | |||||||
chr6:147539907 | C | T | 158 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(155): Show |
169 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.460-24487C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147539907 | |||||||
chr6:147540027 | A | G | 26 | a0001c0001t0001g0266 a0001c0001t0011g0197 a0001c0001t0011g0208 others(23): Show |
26 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.460-24367A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540027 | |||||||
chr6:147540077 | C | CT | 22 | a0001c0001t0011g0197 a0001c0001t0011g0208 a0001c0001t0011g0209 others(19): Show |
22 | HG01516.hp2 HG01517.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.460-24309dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540077 | ||||||
chr6:147540161 | G | A | 10 | a0001c0001t0012g0344 a0001c0001t0020g0152 a0001c0001t0020g0192 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-24233G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540161 | |||||||
chr6:147540175 | TA | T | 8 | a0001c0001t0012g0344 a0001c0001t0020g0152 a0001c0001t0020g0192 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-24218delA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540175 | |||||||
chr6:147540183 | A | T | 4 | a0001c0001t0001g0266 a0001c0001t0100g0227 a0001c0002t0004g0127 others(1): Show |
4 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-24211A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540183 | |||||||
chr6:147540223 | G | A | 10 | a0001c0001t0012g0344 a0001c0001t0020g0152 a0001c0001t0020g0192 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-24171G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540223 | |||||||
chr6:147540767 | C | CAG | 5 | a0001c0001t0001g0306 a0001c0001t0003g0202 a0001c0001t0086g0275 others(2): Show |
5 | HG02132.hp2 NA18966.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-23618_460-2361 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540767 | ||||||
chr6:147540777 | G | GA | 308 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(305): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.460-23617_460-2361 others(5): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540777 | |||||||
chr6:147540784 | G | T | 2 | a0001c0006t0015g0140 a0001c0006t0015g0141 |
2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.460-23610G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540784 | |||||||
chr6:147540843 | C | T | 1 | a0001c0002t0008g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.460-23551C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540843 | |||||||
chr6:147540903 | C | T | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-23491C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540903 | |||||||
chr6:147540931 | G | A | 7 | a0001c0001t0029g0144 a0001c0001t0106g0058 a0001c0002t0042g0131 others(4): Show |
7 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.460-23463G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540931 | |||||||
chr6:147540933 | G | GT | 66 | a0001c0001t0001g0183 a0001c0001t0001g0283 a0001c0001t0002g0006 others(63): Show |
70 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.460-23434dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540933 | ||||||
chr6:147540933 | G | GTT | 67 | a0001c0001t0001g0038 a0001c0001t0001g0293 a0001c0001t0001g0312 others(64): Show |
67 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.460-23435_460-2343 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540933 | ||||||
chr6:147540933 | GT | G | 85 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0184 others(82): Show |
88 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.460-23434delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540933 | ||||||
chr6:147540933 | GTT | G | 70 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0190 others(67): Show |
78 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.460-23435_460-2343 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540933 | ||||||
chr6:147540933 | GTTT | G | 9 | a0001c0001t0001g0256 a0001c0001t0020g0152 a0001c0001t0029g0144 others(6): Show |
9 | HG02055.hp2 HG02109.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.460-23436_460-2343 others(7): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540933 | ||||||
chr6:147540933 | GTTTT | G | 12 | a0001c0001t0012g0344 a0001c0001t0020g0192 a0001c0001t0096g0054 others(9): Show |
12 | HG00140.hp1 HG01975.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.460-23437_460-2343 others(8): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147540933 | ||||||
chr6:147540941 | T | A | 4 | a0001c0001t0001g0266 a0001c0001t0100g0227 a0001c0002t0004g0127 others(1): Show |
4 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-23453T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540941 | |||||||
chr6:147540941 | T | G | 3 | a0001c0001t0020g0152 a0001c0002t0036g0132 a0003c0004t0107g0069 |
3 | HG02055.hp2 HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.460-23453T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540941 | |||||||
chr6:147540942 | T | G | 15 | a0001c0001t0012g0344 a0001c0001t0020g0152 a0001c0001t0020g0192 others(12): Show |
15 | HG00140.hp1 HG01975.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-23452T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540942 | |||||||
chr6:147540943 | T | G | 12 | a0001c0001t0012g0344 a0001c0001t0020g0192 a0001c0001t0096g0054 others(9): Show |
12 | HG00140.hp1 HG01975.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.460-23451T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540943 | |||||||
chr6:147540944 | T | A | 4 | a0001c0001t0001g0266 a0001c0001t0100g0227 a0001c0002t0004g0127 others(1): Show |
4 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-23450T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540944 | |||||||
chr6:147540944 | T | TG | 2 | a0001c0001t0003g0011 a0001c0002t0010g0097 |
3 | NA18943.hp2 NA18964.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.460-23450_460-2344 others(5): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540944 | |||||||
chr6:147540945 | T | G | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-23449T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147540945 | |||||||
chr6:147541021 | C | T | 1 | a0001c0002t0004g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.460-23373C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541021 | |||||||
chr6:147541230 | G | A | 15 | a0001c0001t0012g0344 a0001c0001t0020g0152 a0001c0001t0020g0192 others(12): Show |
15 | HG00140.hp1 HG01975.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-23164G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541230 | |||||||
chr6:147541232 | A | G | 15 | a0001c0001t0012g0344 a0001c0001t0020g0152 a0001c0001t0020g0192 others(12): Show |
15 | HG00140.hp1 HG01975.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-23162A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541232 | |||||||
chr6:147541338 | G | T | 1 | a0001c0001t0104g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-23056G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541338 | |||||||
chr6:147541390 | C | T | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-23004C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541390 | |||||||
chr6:147541498 | C | T | 2 | a0001c0001t0005g0235 a0001c0002t0023g0088 |
2 | HG01169.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.460-22896C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541498 | |||||||
chr6:147541499 | G | A | 1 | a0001c0001t0005g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.460-22895G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541499 | |||||||
chr6:147541577 | G | A | 3 | a0001c0001t0001g0185 a0001c0001t0002g0304 a0001c0001t0002g0305 |
3 | HG00621.hp1 NA19007.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.460-22817G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541577 | |||||||
chr6:147541685 | T | C | 1 | a0001c0002t0008g0342 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.460-22709T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541685 | |||||||
chr6:147541687 | C | T | 1 | a0001c0002t0024g0162 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.460-22707C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541687 | |||||||
chr6:147541704 | G | A | 5 | a0001c0001t0002g0335 a0001c0001t0003g0231 a0001c0001t0003g0296 others(2): Show |
5 | NA18939.hp1 NA18963.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-22690G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541704 | |||||||
chr6:147541810 | T | C | 1 | a0001c0001t0002g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.460-22584T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541810 | |||||||
chr6:147541852 | T | A | 4 | a0001c0001t0001g0266 a0001c0001t0100g0227 a0001c0002t0004g0127 others(1): Show |
4 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-22542T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541852 | |||||||
chr6:147541968 | C | A | 2 | a0001c0001t0096g0054 a0001c0006t0053g0142 |
2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.460-22426C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541968 | |||||||
chr6:147541997 | G | A | 27 | a0001c0001t0001g0038 a0001c0001t0001g0183 a0001c0001t0009g0039 others(24): Show |
27 | HG00609.hp2 HG01081.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.460-22397G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147541997 | |||||||
chr6:147542079 | A | G | 1 | a0001c0001t0098g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.460-22315A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542079 | |||||||
chr6:147542109 | G | A | 3 | a0001c0001t0097g0065 a0001c0002t0010g0163 a0001c0002t0057g0169 |
3 | HG00140.hp1 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.460-22285G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542109 | |||||||
chr6:147542232 | A | C | 1 | a0001c0001t0006g0326 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.460-22162A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542232 | |||||||
chr6:147542257 | C | G | 1 | a0001c0001t0098g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.460-22137C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542257 | |||||||
chr6:147542315 | C | T | 2 | a0001c0001t0002g0319 a0001c0002t0007g0116 |
2 | HG00408.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.460-22079C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542315 | |||||||
chr6:147542317 | C | T | 2 | a0001c0001t0005g0322 a0001c0002t0013g0123 |
2 | NA18944.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.460-22077C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542317 | |||||||
chr6:147542362 | G | A | 127 | a0001c0001t0001g0225 a0001c0001t0001g0283 a0001c0001t0001g0293 others(124): Show |
132 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.460-22032G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542362 | |||||||
chr6:147542524 | G | A | 1 | a0001c0001t0100g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.460-21870G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542524 | |||||||
chr6:147542567 | A | T | 4 | a0001c0001t0011g0279 a0001c0001t0012g0033 a0001c0001t0095g0074 others(1): Show |
4 | HG02572.hp1 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-21827A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542567 | |||||||
chr6:147542599 | C | T | 34 | a0001c0001t0001g0225 a0001c0001t0002g0286 a0001c0001t0003g0064 others(31): Show |
34 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.460-21795C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542599 | |||||||
chr6:147542620 | G | A | 27 | a0001c0001t0001g0038 a0001c0001t0001g0183 a0001c0001t0009g0039 others(24): Show |
27 | HG00609.hp2 HG01081.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.460-21774G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542620 | |||||||
chr6:147542789 | C | T | 3 | a0001c0001t0011g0279 a0001c0001t0012g0033 a0001c0001t0113g0151 |
3 | HG02572.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.460-21605C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147542789 | |||||||
chr6:147543040 | TC | T | 6 | a0001c0001t0029g0144 a0001c0001t0106g0058 a0001c0002t0042g0131 others(3): Show |
6 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-21350delC | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147543040 | ||||||
chr6:147543071 | T | C | 1 | a0001c0001t0005g0238 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.460-21323T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543071 | |||||||
chr6:147543164 | A | C | 237 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(234): Show |
252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.460-21230A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543164 | |||||||
chr6:147543271 | C | G | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-21123C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543271 | |||||||
chr6:147543283 | G | A | 234 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(231): Show |
249 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.460-21111G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543283 | |||||||
chr6:147543358 | A | C | 2 | a0001c0001t0095g0074 a0001c0001t0103g0241 |
2 | HG02922.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.460-21036A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543358 | |||||||
chr6:147543526 | A | C | 238 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(235): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.460-20868A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543526 | |||||||
chr6:147543864 | T | G | 293 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(290): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.460-20530T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543864 | |||||||
chr6:147543911 | G | A | 6 | a0001c0001t0029g0144 a0001c0001t0106g0058 a0001c0002t0042g0131 others(3): Show |
6 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-20483G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147543911 | |||||||
chr6:147544061 | C | G | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-20333C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544061 | |||||||
chr6:147544063 | T | G | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-20331T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544063 | |||||||
chr6:147544106 | T | A | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-20288T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544106 | |||||||
chr6:147544387 | A | C | 3 | a0001c0001t0097g0065 a0001c0002t0010g0163 a0001c0002t0057g0169 |
3 | HG00140.hp1 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.460-20007A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544387 | |||||||
chr6:147544685 | G | A | 302 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(299): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.460-19709G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544685 | |||||||
chr6:147544694 | C | T | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-19700C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544694 | |||||||
chr6:147544778 | G | A | 2 | a0001c0002t0008g0110 a0001c0002t0008g0111 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.460-19616G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544778 | |||||||
chr6:147544807 | T | C | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-19587T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544807 | |||||||
chr6:147544840 | T | C | 1 | a0001c0002t0014g0102 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.460-19554T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147544840 | |||||||
chr6:147545076 | G | C | 9 | a0001c0001t0011g0279 a0001c0001t0012g0033 a0001c0001t0029g0144 others(6): Show |
9 | HG02572.hp1 HG02922.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-19318G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545076 | |||||||
chr6:147545088 | C | T | 34 | a0001c0001t0001g0038 a0001c0001t0001g0183 a0001c0001t0009g0039 others(31): Show |
34 | HG00609.hp2 HG01081.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.460-19306C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545088 | |||||||
chr6:147545299 | C | T | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-19095C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545299 | |||||||
chr6:147545480 | T | C | 306 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(303): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.460-18914T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545480 | |||||||
chr6:147545562 | G | T | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.460-18832G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545562 | |||||||
chr6:147545566 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.460-18828C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545566 | |||||||
chr6:147545690 | A | T | 3 | a0001c0002t0008g0150 a0001c0002t0008g0181 a0001c0002t0008g0340 |
3 | HG02818.hp1 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.460-18704A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147545690 | |||||||
chr6:147546017 | T | C | 2 | a0001c0001t0001g0242 a0001c0001t0079g0268 |
2 | NA19010.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.460-18377T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546017 | |||||||
chr6:147546259 | G | T | 2 | a0001c0001t0003g0060 a0001c0001t0028g0253 |
2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.460-18135G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546259 | |||||||
chr6:147546306 | G | T | 1 | a0001c0001t0001g0306 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.460-18088G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546306 | |||||||
chr6:147546356 | C | T | 3 | a0001c0002t0004g0089 a0001c0002t0068g0067 a0003c0004t0016g0072 |
3 | HG01891.hp1 HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.460-18038C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546356 | |||||||
chr6:147546393 | G | C | 1 | a0001c0001t0100g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.460-18001G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546393 | |||||||
chr6:147546399 | G | A | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-17995G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546399 | |||||||
chr6:147546406 | T | G | 1 | a0001c0001t0086g0275 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.460-17988T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546406 | |||||||
chr6:147546466 | T | G | 307 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(304): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.460-17928T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546466 | |||||||
chr6:147546471 | G | A | 2 | a0001c0001t0020g0192 a0001c0002t0026g0087 |
2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.460-17923G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546471 | |||||||
chr6:147546530 | C | CAAAAAAA | 22 | a0001c0001t0001g0038 a0001c0001t0001g0183 a0001c0001t0012g0264 others(19): Show |
22 | HG01109.hp2 HG01891.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.460-17857_460-1785 others(11): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147546530 | ||||||
chr6:147546530 | C | CAAAAAAA others(1): Show |
15 | a0001c0001t0001g0185 a0001c0001t0009g0057 a0001c0001t0009g0066 others(12): Show |
15 | HG01081.hp1 HG02040.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.460-17858_460-1785 others(12): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147546530 | ||||||
chr6:147546530 | C | CAAAAAAA others(2): Show |
24 | a0001c0001t0001g0266 a0001c0001t0003g0284 a0001c0001t0005g0313 others(21): Show |
24 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.460-17859_460-1785 others(13): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147546530 | ||||||
chr6:147546530 | C | CAAAAAAA others(3): Show |
230 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(227): Show |
244 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.460-17860_460-1785 others(14): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147546530 | ||||||
chr6:147546530 | C | CAAAAAAA others(4): Show |
12 | a0001c0001t0001g0302 a0001c0001t0002g0290 a0001c0001t0005g0317 others(9): Show |
13 | HG00140.hp1 HG01975.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.460-17861_460-1785 others(15): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147546530 | ||||||
chr6:147546541 | A | AAAAAAAA others(3): Show |
2 | a0001c0001t0001g0312 a0001c0002t0007g0122 |
2 | HG02027.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.460-17851_460-1785 others(14): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147546541 | ||||||
chr6:147546574 | T | C | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-17820T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546574 | |||||||
chr6:147546635 | C | G | 302 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(299): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.460-17759C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546635 | |||||||
chr6:147546684 | C | A | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-17710C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546684 | |||||||
chr6:147546698 | T | C | 1 | a0001c0001t0091g0034 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.460-17696T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147546698 | |||||||
chr6:147547478 | A | G | 6 | a0001c0001t0029g0144 a0001c0001t0106g0058 a0001c0002t0042g0131 others(3): Show |
6 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-16916A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547478 | |||||||
chr6:147547520 | C | T | 244 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(241): Show |
259 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.460-16874C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547520 | |||||||
chr6:147547553 | G | C | 6 | a0001c0001t0029g0144 a0001c0001t0106g0058 a0001c0002t0042g0131 others(3): Show |
6 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-16841G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547553 | |||||||
chr6:147547586 | T | C | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-16808T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547586 | |||||||
chr6:147547649 | C | T | 8 | a0001c0001t0002g0035 a0001c0001t0002g0230 a0001c0001t0002g0289 others(5): Show |
8 | HG01255.hp2 HG02155.hp1 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.460-16745C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547649 | |||||||
chr6:147547674 | T | C | 5 | a0001c0001t0001g0266 a0001c0001t0100g0227 a0001c0001t0102g0333 others(2): Show |
5 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.460-16720T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547674 | |||||||
chr6:147547698 | C | A | 3 | a0001c0001t0005g0218 a0001c0001t0005g0276 a0001c0002t0054g0154 |
3 | HG00733.hp2 HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.460-16696C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547698 | |||||||
chr6:147547998 | A | G | 1 | a0003c0004t0110g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.460-16396A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147547998 | |||||||
chr6:147548043 | T | G | 248 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(245): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.460-16351T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147548043 | |||||||
chr6:147548101 | A | G | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-16293A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147548101 | |||||||
chr6:147548112 | TATA | T | 38 | a0001c0001t0001g0038 a0001c0001t0001g0183 a0001c0001t0001g0185 others(35): Show |
38 | HG00609.hp2 HG01081.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.460-16275_460-1627 others(7): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147548112 | ||||||
chr6:147548147 | G | A | 263 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(260): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.460-16247G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147548147 | |||||||
chr6:147548655 | T | C | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-15739T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147548655 | |||||||
chr6:147548922 | A | G | 3 | a0001c0001t0011g0279 a0001c0001t0012g0033 a0001c0001t0113g0151 |
3 | HG02572.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.460-15472A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147548922 | |||||||
chr6:147549095 | T | C | 1 | a0001c0002t0065g0135 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.460-15299T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549095 | |||||||
chr6:147549115 | A | C | 251 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(248): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.460-15279A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549115 | |||||||
chr6:147549264 | G | C | 1 | a0001c0001t0089g0044 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.460-15130G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549264 | |||||||
chr6:147549370 | G | A | 38 | a0001c0001t0001g0038 a0001c0001t0001g0183 a0001c0001t0001g0185 others(35): Show |
38 | HG00609.hp2 HG01081.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.460-15024G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549370 | |||||||
chr6:147549558 | T | C | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-14836T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549558 | |||||||
chr6:147549859 | C | T | 1 | a0001c0001t0005g0252 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.460-14535C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549859 | |||||||
chr6:147549889 | G | C | 236 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(233): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.460-14505G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549889 | |||||||
chr6:147549937 | C | T | 2 | a0001c0001t0096g0054 a0001c0006t0053g0142 |
2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.460-14457C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147549937 | |||||||
chr6:147550101 | T | C | 251 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(248): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.460-14293T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550101 | |||||||
chr6:147550234 | G | A | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-14160G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550234 | |||||||
chr6:147550398 | A | G | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-13996A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550398 | |||||||
chr6:147550528 | T | C | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-13866T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550528 | |||||||
chr6:147550548 | T | C | 1 | a0001c0001t0100g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.460-13846T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550548 | |||||||
chr6:147550709 | C | CA | 306 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(303): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.460-13683dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147550709 | ||||||
chr6:147550768 | A | T | 251 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(248): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.460-13626A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550768 | |||||||
chr6:147550868 | G | A | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-13526G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550868 | |||||||
chr6:147550900 | T | TTA | 250 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(247): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.460-13481_460-1348 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147550900 | ||||||
chr6:147550991 | T | C | 4 | a0001c0001t0001g0266 a0001c0001t0100g0227 a0001c0002t0004g0127 others(1): Show |
4 | HG02132.hp2 HG03942.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-13403T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147550991 | |||||||
chr6:147551012 | G | A | 244 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(241): Show |
259 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.460-13382G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551012 | |||||||
chr6:147551045 | G | A | 246 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0051 others(243): Show |
261 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.460-13349G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551045 | |||||||
chr6:147551080 | A | G | 175 | a0001c0001t0001g0005 a0001c0001t0001g0225 a0001c0001t0001g0283 others(172): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.460-13314A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551080 | |||||||
chr6:147551138 | A | G | 3 | a0001c0001t0097g0065 a0001c0002t0010g0163 a0001c0002t0057g0169 |
3 | HG00140.hp1 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.460-13256A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551138 | |||||||
chr6:147551151 | G | C | 7 | a0001c0001t0029g0144 a0001c0001t0104g0244 a0001c0001t0106g0058 others(4): Show |
7 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.460-13243G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551151 | |||||||
chr6:147551158 | G | A | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-13236G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551158 | |||||||
chr6:147551174 | A | G | 327 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(324): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.460-13220A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551174 | |||||||
chr6:147551176 | T | G | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-13218T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551176 | |||||||
chr6:147551350 | C | A | 187 | a0001c0001t0001g0225 a0001c0001t0001g0266 a0001c0001t0001g0293 others(184): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.460-13044C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551350 | |||||||
chr6:147551485 | AC | A | 3 | a0001c0001t0106g0058 a0001c0002t0023g0082 a0003c0004t0110g0070 |
3 | HG02559.hp1 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.460-12907delC | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551485 | ||||||
chr6:147551643 | G | A | 305 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(302): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.460-12751G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551643 | |||||||
chr6:147551734 | T | A | 2 | a0001c0001t0005g0322 a0001c0002t0013g0123 |
2 | NA18944.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.460-12660T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551734 | |||||||
chr6:147551747 | G | A | 6 | a0001c0001t0029g0144 a0001c0001t0106g0058 a0001c0002t0042g0131 others(3): Show |
6 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-12647G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551747 | |||||||
chr6:147551812 | T | TTATA | 10 | a0001c0001t0001g0038 a0001c0001t0001g0185 a0001c0001t0001g0283 others(7): Show |
11 | HG00558.hp1 HG02683.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.460-12560_460-1255 others(8): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | T | TTATATA | 16 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0302 others(13): Show |
17 | HG01192.hp1 HG01261.hp1 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.460-12562_460-1255 others(10): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | T | TTATATAT others(1): Show |
47 | a0001c0001t0001g0009 a0001c0001t0001g0184 a0001c0001t0001g0190 others(44): Show |
50 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.460-12564_460-1255 others(12): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | T | TTATATAT others(3): Show |
22 | a0001c0001t0001g0005 a0001c0001t0001g0051 a0001c0001t0001g0052 others(19): Show |
23 | HG01891.hp2 HG02040.hp1 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.460-12566_460-1255 others(14): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | T | TTATATAT others(5): Show |
10 | a0001c0001t0001g0266 a0001c0001t0002g0056 a0001c0001t0002g0265 others(7): Show |
10 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-12568_460-1255 others(16): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | T | TTATATAT others(7): Show |
5 | a0001c0001t0001g0291 a0001c0002t0004g0084 a0001c0002t0004g0171 others(2): Show |
5 | HG00423.hp2 HG01071.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-12570_460-1255 others(18): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | T | TTATATAT others(9): Show |
4 | a0001c0001t0009g0273 a0001c0002t0023g0082 a0003c0004t0110g0070 others(1): Show |
4 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-12572_460-1255 others(20): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | T | TTATATAT others(11): Show |
4 | a0001c0001t0106g0058 a0001c0002t0004g0083 a0001c0002t0042g0131 others(1): Show |
4 | HG01081.hp1 HG01109.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-12574_460-1255 others(22): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | T | TTATATAT others(13): Show |
1 | a0001c0001t0029g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.460-12576_460-1255 others(24): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | T | TTATATAT others(15): Show |
1 | a0001c0002t0069g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.460-12578_460-1255 others(26): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | T | TTATATAT others(19): Show |
1 | a0001c0002t0004g0073 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.460-12557_460-1255 others(30): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | TTA | T | 6 | a0001c0001t0005g0214 a0001c0001t0016g0226 a0001c0002t0061g0125 others(3): Show |
6 | HG01243.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-12558_460-1255 others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | TTATA | T | 10 | a0001c0001t0020g0152 a0001c0001t0020g0192 a0001c0001t0104g0244 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.460-12560_460-1255 others(8): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | TTATATA | T | 11 | a0001c0001t0002g0223 a0001c0001t0027g0036 a0001c0001t0085g0061 others(8): Show |
11 | HG01884.hp1 HG02056.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.460-12562_460-1255 others(10): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551812 | TTATATAT others(1): Show |
T | 167 | a0001c0001t0001g0225 a0001c0001t0001g0293 a0001c0001t0001g0312 others(164): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.460-12564_460-1255 others(12): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551812 | ||||||
chr6:147551816 | A | T | 4 | a0001c0001t0016g0226 a0003c0004t0016g0071 a0004c0005t0034g0046 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.460-12578A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551816 | |||||||
chr6:147551820 | A | ATATATAT others(65): Show |
1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-12561_460-1256 others(76): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551820 | ||||||
chr6:147551820 | A | T | 7 | a0001c0001t0002g0223 a0001c0001t0027g0036 a0001c0001t0085g0061 others(4): Show |
7 | HG01884.hp1 HG02056.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-12574A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551820 | |||||||
chr6:147551822 | A | T | 167 | a0001c0001t0001g0225 a0001c0001t0001g0293 a0001c0001t0001g0312 others(164): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.460-12572A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551822 | |||||||
chr6:147551897 | C | CCAAATT | 173 | a0001c0001t0001g0225 a0001c0001t0001g0293 a0001c0001t0001g0312 others(170): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.460-12495_460-1249 others(10): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147551897 | ||||||
chr6:147551901 | T | C | 1 | a0001c0002t0066g0094 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.460-12493T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551901 | |||||||
chr6:147551955 | G | A | 176 | a0001c0001t0001g0225 a0001c0001t0001g0293 a0001c0001t0001g0312 others(173): Show |
185 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.460-12439G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551955 | |||||||
chr6:147551976 | G | C | 181 | a0001c0001t0001g0225 a0001c0001t0001g0293 a0001c0001t0001g0312 others(178): Show |
190 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.460-12418G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147551976 | |||||||
chr6:147552042 | C | T | 1 | a0001c0001t0011g0197 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.460-12352C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147552042 | |||||||
chr6:147552144 | T | C | 1 | a0001c0002t0022g0167 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.460-12250T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147552144 | |||||||
chr6:147552803 | T | C | 1 | a0001c0001t0002g0334 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.460-11591T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147552803 | |||||||
chr6:147552976 | T | A | 5 | a0001c0001t0029g0144 a0001c0001t0106g0058 a0001c0002t0042g0131 others(2): Show |
5 | HG02922.hp2 HG02970.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-11418T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147552976 | |||||||
chr6:147553000 | G | A | 2 | a0001c0001t0100g0227 a0001c0001t0103g0241 |
2 | HG02132.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.460-11394G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553000 | |||||||
chr6:147553245 | C | G | 166 | a0001c0001t0001g0225 a0001c0001t0001g0312 a0001c0001t0001g0339 others(163): Show |
174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.460-11149C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553245 | |||||||
chr6:147553251 | C | G | 21 | a0001c0001t0016g0226 a0001c0001t0020g0152 a0001c0001t0020g0192 others(18): Show |
21 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.460-11143C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553251 | |||||||
chr6:147553743 | C | T | 7 | a0001c0001t0001g0224 a0001c0001t0001g0242 a0001c0001t0001g0247 others(4): Show |
7 | HG00597.hp2 HG02129.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-10651C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553743 | |||||||
chr6:147553803 | A | G | 102 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0052 others(99): Show |
107 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.460-10591A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553803 | |||||||
chr6:147553986 | T | C | 1 | a0001c0002t0069g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.460-10408T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553986 | |||||||
chr6:147553987 | A | G | 2 | a0001c0001t0027g0036 a0001c0002t0022g0086 |
2 | HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.460-10407A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147553987 | |||||||
chr6:147554001 | G | A | 8 | a0001c0001t0002g0050 a0001c0001t0002g0056 a0001c0001t0002g0203 others(5): Show |
8 | HG00597.hp1 HG02040.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.460-10393G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554001 | |||||||
chr6:147554162 | C | T | 1 | a0001c0002t0004g0119 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.460-10232C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554162 | |||||||
chr6:147554214 | C | T | 2 | a0001c0001t0081g0243 a0003c0004t0110g0070 |
2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.460-10180C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554214 | |||||||
chr6:147554329 | A | G | 1 | a0001c0001t0095g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.460-10065A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554329 | |||||||
chr6:147554361 | C | T | 2 | a0001c0001t0081g0243 a0003c0004t0110g0070 |
2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.460-10033C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554361 | |||||||
chr6:147554377 | G | A | 14 | a0001c0001t0001g0185 a0001c0001t0001g0283 a0001c0001t0009g0039 others(11): Show |
14 | HG00558.hp1 HG00609.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.460-10017G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554377 | |||||||
chr6:147554477 | A | G | 1 | a0001c0001t0086g0275 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.460-9917A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554477 | |||||||
chr6:147554483 | C | G | 2 | a0001c0001t0081g0243 a0003c0004t0110g0070 |
2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.460-9911C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554483 | |||||||
chr6:147554588 | GT | G | 10 | a0001c0001t0020g0152 a0001c0001t0020g0192 a0001c0001t0105g0194 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.460-9800delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147554588 | ||||||
chr6:147554595 | C | G | 10 | a0001c0001t0020g0152 a0001c0001t0020g0192 a0001c0001t0105g0194 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.460-9799C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554595 | |||||||
chr6:147554621 | C | T | 1 | a0001c0002t0060g0124 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.460-9773C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554621 | |||||||
chr6:147554662 | G | T | 10 | a0001c0001t0002g0258 a0001c0001t0002g0304 a0001c0001t0002g0305 others(7): Show |
11 | HG00621.hp1 HG01928.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.460-9732G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554662 | |||||||
chr6:147554731 | C | T | 6 | a0001c0001t0002g0232 a0001c0001t0002g0334 a0001c0002t0008g0179 others(3): Show |
6 | HG00558.hp2 HG00609.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.460-9663C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554731 | |||||||
chr6:147554798 | C | T | 1 | a0001c0002t0007g0122 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.460-9596C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554798 | |||||||
chr6:147554875 | C | T | 202 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0183 others(199): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.460-9519C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554875 | |||||||
chr6:147554887 | C | T | 1 | a0003c0004t0020g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.460-9507C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554887 | |||||||
chr6:147554902 | T | C | 170 | a0001c0001t0001g0225 a0001c0001t0001g0312 a0001c0001t0001g0339 others(167): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.460-9492T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147554902 | |||||||
chr6:147555028 | A | G | 2 | a0001c0001t0100g0227 a0001c0001t0103g0241 |
2 | HG02132.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.460-9366A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555028 | |||||||
chr6:147555124 | T | G | 7 | a0001c0001t0027g0036 a0001c0001t0027g0245 a0001c0001t0081g0243 others(4): Show |
7 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-9270T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555124 | |||||||
chr6:147555245 | C | A | 31 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0183 others(28): Show |
32 | HG00558.hp1 HG00609.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.460-9149C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555245 | |||||||
chr6:147555333 | A | G | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-9061A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555333 | |||||||
chr6:147555334 | C | G | 1 | a0001c0001t0001g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.460-9060C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555334 | |||||||
chr6:147555500 | T | C | 1 | a0001c0001t0079g0268 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.460-8894T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555500 | |||||||
chr6:147555511 | C | T | 1 | a0001c0002t0056g0092 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.460-8883C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555511 | |||||||
chr6:147555552 | G | A | 4 | a0001c0001t0009g0039 a0001c0001t0009g0271 a0001c0001t0009g0272 others(1): Show |
4 | HG00609.hp2 HG02074.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-8842G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555552 | |||||||
chr6:147555705 | T | C | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-8689T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555705 | |||||||
chr6:147555850 | A | G | 3 | a0001c0001t0003g0011 a0001c0001t0003g0285 a0001c0002t0010g0097 |
4 | NA18943.hp2 NA18964.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-8544A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555850 | |||||||
chr6:147555891 | T | C | 7 | a0001c0001t0027g0036 a0001c0001t0027g0245 a0001c0001t0081g0243 others(4): Show |
7 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-8503T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147555891 | |||||||
chr6:147556097 | A | AT | 6 | a0001c0001t0016g0226 a0001c0002t0068g0067 a0003c0004t0016g0071 others(3): Show |
6 | HG01891.hp1 HG02615.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-8284dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147556097 | ||||||
chr6:147556100 | T | A | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-8294T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556100 | |||||||
chr6:147556121 | C | T | 1 | a0001c0002t0007g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.460-8273C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556121 | |||||||
chr6:147556131 | C | T | 32 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0183 others(29): Show |
33 | HG00558.hp1 HG00609.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.460-8263C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556131 | |||||||
chr6:147556132 | G | A | 1 | a0001c0002t0024g0112 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.460-8262G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556132 | |||||||
chr6:147556218 | G | T | 1 | a0001c0001t0001g0183 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.460-8176G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556218 | |||||||
chr6:147556237 | C | T | 3 | a0001c0002t0008g0150 a0001c0002t0008g0181 a0001c0002t0008g0340 |
3 | HG02818.hp1 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.460-8157C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556237 | |||||||
chr6:147556313 | C | T | 6 | a0001c0001t0027g0036 a0001c0001t0027g0245 a0001c0001t0085g0061 others(3): Show |
6 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-8081C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556313 | |||||||
chr6:147556401 | A | C | 6 | a0001c0001t0027g0036 a0001c0001t0027g0245 a0001c0001t0085g0061 others(3): Show |
6 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-7993A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556401 | |||||||
chr6:147556559 | C | T | 2 | a0001c0001t0005g0214 a0001c0002t0038g0149 |
2 | HG01243.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.460-7835C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556559 | |||||||
chr6:147556778 | A | G | 2 | a0001c0001t0113g0151 a0003c0004t0107g0069 |
2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.460-7616A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556778 | |||||||
chr6:147556837 | C | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0038 a0001c0001t0001g0183 others(27): Show |
31 | HG00558.hp1 HG00609.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.460-7557C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556837 | |||||||
chr6:147556861 | A | G | 1 | a0002c0003t0001g0031 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.460-7533A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556861 | |||||||
chr6:147556908 | A | G | 7 | a0001c0001t0020g0152 a0001c0001t0020g0192 a0001c0001t0105g0194 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.460-7486A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556908 | |||||||
chr6:147556950 | G | A | 1 | a0001c0001t0005g0235 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.460-7444G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147556950 | |||||||
chr6:147557080 | T | A | 12 | a0001c0001t0001g0339 a0001c0001t0011g0279 a0001c0001t0028g0297 others(9): Show |
12 | HG01192.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.460-7314T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557080 | |||||||
chr6:147557277 | C | T | 27 | a0001c0001t0001g0339 a0001c0001t0011g0208 a0001c0001t0011g0209 others(24): Show |
27 | HG00140.hp1 HG00733.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.460-7117C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557277 | |||||||
chr6:147557280 | T | C | 74 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0052 others(71): Show |
79 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.460-7114T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557280 | |||||||
chr6:147557362 | T | C | 1 | a0001c0002t0036g0132 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.460-7032T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557362 | |||||||
chr6:147557515 | G | A | 1 | a0001c0001t0100g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.460-6879G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557515 | |||||||
chr6:147557654 | T | C | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-6740T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557654 | |||||||
chr6:147557826 | G | A | 2 | a0001c0001t0009g0066 a0001c0001t0009g0200 |
2 | HG02040.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.460-6568G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557826 | |||||||
chr6:147557952 | C | A | 7 | a0001c0001t0027g0036 a0001c0001t0027g0245 a0001c0001t0081g0243 others(4): Show |
7 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-6442C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147557952 | |||||||
chr6:147558043 | G | A | 1 | a0001c0001t0003g0202 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.460-6351G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558043 | |||||||
chr6:147558134 | A | C | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-6260A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558134 | |||||||
chr6:147558302 | G | A | 6 | a0001c0001t0027g0036 a0001c0001t0027g0245 a0001c0001t0085g0061 others(3): Show |
6 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-6092G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558302 | |||||||
chr6:147558334 | G | A | 1 | a0001c0001t0006g0328 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.460-6060G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558334 | |||||||
chr6:147558573 | C | T | 76 | a0001c0001t0001g0009 a0001c0001t0001g0051 a0001c0001t0001g0052 others(73): Show |
81 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.460-5821C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558573 | |||||||
chr6:147558704 | C | T | 1 | a0001c0001t0027g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.460-5690C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558704 | |||||||
chr6:147558899 | C | T | 8 | a0001c0001t0081g0243 a0001c0001t0095g0074 a0001c0001t0096g0054 others(5): Show |
8 | HG02132.hp2 HG02145.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.460-5495C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558899 | |||||||
chr6:147558903 | A | T | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-5491A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558903 | |||||||
chr6:147558939 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0248 |
2 | HG00642.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.460-5455G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147558939 | |||||||
chr6:147559084 | A | G | 14 | a0001c0001t0027g0036 a0001c0001t0027g0245 a0001c0001t0081g0243 others(11): Show |
14 | HG01884.hp1 HG02132.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.460-5310A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147559084 | |||||||
chr6:147559528 | G | A | 2 | a0001c0001t0001g0225 a0001c0002t0004g0161 |
2 | HG00642.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.460-4866G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147559528 | |||||||
chr6:147559627 | C | A | 2 | a0001c0001t0081g0243 a0001c0002t0023g0088 |
2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.460-4767C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147559627 | |||||||
chr6:147559690 | C | G | 29 | a0001c0001t0001g0339 a0001c0001t0011g0197 a0001c0001t0011g0208 others(26): Show |
29 | HG00140.hp1 HG00733.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-4704C>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147559690 | |||||||
chr6:147559716 | T | C | 12 | a0001c0001t0011g0208 a0001c0001t0011g0209 a0001c0001t0011g0221 others(9): Show |
12 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.460-4678T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147559716 | |||||||
chr6:147559865 | A | C | 212 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(209): Show |
220 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.460-4529A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147559865 | |||||||
chr6:147560035 | A | G | 180 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(177): Show |
188 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.460-4359A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560035 | |||||||
chr6:147560181 | T | G | 1 | a0001c0001t0103g0241 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.460-4213T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560181 | |||||||
chr6:147560223 | T | C | 1 | a0001c0001t0081g0243 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.460-4171T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560223 | |||||||
chr6:147560227 | A | G | 1 | a0001c0001t0078g0321 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.460-4167A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560227 | |||||||
chr6:147560239 | T | C | 2 | a0001c0001t0003g0060 a0001c0001t0028g0253 |
2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.460-4155T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560239 | |||||||
chr6:147560380 | G | T | 2 | a0001c0001t0001g0324 a0001c0002t0047g0118 |
2 | NA18980.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.460-4014G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560380 | |||||||
chr6:147560456 | A | G | 7 | a0001c0001t0027g0036 a0001c0001t0027g0245 a0001c0001t0028g0297 others(4): Show |
7 | HG01884.hp1 HG02723.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.460-3938A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560456 | |||||||
chr6:147560586 | A | T | 3 | a0001c0001t0003g0042 a0001c0001t0003g0284 a0001c0001t0003g0287 |
3 | NA18944.hp2 NA18975.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.460-3808A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560586 | |||||||
chr6:147560618 | C | A | 1 | a0001c0002t0004g0161 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.460-3776C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560618 | |||||||
chr6:147560702 | A | T | 1 | a0003c0004t0110g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.460-3692A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560702 | |||||||
chr6:147560743 | G | A | 1 | a0002c0003t0002g0017 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.460-3651G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560743 | |||||||
chr6:147560825 | A | G | 1 | a0001c0002t0036g0132 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.460-3569A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560825 | |||||||
chr6:147560885 | A | G | 2 | a0001c0001t0003g0186 a0001c0001t0003g0229 |
2 | NA18939.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.460-3509A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560885 | |||||||
chr6:147560947 | C | T | 9 | a0001c0001t0016g0226 a0001c0001t0016g0246 a0001c0001t0112g0254 others(6): Show |
9 | HG00140.hp2 HG00733.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.460-3447C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147560947 | |||||||
chr6:147561046 | G | T | 1 | a0001c0001t0002g0334 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.460-3348G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561046 | |||||||
chr6:147561186 | A | AATTT | 4 | a0001c0001t0100g0227 a0001c0001t0101g0277 a0001c0001t0102g0333 others(1): Show |
4 | HG02132.hp2 HG03491.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-3187_460-3184d others(6): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147561186 | ||||||
chr6:147561216 | C | T | 4 | a0001c0001t0100g0227 a0001c0001t0101g0277 a0001c0001t0102g0333 others(1): Show |
4 | HG02132.hp2 HG03491.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-3178C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561216 | |||||||
chr6:147561256 | C | T | 4 | a0001c0001t0100g0227 a0001c0001t0101g0277 a0001c0001t0102g0333 others(1): Show |
4 | HG02132.hp2 HG03491.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-3138C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561256 | |||||||
chr6:147561273 | C | T | 4 | a0001c0001t0100g0227 a0001c0001t0101g0277 a0001c0001t0102g0333 others(1): Show |
4 | HG02132.hp2 HG03491.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.460-3121C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561273 | |||||||
chr6:147561362 | A | G | 3 | a0001c0001t0108g0059 a0001c0002t0061g0125 a0003c0004t0110g0070 |
3 | HG02809.hp1 HG03195.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.460-3032A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561362 | |||||||
chr6:147561507 | A | C | 30 | a0001c0001t0001g0339 a0001c0001t0011g0197 a0001c0001t0011g0208 others(27): Show |
30 | HG00140.hp1 HG00733.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.460-2887A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561507 | |||||||
chr6:147561709 | T | G | 303 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(300): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.460-2685T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561709 | |||||||
chr6:147561747 | A | T | 1 | a0001c0001t0001g0339 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.460-2647A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561747 | |||||||
chr6:147561872 | C | T | 1 | a0001c0002t0051g0104 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.460-2522C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147561872 | |||||||
chr6:147562000 | G | A | 29 | a0001c0001t0001g0339 a0001c0001t0011g0208 a0001c0001t0011g0209 others(26): Show |
29 | HG00140.hp1 HG00733.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.460-2394G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562000 | |||||||
chr6:147562160 | T | G | 1 | a0001c0001t0003g0202 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.460-2234T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562160 | |||||||
chr6:147562273 | G | C | 1 | a0001c0001t0001g0266 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.460-2121G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562273 | |||||||
chr6:147562298 | A | G | 3 | a0001c0001t0002g0258 a0001c0002t0007g0099 a0001c0002t0007g0147 |
3 | HG02027.hp2 NA18948.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.460-2096A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562298 | |||||||
chr6:147562323 | T | C | 2 | a0001c0001t0005g0307 a0001c0001t0005g0308 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.460-2071T>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562323 | |||||||
chr6:147562324 | G | C | 1 | a0001c0001t0003g0202 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.460-2070G>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562324 | |||||||
chr6:147562652 | C | T | 1 | a0003c0004t0110g0070 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.460-1742C>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562652 | |||||||
chr6:147562694 | C | A | 30 | a0001c0001t0001g0339 a0001c0001t0011g0197 a0001c0001t0011g0208 others(27): Show |
30 | HG00140.hp1 HG00733.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.460-1700C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562694 | |||||||
chr6:147562777 | G | A | 1 | a0001c0001t0009g0271 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.460-1617G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562777 | |||||||
chr6:147562809 | G | A | 1 | a0001c0001t0002g0334 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.460-1585G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562809 | |||||||
chr6:147562821 | C | CA | 6 | a0001c0001t0003g0231 a0001c0001t0003g0296 a0001c0001t0009g0057 others(3): Show |
6 | HG01261.hp1 HG02451.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-1564dupA | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147562821 | ||||||
chr6:147562821 | C | CAA | 30 | a0001c0001t0001g0339 a0001c0001t0011g0197 a0001c0001t0011g0208 others(27): Show |
30 | HG00140.hp1 HG00733.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.460-1565_460-1564d others(4): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147562821 | ||||||
chr6:147562827 | A | T | 85 | a0001c0001t0002g0006 a0001c0001t0002g0035 a0001c0001t0002g0050 others(82): Show |
91 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.460-1567A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562827 | |||||||
chr6:147562831 | T | A | 205 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(202): Show |
213 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.460-1563T>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147562831 | |||||||
chr6:147563073 | G | A | 1 | a0001c0001t0104g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-1321G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563073 | |||||||
chr6:147563090 | C | A | 5 | a0001c0001t0003g0255 a0001c0001t0003g0278 a0001c0001t0003g0330 others(2): Show |
5 | HG01106.hp1 HG01361.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.460-1304C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563090 | |||||||
chr6:147563099 | A | T | 210 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(207): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.460-1295A>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563099 | |||||||
chr6:147563161 | GT | G | 30 | a0001c0001t0001g0339 a0001c0001t0011g0197 a0001c0001t0011g0208 others(27): Show |
30 | HG00140.hp1 HG00733.hp2 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.460-1232delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563161 | |||||||
chr6:147563347 | T | G | 1 | a0001c0002t0036g0132 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.460-1047T>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563347 | |||||||
chr6:147563356 | A | C | 10 | a0001c0001t0027g0036 a0001c0001t0027g0245 a0001c0001t0028g0297 others(7): Show |
10 | HG01884.hp1 HG02132.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.460-1038A>C | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563356 | |||||||
chr6:147563366 | G | T | 1 | a0001c0001t0104g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-1028G>T | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563366 | |||||||
chr6:147563469 | C | A | 3 | a0001c0001t0021g0049 a0001c0001t0021g0220 a0001c0001t0021g0262 |
3 | NA19000.hp1 NA19083.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.460-925C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563469 | |||||||
chr6:147563703 | A | G | 1 | a0001c0002t0014g0102 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.460-691A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563703 | |||||||
chr6:147563788 | ATACT | A | 3 | a0001c0001t0097g0065 a0001c0002t0054g0154 a0001c0002t0057g0169 |
3 | HG00140.hp1 HG00733.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.460-603_460-600del others(4): Show |
SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147563788 | ||||||
chr6:147563815 | C | A | 1 | a0001c0002t0008g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.460-579C>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563815 | |||||||
chr6:147563971 | G | A | 1 | a0001c0001t0005g0218 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.460-423G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147563971 | |||||||
chr6:147564104 | A | AT | 6 | a0001c0001t0027g0036 a0001c0001t0027g0245 a0001c0001t0028g0297 others(3): Show |
6 | HG01884.hp1 HG02723.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-281dupT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147564104 | ||||||
chr6:147564104 | AT | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0038 others(91): Show |
98 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.460-281delT | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr6 | 147564104 | ||||||
chr6:147564175 | A | G | 6 | a0001c0001t0027g0036 a0001c0001t0027g0245 a0001c0001t0028g0297 others(3): Show |
6 | HG01884.hp1 HG02723.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-219A>G | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147564175 | |||||||
chr6:147564197 | G | A | 6 | a0001c0001t0027g0036 a0001c0001t0027g0245 a0001c0001t0028g0297 others(3): Show |
6 | HG01884.hp1 HG02723.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.460-197G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147564197 | |||||||
chr6:147564288 | G | A | 1 | a0001c0001t0104g0244 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.460-106G>A | SAMD5 | ENSG00000203727.4 | transcript | ENST00000367474.2 | protein_coding | 1/1 | chr6 | 147564288 |