geneid | 10943 |
---|---|
ensemblid | ENSG00000005302.19 |
hgncid | 7370 |
symbol | MSL3 |
name | MSL complex subunit 3 |
refseq_nuc | NM_078629.4 |
refseq_prot | NP_523353.2 |
ensembl_nuc | ENST00000312196.10 |
ensembl_prot | ENSP00000312244.4 |
mane_status | MANE Select |
chr | chrX |
start | 11758237 |
end | 11775772 |
strand | + |
ver | v1.2 |
region | chrX:11758237-11775772 |
region5000 | chrX:11753237-11780772 |
regionname0 | MSL3_chrX_11758237_11775772 |
regionname5000 | MSL3_chrX_11753237_11780772 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 521 | 293 | 80 | 52 | 120 | 13 | 26 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0002 | 0/0 | 521 | 2 | 0 | 0 | 0 | 0 | 2 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0003 | 0/0 | 422 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0004 | 0/0 | 503 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1566 | 274 | 66 | 47 | 120 | 13 | 26 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
c0002 | 0/0 | 1566 | 10 | 5 | 5 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
c0003 | 0/0 | 1566 | 7 | 7 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
c0004 | 0/0 | 1566 | 2 | 0 | 0 | 0 | 0 | 2 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
c0005 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
c0006 | 0/0 | 1566 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
c0007 | 0/0 | 1567 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
c0008 | 0/0 | 1566 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 721 | 251 | 78 | 48 | 86 | 12 | 25 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
t0002 | 0/0 | 721 | 44 | 2 | 5 | 33 | 1 | 3 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
t0003 | 0/0 | 723 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
t0004 | 0/0 | 721 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 100 | 8 | 20 | 54 | 5 | 13 | MSL3_chrX_11753237_11780772 | MSL3 |
g0002 | 0/0 | 27 | 1 | 4 | 21 | 1 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0003 | 0/0 | 9 | 5 | 2 | 0 | 0 | 2 | MSL3_chrX_11753237_11780772 | MSL3 |
g0004 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0005 | 1/0 | 8 | 1 | 4 | 0 | 1 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
g0006 | 0/0 | 8 | 3 | 4 | 0 | 1 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0016 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSL3_chrX_11753237_11780772 | MSL3 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | a0001 | c0001 | 1/1 | 274 | 66 | 47 | 120 | 13 | 26 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0001c0002 | a0001 | c0002 | 0/0 | 10 | 5 | 5 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0001c0003 | a0001 | c0003 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0001c0005 | a0001 | c0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0001c0008 | a0001 | c0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0002c0004 | a0002 | c0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0003c0007 | a0003 | c0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0004c0006 | a0004 | c0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 229 | 64 | 42 | 86 | 12 | 23 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 44 | 2 | 5 | 33 | 1 | 3 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 10 | 5 | 5 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0001c0008t0001 | a0001 | c0008 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0002c0004t0001 | a0002 | c0004 | t0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0003c0007t0001 | a0003 | c0007 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
a0004c0006t0003 | a0004 | c0006 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 | copy fasta |
actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 94 | 7 | 20 | 51 | 5 | 11 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 6 | 4 | 0 | 0 | 0 | 2 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 1/0 | 8 | 1 | 4 | 0 | 1 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 8 | 3 | 4 | 0 | 1 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0001 | a0001 | c0001 | t0002 | g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0002 | a0001 | c0001 | t0002 | g0002 | 0/0 | 26 | 1 | 4 | 20 | 1 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0007 | a0001 | c0001 | t0002 | g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0023 | a0001 | c0001 | t0002 | g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0032 | a0001 | c0001 | t0002 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0033 | a0001 | c0001 | t0002 | g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0041 | a0001 | c0001 | t0002 | g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0043 | a0001 | c0001 | t0002 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0044 | a0001 | c0001 | t0002 | g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0045 | a0001 | c0001 | t0002 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0056 | a0001 | c0001 | t0002 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0064 | a0001 | c0001 | t0002 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0065 | a0001 | c0001 | t0002 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0072 | a0001 | c0001 | t0002 | g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0073 | a0001 | c0001 | t0002 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0002g0093 | a0001 | c0001 | t0002 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0001t0004g0002 | a0001 | c0001 | t0004 | g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0002t0001g0003 | a0001 | c0002 | t0001 | g0003 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0002t0001g0015 | a0001 | c0002 | t0001 | g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0002t0001g0019 | a0001 | c0002 | t0001 | g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0002t0001g0022 | a0001 | c0002 | t0001 | g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0003t0001g0011 | a0001 | c0003 | t0001 | g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0003t0001g0057 | a0001 | c0003 | t0001 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0003t0001g0060 | a0001 | c0003 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0003t0001g0061 | a0001 | c0003 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0005t0001g0001 | a0001 | c0005 | t0001 | g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0001c0008t0001g0082 | a0001 | c0008 | t0001 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0002c0004t0001g0001 | a0002 | c0004 | t0001 | g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MSL3_chrX_11753237_11780772 | MSL3 |
a0003c0007t0001g0094 | a0003 | c0007 | t0001 | g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
a0004c0006t0003g0051 | a0004 | c0006 | t0003 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MSL3_chrX_11753237_11780772 | MSL3 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MSL3_chrX_11753237_11780772 | MSL3 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | MSL3_chrX_11753237_11780772 | MSL3 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | MSL3_chrX_11753237_11780772 | MSL3 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | MSL3_chrX_11753237_11780772 | MSL3 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | MSL3_chrX_11753237_11780772 | MSL3 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | MSL3_chrX_11753237_11780772 | MSL3 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | MSL3_chrX_11753237_11780772 | MSL3 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | MSL3_chrX_11753237_11780772 | MSL3 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MSL3_chrX_11753237_11780772 | MSL3 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | MSL3_chrX_11753237_11780772 | MSL3 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | MSL3_chrX_11753237_11780772 | MSL3 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MSL3_chrX_11753237_11780772 | MSL3 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | MSL3_chrX_11753237_11780772 | MSL3 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01168 | hp1 | a0003 | c0007 | t0001 | g0094 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MSL3_chrX_11753237_11780772 | MSL3 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MSL3_chrX_11753237_11780772 | MSL3 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MSL3_chrX_11753237_11780772 | MSL3 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MSL3_chrX_11753237_11780772 | MSL3 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | MSL3_chrX_11753237_11780772 | MSL3 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | MSL3_chrX_11753237_11780772 | MSL3 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MSL3_chrX_11753237_11780772 | MSL3 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CDX | MSL3_chrX_11753237_11780772 | MSL3 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MSL3_chrX_11753237_11780772 | MSL3 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | MSL3_chrX_11753237_11780772 | MSL3 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MSL3_chrX_11753237_11780772 | MSL3 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02280 | hp1 | a0001 | c0008 | t0001 | g0082 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | MSL3_chrX_11753237_11780772 | MSL3 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02809 | hp2 | a0001 | c0005 | t0001 | g0001 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0060 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03041 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0057 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | MSL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | MSL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MSL3_chrX_11753237_11780772 | MSL3 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | MSL3_chrX_11753237_11780772 | MSL3 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MSL3_chrX_11753237_11780772 | MSL3 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | MSL3_chrX_11753237_11780772 | MSL3 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | MSL3_chrX_11753237_11780772 | MSL3 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | MSL3_chrX_11753237_11780772 | MSL3 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | MSL3_chrX_11753237_11780772 | MSL3 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | STU | MSL3_chrX_11753237_11780772 | MSL3 |
HG04184 | hp1 | a0002 | c0004 | t0001 | g0001 | SAS | BEB | MSL3_chrX_11753237_11780772 | MSL3 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MSL3_chrX_11753237_11780772 | MSL3 |
HG04199 | hp1 | a0002 | c0004 | t0001 | g0001 | SAS | STU | MSL3_chrX_11753237_11780772 | MSL3 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MSL3_chrX_11753237_11780772 | MSL3 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | STU | MSL3_chrX_11753237_11780772 | MSL3 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | MSL3_chrX_11753237_11780772 | MSL3 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHB | MSL3_chrX_11753237_11780772 | MSL3 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MSL3_chrX_11753237_11780772 | MSL3 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | YRI | MSL3_chrX_11753237_11780772 | MSL3 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | YRI | MSL3_chrX_11753237_11780772 | MSL3 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19006 | hp1 | a0004 | c0006 | t0003 | g0051 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | MSL3_chrX_11753237_11780772 | MSL3 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MSL3_chrX_11753237_11780772 | MSL3 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | MSL3_chrX_11753237_11780772 | MSL3 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MSL3_chrX_11753237_11780772 | MSL3 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | MSL3_chrX_11753237_11780772 | MSL3 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ASW | MSL3_chrX_11753237_11780772 | MSL3 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | MSL3_chrX_11753237_11780772 | MSL3 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | MSL3_chrX_11753237_11780772 | MSL3 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | MSL3_chrX_11753237_11780772 | MSL3 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MSL3_chrX_11753237_11780772 | MSL3 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MSL3_chrX_11753237_11780772 | MSL3 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | MSL3_chrX_11753237_11780772 | MSL3 |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | USA | MSL3_chrX_11753237_11780772 | MSL3 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0061 | AFR | USA | MSL3_chrX_11753237_11780772 | MSL3 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MSL3_chrX_11753237_11780772 | MSL3 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | MSL3_chrX_11753237_11780772 | MSL3 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | USA | MSL3_chrX_11753237_11780772 | MSL3 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | MSL3_chrX_11753237_11780772 | MSL3 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | MSL3_chrX_11753237_11780772 | MSL3 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0066 | REF | REF | MSL3_chrX_11753237_11780772 | MSL3 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | MSL3_chrX_11753237_11780772 | MSL3 |
chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:11761518
|
A | G | 1 | a0002 | 2 | HG04184.hp1 HG04199.hp1 |
missense_variant | MODERATE | c.401A>G | p.Asp134Gly | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 5/13 | 428/2286 | 401/1566 | 134/521 | chrX | 11761518 | ||
chrX:11768655
|
A | AG | 1 | a0003 | 1 | HG01168.hp1 | frameshift_variant | HIGH | c.1257dupG | p.Arg420fs | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/13 | 1285/2286 | 1258/1566 | 420/521 | INFO_REALIGN_3_PRIME | chrX | 11768655 | |
chrX:11775025
|
T | A | 1 | a0004 | 1 | NA19006.hp1 | stop_gained | HIGH | c.1512T>A | p.Tyr504* | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 13/13 | 1539/2286 | 1512/1566 | 504/521 | chrX | 11775025 |
chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:11761513
|
C | T | 1 | a0001c0003 | 7 | HG01891.hp1 HG02897.hp1 HG03195.hp1 others(4): Show |
synonymous_variant | LOW | c.396C>T | p.Ser132Ser | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 5/13 | 423/2286 | 396/1566 | 132/521 | chrX | 11761513 | ||
chrX:11762983
|
C | A | 1 | a0001c0005 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.735C>A | p.Ile245Ile | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 7/13 | 762/2286 | 735/1566 | 245/521 | chrX | 11762983 | ||
chrX:11765653
|
C | T | 1 | a0001c0008 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.1095C>T | p.Ser365Ser | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/13 | 1122/2286 | 1095/1566 | 365/521 | chrX | 11765653 | ||
chrX:11775019
|
G | A | 1 | a0001c0002 | 10 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(7): Show |
synonymous_variant | LOW | c.1506G>A | p.Ser502Ser | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 13/13 | 1533/2286 | 1506/1566 | 502/521 | chrX | 11775019 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:11758249
|
C | T | 1 | a0001c0001t0004 | 1 | HG02132.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-15C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/13 | chrX | 11758249 | ||||||
chrX:11775168
|
C | CA | 1 | a0004c0006t0003 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*89_*90insA | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 13/13 | 90 | chrX | 11775168 | |||||
chrX:11775185
|
A | G | 2 | a0001c0001t0002a0001c0001t0004 | 45 | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*106A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 13/13 | 106 | chrX | 11775185 | |||||
chrX:11775250
|
TC | T | 1 | a0004c0006t0003 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*174delC | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 13/13 | 174 | INFO_REALIGN_3_PRIME | chrX | 11775250 | ||||
chrX:11775275
|
A | AC | 1 | a0004c0006t0003 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*197dupC | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 13/13 | 198 | INFO_REALIGN_3_PRIME | chrX | 11775275 | ||||
chrX:11775616
|
A | AT | 1 | a0004c0006t0003 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*542dupT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 13/13 | 543 | INFO_REALIGN_3_PRIME | chrX | 11775616 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:11758401
|
T | TGGGGGAC others(8): Show |
1 | a0001c0001t0001g0017 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.102+42_102+56dupAC others(13): Show |
MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 11758401 | |||||
chrX:11758422
|
C | CG | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.102+62dupG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 11758422 | |||||
chrX:11758428
|
C | CG | 1 | a0001c0001t0002g0093 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.102+68dupG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 11758428 | |||||
chrX:11758443
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.102+78G>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11758443 | ||||||
chrX:11758465
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.102+100G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11758465 | ||||||
chrX:11758742
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.102+377C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11758742 | ||||||
chrX:11758797
|
G | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(10): Show | 28 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.102+432G>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11758797 | ||||||
chrX:11758798
|
C | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(10): Show | 28 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.102+433C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11758798 | ||||||
chrX:11758816
|
C | T | 1 | a0001c0008t0001g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.102+451C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11758816 | ||||||
chrX:11759045
|
A | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 14 | HG01106.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.102+680A>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11759045 | ||||||
chrX:11759172
|
G | A | 3 | a0001c0001t0001g0030a0001c0008t0001g0082a0003c0007t0001g0094 | 3 | HG01168.hp1 HG01169.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.103-621G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11759172 | ||||||
chrX:11759197
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.103-596C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11759197 | ||||||
chrX:11759282
|
G | C | 1 | a0001c0001t0001g0018 | 2 | NA18997.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.103-511G>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11759282 | ||||||
chrX:11759303
|
C | T | 1 | a0001c0001t0001g0026 | 2 | NA18955.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.103-490C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11759303 | ||||||
chrX:11759350
|
A | AG | 10 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 19 | HG01192.hp1 HG01256.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.103-433dupG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 11759350 | |||||
chrX:11759350
|
A | AGG | 2 | a0001c0001t0001g0075a0001c0008t0001g0082 | 2 | HG02280.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.103-434_103-433dup others(2): Show |
MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 11759350 | |||||
chrX:11759350
|
AG | A | 7 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0034others(4): Show | 12 | HG01891.hp2 HG01934.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.103-433delG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 11759350 | |||||
chrX:11759355
|
G | C | 1 | a0001c0001t0001g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.103-438G>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11759355 | ||||||
chrX:11759381
|
A | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(10): Show | 28 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.103-412A>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11759381 | ||||||
chrX:11759629
|
C | CA | 1 | a0001c0001t0001g0084 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.103-163dupA | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 11759629 | |||||
chrX:11759638
|
G | GA | 1 | a0001c0001t0001g0035 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.103-148dupA | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chrX | 11759638 | |||||
chrX:11759666
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.103-127C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11759666 | ||||||
chrX:11759733
|
G | C | 2 | a0001c0001t0001g0014a0001c0001t0001g0036 | 4 | HG02040.hp1 NA18975.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-60G>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 1/12 | chrX | 11759733 | ||||||
chrX:11759900
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.185+25T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 2/12 | chrX | 11759900 | ||||||
chrX:11760183
|
A | C | 1 | a0001c0008t0001g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.186-220A>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 2/12 | chrX | 11760183 | ||||||
chrX:11760352
|
G | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(28): Show | 71 | HG00323.hp1 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.186-51G>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 2/12 | chrX | 11760352 | ||||||
chrX:11760664
|
C | CCTT | 31 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(28): Show | 71 | HG00323.hp1 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.281+166_281+167ins others(3): Show |
MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 3/12 | chrX | 11760664 | ||||||
chrX:11760748
|
A | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0070 | 5 | HG02109.hp2 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.282-89A>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 3/12 | chrX | 11760748 | ||||||
chrX:11761160
|
T | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG02965.hp1 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.382+223T>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 4/12 | chrX | 11761160 | ||||||
chrX:11761399
|
T | G | 1 | a0001c0001t0001g0020 | 2 | HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.383-101T>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 4/12 | chrX | 11761399 | ||||||
chrX:11761419
|
A | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(28): Show | 71 | HG00323.hp1 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.383-81A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 4/12 | chrX | 11761419 | ||||||
chrX:11761436
|
C | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0027 | 9 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.383-64C>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 4/12 | chrX | 11761436 | ||||||
chrX:11761718
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.465+136A>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 5/12 | chrX | 11761718 | ||||||
chrX:11761862
|
C | G | 1 | a0001c0001t0001g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.466-268C>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 5/12 | chrX | 11761862 | ||||||
chrX:11762309
|
G | GT | 1 | a0001c0001t0002g0065 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.588+60dupT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chrX | 11762309 | |||||
chrX:11762317
|
T | G | 1 | a0001c0008t0001g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.588+65T>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 6/12 | chrX | 11762317 | ||||||
chrX:11762326
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.588+74T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 6/12 | chrX | 11762326 | ||||||
chrX:11762351
|
C | T | 1 | a0001c0001t0002g0064 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.588+99C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 6/12 | chrX | 11762351 | ||||||
chrX:11762769
|
T | G | 1 | a0001c0001t0001g0038 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.589-68T>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 6/12 | chrX | 11762769 | ||||||
chrX:11763234
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0002g0065 | 2 | NA19012.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.749+237A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 7/12 | chrX | 11763234 | ||||||
chrX:11763288
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.749+291A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 7/12 | chrX | 11763288 | ||||||
chrX:11763657
|
T | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(28): Show | 71 | HG00323.hp1 HG00735.hp2 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.750-123T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 7/12 | chrX | 11763657 | ||||||
chrX:11763662
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG00735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.750-118G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 7/12 | chrX | 11763662 | ||||||
chrX:11763710
|
A | C | 1 | a0001c0001t0001g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.750-70A>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 7/12 | chrX | 11763710 | ||||||
chrX:11764141
|
C | T | 2 | a0001c0003t0001g0060a0001c0003t0001g0061 | 2 | HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.908+203C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11764141 | ||||||
chrX:11764170
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0002g0065 | 2 | NA19012.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.908+232G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11764170 | ||||||
chrX:11764344
|
C | T | 1 | a0001c0008t0001g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.908+406C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11764344 | ||||||
chrX:11764558
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.908+620C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11764558 | ||||||
chrX:11764718
|
CT | C | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.909-744delT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chrX | 11764718 | |||||
chrX:11764820
|
A | G | 1 | a0001c0008t0001g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.909-647A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11764820 | ||||||
chrX:11764821
|
T | G | 1 | a0001c0001t0001g0039 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.909-646T>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11764821 | ||||||
chrX:11764963
|
T | C | 1 | a0001c0008t0001g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.909-504T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11764963 | ||||||
chrX:11765047
|
T | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(14): Show | 41 | HG00323.hp1 HG01070.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.909-420T>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11765047 | ||||||
chrX:11765107
|
G | C | 1 | a0001c0002t0001g0015 | 3 | HG01109.hp1 HG02109.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.909-360G>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11765107 | ||||||
chrX:11765145
|
A | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(28): Show | 70 | HG00323.hp1 HG00735.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.909-322A>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11765145 | ||||||
chrX:11765172
|
G | C | 9 | a0001c0001t0001g0010a0001c0001t0001g0028a0001c0001t0001g0030others(6): Show | 14 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.909-295G>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11765172 | ||||||
chrX:11765281
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(8): Show | 26 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.909-186A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11765281 | ||||||
chrX:11765284
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.909-183T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11765284 | ||||||
chrX:11765383
|
G | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(13): Show | 40 | HG00323.hp1 HG01070.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.909-84G>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11765383 | ||||||
chrX:11765447
|
A | T | 1 | a0001c0003t0001g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.909-20A>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 8/12 | chrX | 11765447 | ||||||
chrX:11765889
|
A | G | 2 | a0001c0003t0001g0060a0001c0003t0001g0061 | 2 | HG02897.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1171+160A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11765889 | ||||||
chrX:11765918
|
C | T | 1 | a0001c0001t0002g0056 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1171+189C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11765918 | ||||||
chrX:11766018
|
A | G | 1 | a0001c0001t0001g0017 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1171+289A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766018 | ||||||
chrX:11766149
|
A | T | 1 | a0001c0001t0001g0088 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1171+420A>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766149 | ||||||
chrX:11766154
|
CA | C | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1171+428delA | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11766154 | |||||
chrX:11766202
|
GC | G | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1171+476delC | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11766202 | |||||
chrX:11766227
|
T | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(9): Show | 27 | HG00735.hp2 HG01168.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.1171+498T>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766227 | ||||||
chrX:11766287
|
CT | C | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1171+561delT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11766287 | |||||
chrX:11766376
|
C | CA | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1171+652dupA | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11766376 | |||||
chrX:11766516
|
A | T | 1 | a0001c0001t0001g0055 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1171+787A>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766516 | ||||||
chrX:11766566
|
T | C | 1 | a0001c0008t0001g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1171+837T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766566 | ||||||
chrX:11766583
|
AC | A | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1171+857delC | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11766583 | |||||
chrX:11766637
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1171+908G>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766637 | ||||||
chrX:11766669
|
T | C | 1 | a0001c0008t0001g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1171+940T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766669 | ||||||
chrX:11766676
|
G | C | 1 | a0001c0001t0001g0040 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1171+947G>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766676 | ||||||
chrX:11766680
|
G | A | 3 | a0001c0001t0001g0058a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG00735.hp2 HG03239.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1171+951G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766680 | ||||||
chrX:11766733
|
GA | G | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1171+1007delA | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11766733 | |||||
chrX:11766745
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1171+1016C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766745 | ||||||
chrX:11766787
|
G | T | 2 | a0001c0001t0001g0054a0001c0001t0001g0076 | 2 | NA18942.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1171+1058G>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766787 | ||||||
chrX:11766836
|
A | G | 2 | a0001c0001t0001g0034a0001c0002t0001g0019 | 3 | HG01891.hp2 HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1171+1107A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766836 | ||||||
chrX:11766901
|
G | A | 1 | a0001c0003t0001g0060 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1171+1172G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11766901 | ||||||
chrX:11766904
|
T | TC | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1171+1179dupC | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11766904 | |||||
chrX:11767314
|
A | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(6): Show | 24 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.1172-1259A>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11767314 | ||||||
chrX:11767414
|
G | GC | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-1157dupC | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11767414 | |||||
chrX:11767536
|
TG | T | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-1035delG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11767536 | |||||
chrX:11767719
|
AT | A | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-850delT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11767719 | |||||
chrX:11767759
|
A | G | 5 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0081others(2): Show | 13 | HG01106.hp1 HG02257.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1172-814A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11767759 | ||||||
chrX:11767784
|
TC | T | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-785delC | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11767784 | |||||
chrX:11767801
|
A | AG | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-772_1172-771i others(3): Show |
MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11767801 | ||||||
chrX:11767805
|
A | G | 18 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(15): Show | 43 | HG00323.hp1 HG01070.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1172-768A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11767805 | ||||||
chrX:11767805
|
AT | A | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-765delT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11767805 | |||||
chrX:11767817
|
A | T | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-756A>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11767817 | ||||||
chrX:11767819
|
A | AG | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-754_1172-753i others(3): Show |
MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11767819 | ||||||
chrX:11767826
|
A | AG | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-746dupG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11767826 | |||||
chrX:11767918
|
AT | A | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-650delT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11767918 | |||||
chrX:11767967
|
CT | C | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-601delT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11767967 | |||||
chrX:11767994
|
AT | A | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-573delT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11767994 | |||||
chrX:11768150
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0024 | 4 | HG01175.hp2 HG01192.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1172-423C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11768150 | ||||||
chrX:11768186
|
C | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(7): Show | 25 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.1172-387C>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11768186 | ||||||
chrX:11768369
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1172-204C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | chrX | 11768369 | ||||||
chrX:11768489
|
AT | A | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1172-81delT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11768489 | |||||
chrX:11768567
|
TG | T | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | splice_region_variant&intron_variant | LOW | c.1172-4delG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chrX | 11768567 | |||||
chrX:11768720
|
T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(93): Show | 285 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.1281+38T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11768720 | ||||||
chrX:11769311
|
AG | A | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1281+632delG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11769311 | |||||
chrX:11769370
|
G | A | 1 | a0001c0001t0001g0008 | 7 | HG02280.hp2 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1281+688G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11769370 | ||||||
chrX:11769542
|
C | CT | 1 | a0004c0006t0003g0051 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1281+867dupT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11769542 | |||||
chrX:11769571
|
AG | A | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1281+892delG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11769571 | |||||
chrX:11769600
|
A | T | 1 | a0001c0001t0001g0050 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1281+918A>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11769600 | ||||||
chrX:11769621
|
AG | A | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1281+942delG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11769621 | |||||
chrX:11769666
|
G | GA | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1281+984_1281+985i others(3): Show |
MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11769666 | ||||||
chrX:11769799
|
T | A | 1 | a0001c0001t0002g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1281+1117T>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11769799 | ||||||
chrX:11769818
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1281+1136C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11769818 | ||||||
chrX:11769827
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1281+1145A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11769827 | ||||||
chrX:11769850
|
C | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0027others(4): Show | 17 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1281+1168C>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11769850 | ||||||
chrX:11769876
|
G | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0018others(2): Show | 15 | HG00323.hp1 HG01070.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.1281+1194G>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11769876 | ||||||
chrX:11769884
|
G | GC | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1281+1203dupC | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11769884 | |||||
chrX:11769927
|
TG | T | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1281+1248delG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11769927 | |||||
chrX:11769959
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(6): Show | 24 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.1281+1277C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11769959 | ||||||
chrX:11770069
|
AG | A | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1281+1391delG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11770069 | |||||
chrX:11770090
|
GC | G | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1281+1413delC | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11770090 | |||||
chrX:11770139
|
T | G | 1 | a0001c0001t0001g0042 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1281+1457T>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11770139 | ||||||
chrX:11770184
|
A | C | 2 | a0001c0001t0001g0006a0001c0001t0001g0034 | 9 | HG00323.hp1 HG01070.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1281+1502A>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11770184 | ||||||
chrX:11770196
|
T | G | 9 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(6): Show | 24 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.1281+1514T>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11770196 | ||||||
chrX:11770219
|
T | C | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(50): Show | 127 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1281+1537T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11770219 | ||||||
chrX:11770270
|
G | GT | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1281+1590dupT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11770270 | |||||
chrX:11770295
|
T | TA | 1 | a0001c0001t0001g0046 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1281+1614dupA | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11770295 | |||||
chrX:11770389
|
AG | A | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1281+1711delG | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11770389 | |||||
chrX:11770428
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0027others(4): Show | 17 | HG00735.hp2 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1282-1728C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11770428 | ||||||
chrX:11770510
|
TGG | T | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1282-1643_1282-164 others(6): Show |
MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11770510 | |||||
chrX:11770553
|
G | A | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1282-1603G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11770553 | ||||||
chrX:11770554
|
A | T | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1282-1602A>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11770554 | ||||||
chrX:11770556
|
T | C | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1282-1600T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11770556 | ||||||
chrX:11770586
|
GT | G | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1282-1564delT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11770586 | |||||
chrX:11770619
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0028 | 7 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1282-1537A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11770619 | ||||||
chrX:11770641
|
G | T | 1 | a0001c0001t0002g0033 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1282-1515G>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11770641 | ||||||
chrX:11770667
|
TA | T | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1282-1486delA | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11770667 | |||||
chrX:11770708
|
TC | T | 1 | a0003c0007t0001g0094 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1282-1443delC | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11770708 | |||||
chrX:11770962
|
C | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0012others(15): Show | 43 | HG00323.hp1 HG01070.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1282-1194C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11770962 | ||||||
chrX:11771179
|
G | C | 1 | a0001c0001t0001g0017 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1282-977G>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11771179 | ||||||
chrX:11771351
|
C | T | 4 | a0001c0003t0001g0011a0001c0003t0001g0057a0001c0003t0001g0060others(1): Show | 7 | HG01891.hp1 HG02897.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1282-805C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11771351 | ||||||
chrX:11771405
|
GT | G | 1 | a0004c0006t0003g0051 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1282-748delT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chrX | 11771405 | |||||
chrX:11771724
|
C | T | 14 | a0001c0001t0002g0002a0001c0001t0002g0023a0001c0001t0002g0032others(11): Show | 40 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1282-432C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11771724 | ||||||
chrX:11771725
|
G | A | 1 | a0001c0001t0001g0017 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1282-431G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11771725 | ||||||
chrX:11771799
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1282-357T>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11771799 | ||||||
chrX:11771807
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1282-349C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11771807 | ||||||
chrX:11771823
|
C | T | 3 | a0001c0001t0001g0030a0001c0008t0001g0082a0003c0007t0001g0094 | 3 | HG01168.hp1 HG01169.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1282-333C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11771823 | ||||||
chrX:11771833
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1282-323G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11771833 | ||||||
chrX:11771873
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1282-283G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 10/12 | chrX | 11771873 | ||||||
chrX:11772618
|
C | T | 1 | a0001c0001t0002g0045 | 1 | NA20129.hp1 | splice_region_variant&intron_variant | LOW | c.1382-3C>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 11/12 | chrX | 11772618 | ||||||
chrX:11772718
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0028 | 7 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1466+13T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | chrX | 11772718 | ||||||
chrX:11772865
|
G | GT | 1 | a0001c0001t0002g0056 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1466+167dupT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 11772865 | |||||
chrX:11773124
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG02965.hp1 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1466+419G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | chrX | 11773124 | ||||||
chrX:11773394
|
TTAAGGAG others(6): Show |
T | 1 | a0004c0006t0003g0051 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1466+691_1466+703d others(15): Show |
MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 11773394 | |||||
chrX:11773438
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0073 | 2 | NA18951.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1466+733T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | chrX | 11773438 | ||||||
chrX:11773764
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1466+1059G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | chrX | 11773764 | ||||||
chrX:11773877
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1467-1103A>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | chrX | 11773877 | ||||||
chrX:11773883
|
GA | G | 2 | a0001c0001t0001g0030a0003c0007t0001g0094 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1467-1092delA | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 11773883 | |||||
chrX:11774106
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1467-874A>T | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | chrX | 11774106 | ||||||
chrX:11774250
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0028 | 7 | HG02723.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1467-730T>C | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | chrX | 11774250 | ||||||
chrX:11774330
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1467-650T>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | chrX | 11774330 | ||||||
chrX:11774438
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1467-542G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | chrX | 11774438 | ||||||
chrX:11774596
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0039 | 7 | NA18942.hp1 NA18947.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1467-384G>A | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | chrX | 11774596 | ||||||
chrX:11774861
|
A | AT | 1 | a0001c0001t0001g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1467-112dupT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 11774861 | |||||
chrX:11774861
|
AT | A | 1 | a0004c0006t0003g0051 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1467-112delT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 11774861 | |||||
chrX:11774905
|
G | GT | 1 | a0004c0006t0003g0051 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1467-73dupT | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 11774905 | |||||
chrX:11774916
|
A | G | 1 | a0001c0001t0001g0013 | 4 | HG02055.hp1 HG02293.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467-64A>G | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | chrX | 11774916 | ||||||
chrX:11774975
|
TC | T | 1 | a0004c0006t0003g0051 | 1 | NA19006.hp1 | splice_region_variant&intron_variant | LOW | c.1467-3delC | MSL3 | ENSG00000005302.19 | transcript | ENST00000312196.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chrX | 11774975 |