Item | Value |
---|---|
geneid | 9789 |
ensemblid | ENSG00000118363.13 |
hgncid | 28962 |
symbol | SPCS2 |
name | signal peptidase complex subunit 2 |
refseq_nuc | NM_014752.3 |
refseq_prot | NP_055567.2 |
ensembl_nuc | ENST00000263672.11 |
ensembl_prot | ENSP00000263672.6 |
mane_status | MANE Select |
chr | chr11 |
start | 74949266 |
end | 74979033 |
strand | + |
ver | v1.2 |
region | chr11:74949266-74979033 |
region5000 | chr11:74944266-74984033 |
regionname0 | SPCS2_chr11_74949266_74979033 |
regionname5000 | SPCS2_chr11_74944266_74984033 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 678 | 367 | 87 | 60 | 158 | 18 | 42 | SPCS2_chr11_74944266_74984033 | SPCS2 | ATGGC others(673): Show |
chr11 | 74944266 | 74984033 | ||
a0001c0002 | 0/0 | 678 | 11 | 11 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | ATGGC others(673): Show |
chr11 | 74944266 | 74984033 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2691 | 208 | 50 | 28 | 101 | 10 | 18 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0002 | 0/0 | 2691 | 105 | 24 | 20 | 40 | 6 | 15 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0003 | 0/0 | 2691 | 11 | 0 | 6 | 0 | 1 | 4 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0004 | 0/0 | 2688 | 10 | 0 | 1 | 9 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2683): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0005 | 0/1 | 2691 | 9 | 0 | 4 | 0 | 1 | 3 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0006 | 0/0 | 2691 | 9 | 9 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0007 | 0/0 | 2692 | 4 | 0 | 0 | 4 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2687): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0008 | 0/0 | 2691 | 3 | 3 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0009 | 0/0 | 2691 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0010 | 0/0 | 2691 | 2 | 0 | 0 | 0 | 0 | 2 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0011 | 0/0 | 2691 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0012 | 0/0 | 2691 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0013 | 0/0 | 2691 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
a0001c0001t0014 | 0/0 | 2691 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
a0001c0002t0001 | 0/0 | 2691 | 11 | 11 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | GAGAC others(2686): Show |
chr11 | 74944266 | 74984033 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0013 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0130 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0009 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0043 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0005g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0005g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0005g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0007g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0007g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0007g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0009g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0009g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0010g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0010g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0011g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0012g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0013g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0001t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0230 | EUR | GBR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0001 | EUR | GBR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | GBR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0251 | EUR | FIN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0236 | EUR | FIN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00408 | hp1 | a0001 | c0001 | t0012 | g0035 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01071 | hp2 | a0001 | c0001 | t0011 | g0009 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01169 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0071 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0219 | EUR | IBS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01884 | hp2 | a0001 | c0001 | t0014 | g0143 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02145 | hp1 | a0001 | c0001 | t0008 | g0066 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PEL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02155 | hp2 | a0001 | c0001 | t0007 | g0013 | EAS | CDX | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | CDX | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0046 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0280 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02615 | hp2 | a0001 | c0001 | t0008 | g0065 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0053 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0279 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02683 | hp2 | a0001 | c0001 | t0010 | g0244 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0282 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0278 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0281 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0045 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0055 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0285 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0064 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03239 | hp2 | a0001 | c0001 | t0010 | g0247 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | ESN | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0139 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0002 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0235 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0073 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0028 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0075 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | BEB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | STU | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | YRI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18965 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18984 | hp1 | a0001 | c0001 | t0013 | g0211 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18993 | hp1 | a0001 | c0001 | t0007 | g0096 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19010 | hp1 | a0001 | c0001 | t0009 | g0082 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | LWK | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | LWK | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19064 | hp1 | a0001 | c0001 | t0009 | g0030 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19090 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | YRI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ASW | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ASW | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0098 | EUR | TSI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | TSI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | GIH | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | GIH | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0099 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | USA | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | USA | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | USA | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | USA | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | LWK | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0081 | REF | REF | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0130 | REF | REF | SPCS2_chr11_74944266_74984033 | SPCS2 | chr11 | 74944266 | 74984033 |
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 |
---|
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74976995 | A | G | 1 | a0001c0002 | 11 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(8): Show |
synonymous_variant | LOW | c.633A>G | p.Glu211Glu | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 653/2691 | 633/681 | 211/226 | chr11 | 74976995 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74977098 | G | C | 1 | a0001c0001t0009 | 2 | NA19010.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*55G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 55 | chr11 | 74977098 | ||||||
chr11:74977590 | A | G | 1 | a0001c0001t0014 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*547A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 547 | chr11 | 74977590 | ||||||
chr11:74977658 | A | G | 1 | a0001c0001t0013 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*615A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 615 | chr11 | 74977658 | ||||||
chr11:74977888 | CAAT | C | 1 | a0001c0001t0004 | 10 | HG02148.hp2 NA18945.hp1 NA18946.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*851_*853delTAA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 851 | INFO_REALIGN_3_PRIME | chr11 | 74977888 | |||||
chr11:74978013 | A | C | 1 | a0001c0001t0006 | 9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*970A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 970 | chr11 | 74978013 | ||||||
chr11:74978313 | A | G | 1 | a0001c0001t0010 | 2 | HG02683.hp2 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1270A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1270 | chr11 | 74978313 | ||||||
chr11:74978327 | G | A | 5 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0010 others(2): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*1284G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1284 | chr11 | 74978327 | ||||||
chr11:74978376 | T | C | 1 | a0001c0001t0011 | 1 | HG01071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1333T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1333 | chr11 | 74978376 | ||||||
chr11:74978485 | T | TA | 1 | a0001c0001t0007 | 4 | HG02155.hp2 NA18965.hp2 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1443dupA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1444 | INFO_REALIGN_3_PRIME | chr11 | 74978485 | |||||
chr11:74978580 | C | T | 1 | a0001c0001t0008 | 3 | HG02145.hp1 HG02615.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1537C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1537 | chr11 | 74978580 | ||||||
chr11:74978605 | C | G | 1 | a0001c0001t0003 | 11 | HG01099.hp1 HG01106.hp1 HG01109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1562C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1562 | chr11 | 74978605 | ||||||
chr11:74978936 | T | C | 1 | a0001c0001t0005 | 8 | HG00099.hp2 HG00642.hp2 HG01167.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1893T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1893 | chr11 | 74978936 | ||||||
chr11:74979011 | A | G | 1 | a0001c0001t0012 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1968A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 5/5 | 1968 | chr11 | 74979011 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:74949459 | A | C | 90 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(87): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.114+60A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949459 | |||||||
chr11:74949488 | C | A | 1 | a0001c0001t0013g0211 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.114+89C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949488 | |||||||
chr11:74949505 | G | C | 1 | a0001c0001t0002g0212 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.114+106G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949505 | |||||||
chr11:74949540 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.114+141C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949540 | |||||||
chr11:74949541 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.114+142G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949541 | |||||||
chr11:74949586 | G | A | 71 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(68): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.114+187G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949586 | |||||||
chr11:74949622 | T | A | 1 | a0001c0001t0001g0048 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.114+223T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949622 | |||||||
chr11:74949673 | A | C | 5 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0284 others(2): Show |
7 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.114+274A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949673 | |||||||
chr11:74949705 | G | A | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0001g0023 others(9): Show |
13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+306G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949705 | |||||||
chr11:74949776 | C | G | 37 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(34): Show |
46 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.114+377C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949776 | |||||||
chr11:74949806 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.114+407G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949806 | |||||||
chr11:74949973 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.114+574C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74949973 | |||||||
chr11:74950039 | T | G | 2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | HG01433.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.114+640T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950039 | |||||||
chr11:74950057 | C | A | 1 | a0001c0001t0002g0215 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.114+658C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950057 | |||||||
chr11:74950065 | T | A | 90 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(87): Show |
117 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.114+666T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950065 | |||||||
chr11:74950086 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114+687G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950086 | |||||||
chr11:74950190 | C | T | 71 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(68): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.114+791C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950190 | |||||||
chr11:74950295 | A | G | 7 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0278 others(4): Show |
9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+896A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950295 | |||||||
chr11:74950611 | A | G | 3 | a0001c0001t0003g0175 a0001c0001t0003g0176 a0001c0001t0003g0177 |
3 | HG01109.hp1 HG01496.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.114+1212A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950611 | |||||||
chr11:74950641 | A | G | 7 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0278 others(4): Show |
9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+1242A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950641 | |||||||
chr11:74950659 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.114+1260C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950659 | |||||||
chr11:74950667 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.114+1268G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950667 | |||||||
chr11:74950890 | G | T | 79 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(76): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.114+1491G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950890 | |||||||
chr11:74950984 | T | A | 1 | a0001c0001t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.114+1585T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950984 | |||||||
chr11:74950993 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0174 |
3 | NA18974.hp2 NA18978.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.114+1594C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74950993 | |||||||
chr11:74951000 | G | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0173 |
4 | HG00639.hp2 HG01074.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+1601G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951000 | |||||||
chr11:74951023 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.114+1624T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951023 | |||||||
chr11:74951063 | G | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0171 others(1): Show |
11 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+1664G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951063 | |||||||
chr11:74951099 | G | T | 1 | a0001c0001t0002g0286 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.114+1700G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951099 | |||||||
chr11:74951109 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.114+1710A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951109 | |||||||
chr11:74951146 | G | A | 3 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 |
3 | HG01884.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114+1747G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951146 | |||||||
chr11:74951209 | A | G | 8 | a0001c0001t0002g0004 a0001c0001t0002g0021 a0001c0001t0002g0215 others(5): Show |
15 | HG00673.hp2 NA18941.hp2 NA18943.hp1 others(12): Show |
intron_variant | MODIFIER | c.114+1810A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951209 | |||||||
chr11:74951228 | A | C | 2 | a0001c0001t0002g0265 a0001c0001t0002g0266 |
2 | HG01106.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.114+1829A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951228 | |||||||
chr11:74951304 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0171 others(1): Show |
11 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+1905A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951304 | |||||||
chr11:74951322 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.114+1923G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951322 | |||||||
chr11:74951446 | G | A | 8 | a0001c0001t0002g0044 a0001c0001t0002g0209 a0001c0001t0002g0272 others(5): Show |
9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+2047G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951446 | |||||||
chr11:74951475 | A | G | 12 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0284 others(9): Show |
16 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.114+2076A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951475 | |||||||
chr11:74951536 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.114+2137C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951536 | |||||||
chr11:74951703 | G | A | 3 | a0001c0001t0008g0064 a0001c0001t0008g0065 a0001c0001t0008g0066 |
3 | HG02145.hp1 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.114+2304G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951703 | |||||||
chr11:74951759 | G | A | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0001g0023 others(9): Show |
13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+2360G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951759 | |||||||
chr11:74951767 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0217 a0001c0001t0002g0218 |
5 | HG01168.hp2 HG01169.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+2368G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951767 | |||||||
chr11:74951773 | G | A | 1 | a0001c0001t0002g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.114+2374G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951773 | |||||||
chr11:74951810 | C | CA | 7 | a0001c0001t0001g0039 a0001c0001t0001g0067 a0001c0001t0001g0171 others(4): Show |
8 | HG00639.hp2 HG02165.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+2430dupA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74951810 | ||||||
chr11:74951810 | C | CAAAAAA | 8 | a0001c0001t0002g0022 a0001c0001t0002g0218 a0001c0001t0002g0261 others(5): Show |
10 | HG01169.hp2 HG01255.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.114+2425_114+2430d others(8): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74951810 | ||||||
chr11:74951810 | C | CAAAAAAA | 58 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(55): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.114+2424_114+2430d others(9): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74951810 | ||||||
chr11:74951810 | C | CAAAAAAA others(1): Show |
14 | a0001c0001t0002g0044 a0001c0001t0002g0209 a0001c0001t0002g0220 others(11): Show |
15 | HG00735.hp1 HG00735.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+2423_114+2430d others(10): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74951810 | ||||||
chr11:74951810 | C | CAAAAAAA others(2): Show |
7 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0278 others(4): Show |
9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+2422_114+2430d others(11): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74951810 | ||||||
chr11:74951810 | CA | C | 19 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(16): Show |
20 | HG00323.hp1 HG01891.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.114+2430delA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74951810 | ||||||
chr11:74951928 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.114+2529G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951928 | |||||||
chr11:74951984 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.114+2585A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74951984 | |||||||
chr11:74952283 | C | T | 3 | a0001c0001t0008g0064 a0001c0001t0008g0065 a0001c0001t0008g0066 |
3 | HG02145.hp1 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.114+2884C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952283 | |||||||
chr11:74952443 | GT | G | 8 | a0001c0001t0002g0044 a0001c0001t0002g0209 a0001c0001t0002g0272 others(5): Show |
9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+3050delT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74952443 | ||||||
chr11:74952499 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.114+3100T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952499 | |||||||
chr11:74952507 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.114+3108A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952507 | |||||||
chr11:74952534 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0163 |
3 | NA18981.hp1 NA18988.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.114+3135C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952534 | |||||||
chr11:74952892 | T | C | 1 | a0001c0001t0003g0071 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.114+3493T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952892 | |||||||
chr11:74952916 | TGA | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0285 |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+3518_114+3519d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952916 | |||||||
chr11:74952919 | C | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0285 |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+3520C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952919 | |||||||
chr11:74952921 | T | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0285 |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+3522T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952921 | |||||||
chr11:74952922 | A | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0285 |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+3523A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952922 | |||||||
chr11:74952980 | G | A | 91 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(88): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.114+3581G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74952980 | |||||||
chr11:74953083 | C | G | 1 | a0001c0001t0002g0260 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.114+3684C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953083 | |||||||
chr11:74953217 | A | ATT | 5 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0280 others(2): Show |
7 | HG02451.hp2 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.114+3832_114+3833d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74953217 | ||||||
chr11:74953217 | AT | A | 20 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0072 others(17): Show |
21 | HG00408.hp2 HG01069.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.114+3833delT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74953217 | ||||||
chr11:74953256 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.114+3857A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953256 | |||||||
chr11:74953257 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.114+3858A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953257 | |||||||
chr11:74953274 | C | T | 1 | a0001c0001t0013g0211 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.114+3875C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953274 | |||||||
chr11:74953287 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.114+3888G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953287 | |||||||
chr11:74953459 | C | T | 9 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0154 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+4060C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953459 | |||||||
chr11:74953476 | C | T | 1 | a0001c0002t0001g0057 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.114+4077C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953476 | |||||||
chr11:74953681 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.114+4282T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953681 | |||||||
chr11:74953856 | A | T | 2 | a0001c0001t0006g0278 a0001c0001t0006g0279 |
2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.114+4457A>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953856 | |||||||
chr11:74953938 | G | C | 2 | a0001c0001t0002g0220 a0001c0001t0002g0226 |
2 | HG04184.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.114+4539G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74953938 | |||||||
chr11:74954271 | G | A | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0001g0023 others(9): Show |
13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+4872G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954271 | |||||||
chr11:74954397 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.114+4998G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954397 | |||||||
chr11:74954657 | G | C | 1 | a0001c0001t0002g0213 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.114+5258G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954657 | |||||||
chr11:74954699 | C | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0285 |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+5300C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954699 | |||||||
chr11:74954700 | G | A | 1 | a0001c0001t0003g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.114+5301G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954700 | |||||||
chr11:74954704 | C | T | 2 | a0001c0001t0002g0284 a0001c0001t0002g0286 |
2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.114+5305C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954704 | |||||||
chr11:74954895 | T | A | 1 | a0001c0001t0002g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.114+5496T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954895 | |||||||
chr11:74954943 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.114+5544C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74954943 | |||||||
chr11:74955047 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.114+5648A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955047 | |||||||
chr11:74955060 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.114+5661A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955060 | |||||||
chr11:74955387 | C | T | 8 | a0001c0001t0002g0044 a0001c0001t0002g0209 a0001c0001t0002g0272 others(5): Show |
9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+5988C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955387 | |||||||
chr11:74955440 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.114+6041G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955440 | |||||||
chr11:74955477 | A | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0285 |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+6078A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955477 | |||||||
chr11:74955642 | G | A | 8 | a0001c0001t0002g0044 a0001c0001t0002g0209 a0001c0001t0002g0272 others(5): Show |
9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+6243G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955642 | |||||||
chr11:74955709 | G | A | 8 | a0001c0001t0002g0044 a0001c0001t0002g0209 a0001c0001t0002g0272 others(5): Show |
9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+6310G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955709 | |||||||
chr11:74955814 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.114+6415T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955814 | |||||||
chr11:74955851 | A | AAT | 18 | a0001c0001t0001g0015 a0001c0001t0001g0036 a0001c0001t0001g0038 others(15): Show |
24 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.114+6487_114+6488d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATAT | 17 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0123 others(14): Show |
17 | HG00408.hp2 HG00639.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.114+6485_114+6488d others(6): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATAT | 15 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(12): Show |
15 | HG00639.hp1 HG00735.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.114+6483_114+6488d others(8): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(1): Show |
10 | a0001c0001t0001g0035 a0001c0001t0001g0117 a0001c0001t0001g0160 others(7): Show |
10 | HG00408.hp1 HG01106.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+6481_114+6488d others(10): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(3): Show |
19 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0034 others(16): Show |
25 | HG00140.hp1 HG00733.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.114+6479_114+6488d others(12): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(5): Show |
9 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(6): Show |
9 | HG00323.hp2 HG01243.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+6477_114+6488d others(14): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(7): Show |
5 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0002g0232 others(2): Show |
8 | HG00423.hp2 HG01069.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+6475_114+6488d others(16): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(9): Show |
5 | a0001c0001t0001g0032 a0001c0001t0001g0107 a0001c0001t0001g0108 others(2): Show |
6 | HG00140.hp2 HG01168.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+6473_114+6488d others(18): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(11): Show |
8 | a0001c0001t0001g0031 a0001c0001t0001g0063 a0001c0001t0001g0104 others(5): Show |
9 | HG00323.hp1 HG01256.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+6471_114+6488d others(20): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(13): Show |
10 | a0001c0001t0001g0013 a0001c0001t0001g0102 a0001c0001t0001g0103 others(7): Show |
11 | HG00099.hp1 HG00609.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+6469_114+6488d others(22): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(15): Show |
16 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(13): Show |
25 | HG00423.hp1 HG00733.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.114+6467_114+6488d others(24): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(17): Show |
17 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0040 others(14): Show |
29 | HG00099.hp2 HG01123.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.114+6465_114+6488d others(26): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(19): Show |
17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(14): Show |
24 | HG00609.hp1 HG01081.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.114+6463_114+6488d others(28): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(21): Show |
15 | a0001c0001t0001g0027 a0001c0001t0001g0060 a0001c0001t0001g0061 others(12): Show |
18 | HG00280.hp2 HG01099.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.114+6461_114+6488d others(30): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(23): Show |
15 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0048 others(12): Show |
17 | HG00642.hp2 HG01109.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.114+6459_114+6488d others(32): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(25): Show |
6 | a0001c0001t0001g0024 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
7 | HG00558.hp1 HG01081.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.114+6457_114+6488d others(34): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(27): Show |
2 | a0001c0001t0001g0076 a0001c0001t0003g0075 |
2 | HG04184.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.114+6455_114+6488d others(36): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | AATATATA others(37): Show |
1 | a0001c0001t0001g0074 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.114+6488_114+6489i others(46): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0264 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.114+6452_114+6453i others(15): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | |||||||
chr11:74955851 | A | ATATATAT others(8): Show |
1 | a0001c0001t0002g0259 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.114+6452_114+6453i others(17): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | |||||||
chr11:74955851 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0181 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.114+6452_114+6453i others(21): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | |||||||
chr11:74955851 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0150 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.114+6452_114+6453i others(23): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | |||||||
chr11:74955851 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01952.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.114+6452_114+6453i others(25): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | |||||||
chr11:74955851 | A | ATATATAT others(18): Show |
3 | a0001c0001t0001g0208 a0001c0001t0006g0282 a0001c0002t0001g0056 |
3 | HG01891.hp1 HG02723.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.114+6452_114+6453i others(27): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | |||||||
chr11:74955851 | A | ATATATAT others(20): Show |
2 | a0001c0001t0001g0147 a0001c0001t0004g0146 |
2 | NA18975.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.114+6452_114+6453i others(29): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | |||||||
chr11:74955851 | A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0145 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.114+6452_114+6453i others(31): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | |||||||
chr11:74955851 | A | T | 1 | a0001c0001t0001g0151 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.114+6452A>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955851 | |||||||
chr11:74955851 | AAT | A | 6 | a0001c0001t0001g0068 a0001c0001t0002g0020 a0001c0001t0003g0177 others(3): Show |
8 | HG02145.hp1 HG02615.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+6487_114+6488d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | AATAT | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0133 a0001c0001t0002g0258 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+6485_114+6488d others(6): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | AATATAT | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
6 | HG02818.hp1 NA18966.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.114+6483_114+6488d others(8): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | AATATATA others(1): Show |
A | 9 | a0001c0001t0001g0136 a0001c0001t0001g0206 a0001c0001t0002g0004 others(6): Show |
14 | HG00673.hp2 HG01981.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.114+6481_114+6488d others(10): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | AATATATA others(3): Show |
A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0171 a0001c0001t0001g0207 |
3 | HG02080.hp1 HG02451.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.114+6479_114+6488d others(12): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | AATATATA others(5): Show |
A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0138 others(1): Show |
11 | HG02040.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.114+6477_114+6488d others(14): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | AATATATA others(7): Show |
A | 9 | a0001c0001t0002g0044 a0001c0001t0002g0209 a0001c0001t0002g0272 others(6): Show |
10 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+6475_114+6488d others(16): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | AATATATA others(9): Show |
A | 1 | a0001c0001t0001g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.114+6473_114+6488d others(18): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | AATATATA others(11): Show |
A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0014g0143 |
3 | HG00544.hp1 HG01884.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.114+6471_114+6488d others(20): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | AATATATA others(13): Show |
A | 1 | a0001c0001t0001g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.114+6469_114+6488d others(22): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | AATATATA others(15): Show |
A | 6 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0285 others(3): Show |
8 | HG02258.hp1 HG02486.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+6467_114+6488d others(24): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955851 | AATATATA others(21): Show |
A | 2 | a0001c0001t0002g0284 a0001c0001t0002g0286 |
2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.114+6461_114+6488d others(30): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955851 | ||||||
chr11:74955884 | A | ATATATAT others(23): Show |
1 | a0001c0002t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.114+6488_114+6489i others(32): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955884 | ||||||
chr11:74955884 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0094 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.114+6488_114+6489i others(30): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955884 | ||||||
chr11:74955884 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0100 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.114+6488_114+6489i others(28): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74955884 | ||||||
chr11:74955887 | T | TATATATA others(21): Show |
1 | a0001c0001t0003g0099 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.114+6488_114+6489i others(30): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955887 | |||||||
chr11:74955925 | C | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0285 |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+6526C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955925 | |||||||
chr11:74955965 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.114+6566A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74955965 | |||||||
chr11:74956057 | A | G | 3 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0274 |
3 | HG01884.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114+6658A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74956057 | |||||||
chr11:74956221 | A | G | 2 | a0001c0001t0002g0228 a0001c0001t0002g0231 |
2 | HG01361.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.114+6822A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74956221 | |||||||
chr11:74956536 | A | AT | 24 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0001g0058 others(21): Show |
27 | HG00639.hp2 HG01074.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.114+7141dupT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74956536 | ||||||
chr11:74956836 | C | A | 8 | a0001c0001t0002g0044 a0001c0001t0002g0209 a0001c0001t0002g0272 others(5): Show |
9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+7437C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74956836 | |||||||
chr11:74956858 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.114+7459G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74956858 | |||||||
chr11:74956950 | A | G | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0001g0023 others(9): Show |
13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.114+7551A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74956950 | |||||||
chr11:74956968 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.114+7569C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74956968 | |||||||
chr11:74957028 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.114+7629C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74957028 | |||||||
chr11:74957036 | G | C | 91 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(88): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.114+7637G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74957036 | |||||||
chr11:74957054 | G | A | 9 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0154 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.114+7655G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74957054 | |||||||
chr11:74957089 | A | C | 1 | a0001c0001t0001g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.114+7690A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74957089 | |||||||
chr11:74957611 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.115-7423A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74957611 | |||||||
chr11:74957968 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.115-7066A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74957968 | |||||||
chr11:74958015 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0207 |
2 | HG02698.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.115-7019T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958015 | |||||||
chr11:74958129 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.115-6905C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958129 | |||||||
chr11:74958224 | A | G | 4 | a0001c0001t0003g0087 a0001c0001t0003g0099 a0001c0001t0003g0118 others(1): Show |
4 | HG01099.hp1 HG01106.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-6810A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958224 | |||||||
chr11:74958349 | T | G | 71 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(68): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.115-6685T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958349 | |||||||
chr11:74958454 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0171 others(1): Show |
11 | HG02258.hp2 HG02280.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-6580G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958454 | |||||||
chr11:74958509 | T | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0140 |
2 | HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.115-6525T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958509 | |||||||
chr11:74958605 | A | G | 2 | a0001c0001t0002g0234 a0001c0001t0002g0243 |
2 | HG01261.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.115-6429A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958605 | |||||||
chr11:74958981 | T | G | 2 | a0001c0001t0002g0284 a0001c0001t0002g0286 |
2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.115-6053T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74958981 | |||||||
chr11:74959084 | C | T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0068 a0001c0001t0001g0069 others(6): Show |
11 | HG00639.hp2 HG01074.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.115-5950C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959084 | |||||||
chr11:74959285 | C | G | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.115-5749C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959285 | |||||||
chr11:74959366 | G | A | 3 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0285 |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-5668G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959366 | |||||||
chr11:74959429 | A | G | 7 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0278 others(4): Show |
9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-5605A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959429 | |||||||
chr11:74959457 | A | G | 5 | a0001c0001t0001g0078 a0001c0001t0001g0092 a0001c0001t0001g0103 others(2): Show |
5 | HG01884.hp2 NA18974.hp1 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.115-5577A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959457 | |||||||
chr11:74959461 | C | T | 9 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0154 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-5573C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959461 | |||||||
chr11:74959640 | C | T | 2 | a0001c0001t0006g0278 a0001c0001t0006g0279 |
2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.115-5394C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959640 | |||||||
chr11:74959741 | G | A | 12 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0284 others(9): Show |
16 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.115-5293G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959741 | |||||||
chr11:74959766 | G | C | 1 | a0001c0001t0001g0093 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.115-5268G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959766 | |||||||
chr11:74959814 | A | G | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0001g0023 others(9): Show |
13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.115-5220A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74959814 | |||||||
chr11:74960055 | T | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(77): Show |
100 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.115-4979T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960055 | |||||||
chr11:74960289 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.115-4745G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960289 | |||||||
chr11:74960312 | C | G | 5 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0091 others(2): Show |
6 | NA18612.hp1 NA18954.hp2 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-4722C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960312 | |||||||
chr11:74960313 | A | G | 1 | a0001c0001t0002g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.115-4721A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960313 | |||||||
chr11:74960440 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.115-4594G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960440 | |||||||
chr11:74960440 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.115-4594G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960440 | |||||||
chr11:74960441 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.115-4593G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960441 | |||||||
chr11:74960502 | C | CT | 79 | a0001c0001t0001g0101 a0001c0001t0002g0004 a0001c0001t0002g0008 others(76): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.115-4518dupT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74960502 | ||||||
chr11:74960523 | TTA | T | 8 | a0001c0001t0002g0044 a0001c0001t0002g0209 a0001c0001t0002g0272 others(5): Show |
9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-4510_115-4509d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960523 | |||||||
chr11:74960601 | G | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0097 a0001c0001t0001g0121 others(2): Show |
6 | HG01981.hp2 NA18970.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-4433G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960601 | |||||||
chr11:74960604 | C | CT | 91 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(88): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.115-4427dupT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74960604 | ||||||
chr11:74960677 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0171 |
3 | HG02258.hp2 HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.115-4357A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960677 | |||||||
chr11:74960868 | T | A | 12 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0284 others(9): Show |
16 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.115-4166T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960868 | |||||||
chr11:74960891 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.115-4143T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74960891 | |||||||
chr11:74961035 | TA | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0111 others(7): Show |
17 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.115-3985delA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74961035 | ||||||
chr11:74961079 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.115-3955C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961079 | |||||||
chr11:74961123 | A | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.115-3911A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961123 | |||||||
chr11:74961240 | G | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0285 |
4 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-3794G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961240 | |||||||
chr11:74961494 | G | A | 7 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0278 others(4): Show |
9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-3540G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961494 | |||||||
chr11:74961517 | T | G | 1 | a0001c0001t0001g0190 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.115-3517T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961517 | |||||||
chr11:74961517 | TTTG | T | 11 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0154 others(8): Show |
12 | HG01243.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.115-3502_115-3500d others(5): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74961517 | ||||||
chr11:74961529 | GTTGT | G | 4 | a0001c0001t0001g0058 a0001c0001t0001g0186 a0001c0001t0002g0284 others(1): Show |
4 | HG00558.hp1 HG02145.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.115-3482_115-3479d others(6): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74961529 | ||||||
chr11:74961574 | TCTGTTCA others(42): Show |
T | 1 | a0001c0001t0002g0219 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.115-3457_115-3409d others(51): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74961574 | ||||||
chr11:74961593 | G | A | 1 | a0001c0001t0002g0263 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.115-3441G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961593 | |||||||
chr11:74961726 | C | T | 1 | a0001c0001t0002g0268 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.115-3308C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961726 | |||||||
chr11:74961734 | G | A | 9 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0154 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-3300G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961734 | |||||||
chr11:74961765 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(203): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.115-3269T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74961765 | |||||||
chr11:74962131 | T | C | 1 | a0001c0001t0010g0244 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.115-2903T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962131 | |||||||
chr11:74962225 | A | G | 79 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(76): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.115-2809A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962225 | |||||||
chr11:74962395 | C | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0093 a0001c0001t0001g0135 |
3 | HG02818.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.115-2639C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962395 | |||||||
chr11:74962396 | T | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0093 a0001c0001t0001g0135 |
3 | HG02818.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.115-2638T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962396 | |||||||
chr11:74962548 | CA | C | 77 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0062 others(74): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.115-2472delA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74962548 | ||||||
chr11:74962579 | C | G | 1 | a0001c0001t0002g0230 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.115-2455C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962579 | |||||||
chr11:74962582 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.115-2452G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962582 | |||||||
chr11:74962710 | T | C | 1 | a0001c0001t0002g0284 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-2324T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74962710 | |||||||
chr11:74963253 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG00544.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.115-1781A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74963253 | |||||||
chr11:74963544 | ATTGT | A | 4 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0285 others(1): Show |
6 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.115-1467_115-1464d others(6): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74963544 | ||||||
chr11:74963567 | G | A | 7 | a0001c0002t0001g0023 a0001c0002t0001g0049 a0001c0002t0001g0050 others(4): Show |
8 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.115-1467G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74963567 | |||||||
chr11:74963567 | GTTTA | G | 33 | a0001c0001t0001g0025 a0001c0001t0001g0047 a0001c0001t0001g0097 others(30): Show |
36 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.115-1447_115-1444d others(6): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | 74963567 | ||||||
chr11:74963571 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(140): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.115-1463A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74963571 | |||||||
chr11:74963575 | A | G | 11 | a0001c0001t0001g0110 a0001c0001t0002g0044 a0001c0001t0002g0209 others(8): Show |
12 | HG01099.hp2 HG02055.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.115-1459A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74963575 | |||||||
chr11:74963610 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.115-1424A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74963610 | |||||||
chr11:74963907 | A | G | 1 | a0001c0001t0002g0284 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.115-1127A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74963907 | |||||||
chr11:74964037 | G | A | 1 | a0001c0001t0003g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.115-997G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74964037 | |||||||
chr11:74964787 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.115-247G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74964787 | |||||||
chr11:74964822 | T | G | 8 | a0001c0001t0002g0044 a0001c0001t0002g0209 a0001c0001t0002g0272 others(5): Show |
9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-212T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74964822 | |||||||
chr11:74964851 | T | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(77): Show |
100 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.115-183T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74964851 | |||||||
chr11:74964986 | G | A | 3 | a0001c0001t0008g0064 a0001c0001t0008g0065 a0001c0001t0008g0066 |
3 | HG02145.hp1 HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.115-48G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 1/4 | chr11 | 74964986 | |||||||
chr11:74965306 | A | G | 9 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0154 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.198+189A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 2/4 | chr11 | 74965306 | |||||||
chr11:74965358 | A | G | 1 | a0001c0001t0014g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.198+241A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 2/4 | chr11 | 74965358 | |||||||
chr11:74965374 | A | C | 79 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(76): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.198+257A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 2/4 | chr11 | 74965374 | |||||||
chr11:74965467 | G | T | 91 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(88): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.199-296G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 2/4 | chr11 | 74965467 | |||||||
chr11:74965503 | T | C | 1 | a0001c0001t0014g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.199-260T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 2/4 | chr11 | 74965503 | |||||||
chr11:74965749 | G | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.199-14G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 2/4 | chr11 | 74965749 | |||||||
chr11:74965962 | A | G | 1 | a0001c0001t0003g0099 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.359+39A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74965962 | |||||||
chr11:74966191 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.359+268G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966191 | |||||||
chr11:74966203 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.359+280G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966203 | |||||||
chr11:74966394 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.359+471T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966394 | |||||||
chr11:74966415 | T | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.359+492T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966415 | |||||||
chr11:74966495 | G | T | 1 | a0001c0001t0001g0185 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.359+572G>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966495 | |||||||
chr11:74966773 | C | CG | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.359+850_359+851ins others(1): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966773 | |||||||
chr11:74966773 | C | CGT | 5 | a0001c0001t0001g0072 a0001c0001t0001g0078 a0001c0001t0001g0163 others(2): Show |
5 | NA18946.hp2 NA18949.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.359+850_359+851ins others(2): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966773 | |||||||
chr11:74966846 | G | A | 4 | a0001c0001t0002g0245 a0001c0001t0002g0250 a0001c0001t0002g0254 others(1): Show |
4 | HG00544.hp2 HG02027.hp2 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.359+923G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966846 | |||||||
chr11:74966957 | G | A | 7 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0278 others(4): Show |
9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.359+1034G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74966957 | |||||||
chr11:74967044 | A | T | 1 | a0001c0001t0002g0277 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.359+1121A>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967044 | |||||||
chr11:74967134 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.359+1211G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967134 | |||||||
chr11:74967157 | T | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.359+1234T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967157 | |||||||
chr11:74967158 | T | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.359+1235T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967158 | |||||||
chr11:74967189 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.359+1266C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967189 | |||||||
chr11:74967437 | T | TA | 91 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(88): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.359+1514_359+1515i others(3): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967437 | |||||||
chr11:74967479 | G | A | 2 | a0001c0001t0002g0284 a0001c0001t0002g0286 |
2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.359+1556G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967479 | |||||||
chr11:74967529 | C | T | 12 | a0001c0001t0001g0015 a0001c0001t0001g0047 a0001c0001t0001g0068 others(9): Show |
14 | HG00639.hp2 HG01074.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.359+1606C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967529 | |||||||
chr11:74967530 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.359+1607A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967530 | |||||||
chr11:74967592 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.359+1669T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967592 | |||||||
chr11:74967679 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.359+1756G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967679 | |||||||
chr11:74967680 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.359+1757C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967680 | |||||||
chr11:74967747 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.360-1818C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74967747 | |||||||
chr11:74968010 | T | C | 1 | a0001c0001t0002g0263 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.360-1555T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968010 | |||||||
chr11:74968033 | G | A | 2 | a0001c0001t0008g0064 a0001c0001t0008g0066 |
2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.360-1532G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968033 | |||||||
chr11:74968138 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0076 a0001c0001t0001g0091 others(2): Show |
6 | NA18612.hp1 NA18954.hp2 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.360-1427C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968138 | |||||||
chr11:74968258 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.360-1307T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968258 | |||||||
chr11:74968276 | G | A | 65 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(62): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.360-1289G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968276 | |||||||
chr11:74968385 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.360-1180G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968385 | |||||||
chr11:74968435 | C | G | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0001g0023 others(9): Show |
13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.360-1130C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968435 | |||||||
chr11:74968446 | C | G | 1 | a0001c0001t0006g0279 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.360-1119C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968446 | |||||||
chr11:74968518 | G | GT | 24 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0069 others(21): Show |
25 | HG00544.hp2 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.360-1032dupT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 74968518 | ||||||
chr11:74968518 | GT | G | 23 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0002g0022 others(20): Show |
27 | HG01099.hp2 HG01884.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.360-1032delT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr11 | 74968518 | ||||||
chr11:74968523 | T | G | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.360-1042T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968523 | |||||||
chr11:74968578 | C | T | 79 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(76): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.360-987C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968578 | |||||||
chr11:74968714 | G | C | 2 | a0001c0001t0006g0278 a0001c0001t0006g0279 |
2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.360-851G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968714 | |||||||
chr11:74968816 | C | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0285 |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.360-749C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74968816 | |||||||
chr11:74969137 | A | G | 1 | a0001c0001t0007g0096 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.360-428A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 3/4 | chr11 | 74969137 | |||||||
chr11:74969755 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.494+56T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74969755 | |||||||
chr11:74969836 | T | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0174 |
3 | NA18974.hp2 NA18978.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.494+137T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74969836 | |||||||
chr11:74969945 | A | G | 7 | a0001c0002t0001g0023 a0001c0002t0001g0049 a0001c0002t0001g0050 others(4): Show |
8 | HG01891.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.494+246A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74969945 | |||||||
chr11:74970061 | A | G | 35 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
44 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.494+362A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970061 | |||||||
chr11:74970226 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494+527C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970226 | |||||||
chr11:74970345 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.494+646A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970345 | |||||||
chr11:74970364 | A | G | 79 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(76): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.494+665A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970364 | |||||||
chr11:74970645 | C | T | 9 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0154 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.494+946C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970645 | |||||||
chr11:74970802 | C | T | 8 | a0001c0001t0002g0044 a0001c0001t0002g0209 a0001c0001t0002g0272 others(5): Show |
9 | HG01099.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.494+1103C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970802 | |||||||
chr11:74970873 | A | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0093 a0001c0001t0001g0135 |
3 | HG02818.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.494+1174A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970873 | |||||||
chr11:74970908 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.494+1209A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970908 | |||||||
chr11:74970984 | A | T | 1 | a0001c0001t0002g0236 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.494+1285A>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74970984 | |||||||
chr11:74971085 | T | G | 6 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0232 others(3): Show |
6 | HG00323.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.494+1386T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971085 | |||||||
chr11:74971200 | A | G | 1 | a0001c0001t0001g0208 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.494+1501A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971200 | |||||||
chr11:74971441 | C | A | 9 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0154 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.494+1742C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971441 | |||||||
chr11:74971583 | C | G | 1 | a0001c0001t0001g0169 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.494+1884C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971583 | |||||||
chr11:74971617 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.494+1918A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971617 | |||||||
chr11:74971749 | A | G | 5 | a0001c0001t0002g0237 a0001c0001t0002g0239 a0001c0001t0002g0248 others(2): Show |
5 | HG02615.hp1 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+2050A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971749 | |||||||
chr11:74971749 | AT | A | 5 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0284 others(2): Show |
7 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.494+2054delT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74971749 | ||||||
chr11:74971801 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.494+2102T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74971801 | |||||||
chr11:74972113 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0116 |
2 | HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.494+2414C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972113 | |||||||
chr11:74972119 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0242 |
4 | NA18942.hp2 NA18949.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+2420C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972119 | |||||||
chr11:74972127 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.494+2428C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972127 | |||||||
chr11:74972158 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.494+2459C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972158 | |||||||
chr11:74972185 | C | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0285 |
5 | HG02895.hp2 HG02897.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+2486C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972185 | |||||||
chr11:74972197 | C | A | 79 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(76): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.494+2498C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972197 | |||||||
chr11:74972200 | G | C | 79 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(76): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.494+2501G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972200 | |||||||
chr11:74972570 | C | T | 7 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0278 others(4): Show |
9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.494+2871C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972570 | |||||||
chr11:74972720 | CT | C | 8 | a0001c0001t0001g0115 a0001c0001t0001g0147 a0001c0001t0001g0156 others(5): Show |
8 | HG00609.hp2 HG02976.hp2 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.494+3035delT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74972720 | ||||||
chr11:74972738 | C | T | 79 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(76): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.494+3039C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972738 | |||||||
chr11:74972878 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.494+3179T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972878 | |||||||
chr11:74972878 | T | TTA | 5 | a0001c0001t0001g0112 a0001c0001t0001g0156 a0001c0001t0001g0160 others(2): Show |
5 | HG01516.hp2 HG01517.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+3195_494+3196d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74972878 | ||||||
chr11:74972878 | TTA | T | 10 | a0001c0001t0001g0015 a0001c0001t0001g0068 a0001c0001t0001g0070 others(7): Show |
12 | HG00639.hp2 HG01074.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.494+3195_494+3196d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74972878 | ||||||
chr11:74972893 | TA | T | 73 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0047 others(70): Show |
101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.494+3195delA | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972893 | |||||||
chr11:74972894 | A | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0144 a0001c0001t0002g0255 others(1): Show |
4 | HG02109.hp2 HG03041.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+3195A>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972894 | |||||||
chr11:74972894 | AT | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(103): Show |
128 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.494+3206delT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74972894 | ||||||
chr11:74972894 | ATT | A | 8 | a0001c0001t0002g0286 a0001c0001t0006g0045 a0001c0001t0006g0046 others(5): Show |
10 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.494+3205_494+3206d others(4): Show |
SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74972894 | ||||||
chr11:74972896 | T | A | 53 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(50): Show |
65 | HG00408.hp2 HG00558.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.494+3197T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972896 | |||||||
chr11:74972897 | T | A | 1 | a0001c0001t0001g0140 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.494+3198T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972897 | |||||||
chr11:74972898 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.494+3199T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972898 | |||||||
chr11:74972948 | C | A | 91 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(88): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.494+3249C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972948 | |||||||
chr11:74972951 | A | G | 2 | a0001c0001t0002g0284 a0001c0001t0002g0286 |
2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.494+3252A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74972951 | |||||||
chr11:74973083 | A | G | 3 | a0001c0001t0002g0238 a0001c0001t0002g0256 a0001c0001t0002g0262 |
3 | HG00642.hp1 HG00733.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.494+3384A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973083 | |||||||
chr11:74973246 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.494+3547T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973246 | |||||||
chr11:74973274 | G | A | 2 | a0001c0001t0006g0278 a0001c0001t0006g0279 |
2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.494+3575G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973274 | |||||||
chr11:74973517 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.495-3340A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973517 | |||||||
chr11:74973596 | A | G | 5 | a0001c0001t0001g0162 a0001c0001t0008g0064 a0001c0001t0008g0065 others(2): Show |
5 | HG01884.hp2 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.495-3261A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973596 | |||||||
chr11:74973691 | T | G | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0001g0023 others(9): Show |
13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.495-3166T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973691 | |||||||
chr11:74973846 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.495-3011C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74973846 | |||||||
chr11:74974024 | T | C | 71 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(68): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.495-2833T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974024 | |||||||
chr11:74974111 | C | CT | 178 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(175): Show |
225 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.495-2735dupT | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | 74974111 | ||||||
chr11:74974228 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.495-2629A>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974228 | |||||||
chr11:74974276 | T | A | 9 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0154 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.495-2581T>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974276 | |||||||
chr11:74974307 | C | T | 3 | a0001c0001t0002g0044 a0001c0001t0002g0209 a0001c0001t0002g0275 |
4 | HG01099.hp2 HG02809.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.495-2550C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974307 | |||||||
chr11:74974314 | C | G | 1 | a0001c0001t0002g0224 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.495-2543C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974314 | |||||||
chr11:74974367 | G | A | 7 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0278 others(4): Show |
9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.495-2490G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974367 | |||||||
chr11:74974383 | C | T | 4 | a0001c0001t0002g0043 a0001c0001t0002g0251 a0001c0001t0002g0265 others(1): Show |
5 | HG00280.hp1 HG01106.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.495-2474C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974383 | |||||||
chr11:74974516 | C | T | 6 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0002g0232 others(3): Show |
6 | HG00323.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.495-2341C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974516 | |||||||
chr11:74974563 | C | T | 1 | a0001c0001t0003g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.495-2294C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974563 | |||||||
chr11:74974689 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0093 a0001c0001t0001g0135 |
3 | HG02818.hp1 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.495-2168G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974689 | |||||||
chr11:74974743 | T | G | 1 | a0001c0001t0001g0208 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.495-2114T>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974743 | |||||||
chr11:74974763 | A | T | 91 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0009 others(88): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.495-2094A>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974763 | |||||||
chr11:74974835 | G | C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0089 a0001c0001t0001g0114 others(3): Show |
6 | NA18951.hp2 NA18989.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.495-2022G>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974835 | |||||||
chr11:74974965 | C | G | 9 | a0001c0001t0001g0037 a0001c0001t0001g0060 a0001c0001t0001g0154 others(6): Show |
10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.495-1892C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974965 | |||||||
chr11:74974988 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.495-1869G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74974988 | |||||||
chr11:74975070 | G | A | 1 | a0001c0001t0002g0249 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.495-1787G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74975070 | |||||||
chr11:74975149 | C | G | 12 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0001g0023 others(9): Show |
13 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.495-1708C>G | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74975149 | |||||||
chr11:74975379 | C | T | 1 | a0001c0001t0003g0139 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.495-1478C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74975379 | |||||||
chr11:74975401 | C | T | 1 | a0001c0001t0003g0118 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.495-1456C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74975401 | |||||||
chr11:74975487 | T | C | 7 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0278 others(4): Show |
9 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.495-1370T>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74975487 | |||||||
chr11:74975878 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0095 |
2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.495-979C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74975878 | |||||||
chr11:74976013 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.495-844C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976013 | |||||||
chr11:74976180 | C | T | 12 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0284 others(9): Show |
16 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.495-677C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976180 | |||||||
chr11:74976211 | C | A | 12 | a0001c0001t0002g0022 a0001c0001t0002g0283 a0001c0001t0002g0284 others(9): Show |
16 | HG02451.hp2 HG02572.hp1 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.495-646C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976211 | |||||||
chr11:74976220 | C | T | 2 | a0001c0001t0002g0235 a0001c0001t0002g0236 |
2 | HG00323.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.495-637C>T | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976220 | |||||||
chr11:74976296 | A | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(201): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.495-561A>C | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976296 | |||||||
chr11:74976394 | G | A | 296 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(293): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.495-463G>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976394 | |||||||
chr11:74976434 | C | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | HG02896.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.495-423C>A | SPCS2 | ENSG00000118363.13 | transcript | ENST00000263672.11 | protein_coding | 4/4 | chr11 | 74976434 |