SNP Links for Gene (Select 55349) - SNP

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Select item 14915589731.

rs1491558973 [Homo sapiens]

Variant type:: DEL
Alleles:: AC>- [Show Flanks]
Chromosome:: 3:53816131 (GRCh38)
3:53850158 (GRCh37)
Canonical SPDI:: NC_000003.12:53816130:AC:
Gene:: CHDH (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00051/7 (TOMMO)
HGVS:: NC_000003.12:g.53816131_53816132del, NC_000003.11:g.53850158_53850159del, NG_028042.1:g.35262_35263del, NM_018397.5:c.*1645_*1646del

Select item 14915068322.

rs1491506832 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,AA [Show Flanks]
Chromosome:: 3:53813130 (GRCh38)
3:53847158 (GRCh37)
Canonical SPDI:: NC_000003.12:53813130::A,NC_000003.12:53813130::AA
Gene:: CACNA1D (Varview), CHDH (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
HGVS:: NC_000003.12:g.53813130_53813131insA, NC_000003.12:g.53813130_53813131insAA, NC_000003.11:g.53847157_53847158insA, NC_000003.11:g.53847157_53847158insAA, NG_032999.1:g.323082_323083insA, NG_032999.1:g.323082_323083insAA, NM_000720.4:c.*1724_*1725insA, NM_000720.4:c.*1724_*1725insAA, NM_001128840.3:c.*1724_*1725insA, NM_001128840.3:c.*1724_*1725insAA, NM_001128839.3:c.*1724_*1725insA, NM_001128839.3:c.*1724_*1725insAA, NM_018397.5:c.*4646_*4647insT, NM_018397.5:c.*4646_*4647insTT, XM_005265448.4:c.*1724_*1725insA, XM_005265448.4:c.*1724_*1725insAA, XM_005265448.2:c.*1724_*1725insA, XM_005265448.2:c.*1724_*1725insAA, XM_005265448.1:c.*1724_*1725insA, XM_005265448.1:c.*1724_*1725insAA, XM_011534097.3:c.*1724_*1725insA, XM_011534097.3:c.*1724_*1725insAA, XM_011534097.2:c.*1724_*1725insA, XM_011534097.2:c.*1724_*1725insAA, XM_011534097.1:c.*1724_*1725insA, XM_011534097.1:c.*1724_*1725insAA, XM_011534094.3:c.*1724_*1725insA, XM_011534094.3:c.*1724_*1725insAA, XM_011534094.2:c.*1724_*1725insA, XM_011534094.2:c.*1724_*1725insAA, XM_011534094.1:c.*1724_*1725insA, XM_011534094.1:c.*1724_*1725insAA, XM_011534100.3:c.*1724_*1725insA, XM_011534100.3:c.*1724_*1725insAA, XM_011534100.2:c.*1724_*1725insA, XM_011534100.2:c.*1724_*1725insAA, XM_011534100.1:c.*1724_*1725insA, XM_011534100.1:c.*1724_*1725insAA, XM_011534096.3:c.*1724_*1725insA, XM_011534096.3:c.*1724_*1725insAA, XM_011534096.1:c.*1724_*1725insA, XM_011534096.1:c.*1724_*1725insAA, XM_011534099.3:c.*1724_*1725insA, XM_011534099.3:c.*1724_*1725insAA, XM_011534099.2:c.*1724_*1725insA, XM_011534099.2:c.*1724_*1725insAA, XM_011534099.1:c.*1724_*1725insA, XM_011534099.1:c.*1724_*1725insAA, XM_017007137.2:c.*1724_*1725insA, XM_017007137.2:c.*1724_*1725insAA, XM_017007137.1:c.*1724_*1725insA, XM_017007137.1:c.*1724_*1725insAA, XM_017007138.2:c.*1724_*1725insA, XM_017007138.2:c.*1724_*1725insAA, XM_017007138.1:c.*1724_*1725insA, XM_017007138.1:c.*1724_*1725insAA, XM_017007139.2:c.*1724_*1725insA, XM_017007139.2:c.*1724_*1725insAA, XM_017007139.1:c.*1724_*1725insA, XM_017007139.1:c.*1724_*1725insAA, XM_017007141.2:c.*1724_*1725insA, XM_017007141.2:c.*1724_*1725insAA, XM_017007141.1:c.*1724_*1725insA, XM_017007141.1:c.*1724_*1725insAA, XM_017007140.2:c.*1724_*1725insA, XM_017007140.2:c.*1724_*1725insAA, XM_017007140.1:c.*1724_*1725insA, XM_017007140.1:c.*1724_*1725insAA, XM_017007144.2:c.*1724_*1725insA, XM_017007144.2:c.*1724_*1725insAA, XM_017007143.2:c.*1724_*1725insA, XM_017007143.2:c.*1724_*1725insAA, XM_017007143.1:c.*1724_*1725insA, XM_017007143.1:c.*1724_*1725insAA, XM_017007142.2:c.*1724_*1725insA, XM_017007142.2:c.*1724_*1725insAA, XM_017007142.1:c.*1724_*1725insA, XM_017007142.1:c.*1724_*1725insAA, XM_017007145.2:c.*1724_*1725insA, XM_017007145.2:c.*1724_*1725insAA, XM_017007145.1:c.*1724_*1725insA, XM_017007145.1:c.*1724_*1725insAA, XM_047448871.1:c.*1724_*1725insA, XM_047448871.1:c.*1724_*1725insAA, XM_047448872.1:c.*1724_*1725insA, XM_047448872.1:c.*1724_*1725insAA

Select item 14914696513.

rs1491469651 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AT [Show Flanks]
Chromosome:: 3:53829887 (GRCh38)
3:53863915 (GRCh37)
Canonical SPDI:: NC_000003.12:53829887:T:TAT
Gene:: CHDH (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TAT=0./0 (ALFA)
TA=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.53829888_53829889insAT, NC_000003.11:g.53863915_53863916insAT, NG_028042.1:g.21506_21507insTA

Select item 14913966474.

rs1491396647 has merged into rs1174010295 [Homo sapiens]

Variant type:: DELINS
Alleles:: CCC>-,C,CC,CCCC,CCCCC [Show Flanks]
Chromosome:: 3:53843183 (GRCh38)
3:53877210 (GRCh37)
Canonical SPDI:: NC_000003.12:53843177:CCCCCCCC:CCCCC,NC_000003.12:53843177:CCCCCCCC:CCCCCC,NC_000003.12:53843177:CCCCCCCC:CCCCCCC,NC_000003.12:53843177:CCCCCCCC:CCCCCCCCC,NC_000003.12:53843177:CCCCCCCC:CCCCCCCCCC
Gene:: CHDH (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCCCCCC=0./0 (ALFA)
C=0.00047/2 (Estonian)
HGVS:: NC_000003.12:g.53843183_53843185del, NC_000003.12:g.53843184_53843185del, NC_000003.12:g.53843185del, NC_000003.12:g.53843185dup, NC_000003.12:g.53843184_53843185dup, NC_000003.11:g.53877210_53877212del, NC_000003.11:g.53877211_53877212del, NC_000003.11:g.53877212del, NC_000003.11:g.53877212dup, NC_000003.11:g.53877211_53877212dup, NG_028042.1:g.8214_8216del, NG_028042.1:g.8215_8216del, NG_028042.1:g.8216del, NG_028042.1:g.8216dup, NG_028042.1:g.8215_8216dup

Select item 14913661605.

rs1491366160 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 3:53843177 (GRCh38)
3:53877204 (GRCh37)
Canonical SPDI:: NC_000003.12:53843176:TC:
Gene:: CHDH (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00017/2 (ALFA)
HGVS:: NC_000003.12:g.53843177_53843178del, NC_000003.11:g.53877204_53877205del, NG_028042.1:g.8216_8217del

Select item 14912754526.

rs1491275452 has merged into rs59630779 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 3:53813142 (GRCh38)
3:53847169 (GRCh37)
Canonical SPDI:: NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:53813129:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CACNA1D (Varview), CHDH (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
TTT=0.13/651 (1000Genomes)
HGVS:: NC_000003.12:g.53813142_53813152del, NC_000003.12:g.53813143_53813152del, NC_000003.12:g.53813144_53813152del, NC_000003.12:g.53813145_53813152del, NC_000003.12:g.53813146_53813152del, NC_000003.12:g.53813147_53813152del, NC_000003.12:g.53813148_53813152del, NC_000003.12:g.53813149_53813152del, NC_000003.12:g.53813150_53813152del, NC_000003.12:g.53813151_53813152del, NC_000003.12:g.53813152del, NC_000003.12:g.53813152dup, NC_000003.12:g.53813151_53813152dup, NC_000003.12:g.53813150_53813152dup, NC_000003.12:g.53813148_53813152dup, NC_000003.12:g.53813130_53813152T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.12:g.53813152_53813153insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.12:g.53813152_53813153insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.53847169_53847179del, NC_000003.11:g.53847170_53847179del, NC_000003.11:g.53847171_53847179del, NC_000003.11:g.53847172_53847179del, NC_000003.11:g.53847173_53847179del, NC_000003.11:g.53847174_53847179del, NC_000003.11:g.53847175_53847179del, NC_000003.11:g.53847176_53847179del, NC_000003.11:g.53847177_53847179del, NC_000003.11:g.53847178_53847179del, NC_000003.11:g.53847179del, NC_000003.11:g.53847179dup, NC_000003.11:g.53847178_53847179dup, NC_000003.11:g.53847177_53847179dup, NC_000003.11:g.53847175_53847179dup, NC_000003.11:g.53847157_53847179T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000003.11:g.53847179_53847180insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000003.11:g.53847179_53847180insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032999.1:g.323094_323104del, NG_032999.1:g.323095_323104del, NG_032999.1:g.323096_323104del, NG_032999.1:g.323097_323104del, NG_032999.1:g.323098_323104del, NG_032999.1:g.323099_323104del, NG_032999.1:g.323100_323104del, NG_032999.1:g.323101_323104del, NG_032999.1:g.323102_323104del, NG_032999.1:g.323103_323104del, NG_032999.1:g.323104del, NG_032999.1:g.323104dup, NG_032999.1:g.323103_323104dup, NG_032999.1:g.323102_323104dup, NG_032999.1:g.323100_323104dup, NG_032999.1:g.323082_323104T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_032999.1:g.323104_323105insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_032999.1:g.323104_323105insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_000720.4:c.*1736_*1746del, NM_000720.4:c.*1737_*1746del, NM_000720.4:c.*1738_*1746del, NM_000720.4:c.*1739_*1746del, NM_000720.4:c.*1740_*1746del, NM_000720.4:c.*1741_*1746del, NM_000720.4:c.*1742_*1746del, NM_000720.4:c.*1743_*1746del, NM_000720.4:c.*1744_*1746del, NM_000720.4:c.*1745_*1746del, NM_000720.4:c.*1746del, NM_000720.4:c.*1746dup, NM_000720.4:c.*1745_*1746dup, NM_000720.4:c.*1744_*1746dup, NM_000720.4:c.*1742_*1746dup, NM_000720.4:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NM_000720.4:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_000720.4:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001128840.3:c.*1736_*1746del, NM_001128840.3:c.*1737_*1746del, NM_001128840.3:c.*1738_*1746del, NM_001128840.3:c.*1739_*1746del, NM_001128840.3:c.*1740_*1746del, NM_001128840.3:c.*1741_*1746del, NM_001128840.3:c.*1742_*1746del, NM_001128840.3:c.*1743_*1746del, NM_001128840.3:c.*1744_*1746del, NM_001128840.3:c.*1745_*1746del, NM_001128840.3:c.*1746del, NM_001128840.3:c.*1746dup, NM_001128840.3:c.*1745_*1746dup, NM_001128840.3:c.*1744_*1746dup, NM_001128840.3:c.*1742_*1746dup, NM_001128840.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NM_001128840.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001128840.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001128839.3:c.*1736_*1746del, NM_001128839.3:c.*1737_*1746del, NM_001128839.3:c.*1738_*1746del, NM_001128839.3:c.*1739_*1746del, NM_001128839.3:c.*1740_*1746del, NM_001128839.3:c.*1741_*1746del, NM_001128839.3:c.*1742_*1746del, NM_001128839.3:c.*1743_*1746del, NM_001128839.3:c.*1744_*1746del, NM_001128839.3:c.*1745_*1746del, NM_001128839.3:c.*1746del, NM_001128839.3:c.*1746dup, NM_001128839.3:c.*1745_*1746dup, NM_001128839.3:c.*1744_*1746dup, NM_001128839.3:c.*1742_*1746dup, NM_001128839.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], NM_001128839.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001128839.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_018397.5:c.*4637_*4647del, NM_018397.5:c.*4638_*4647del, NM_018397.5:c.*4639_*4647del, NM_018397.5:c.*4640_*4647del, NM_018397.5:c.*4641_*4647del, NM_018397.5:c.*4642_*4647del, NM_018397.5:c.*4643_*4647del, NM_018397.5:c.*4644_*4647del, NM_018397.5:c.*4645_*4647del, NM_018397.5:c.*4646_*4647del, NM_018397.5:c.*4647del, NM_018397.5:c.*4647dup, NM_018397.5:c.*4646_*4647dup, NM_018397.5:c.*4645_*4647dup, NM_018397.5:c.*4643_*4647dup, NM_018397.5:c.*4625_*4647A[25]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NM_018397.5:c.*4647_*4648insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NM_018397.5:c.*4647_*4648insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, XM_005265448.4:c.*1736_*1746del, XM_005265448.4:c.*1737_*1746del, XM_005265448.4:c.*1738_*1746del, XM_005265448.4:c.*1739_*1746del, XM_005265448.4:c.*1740_*1746del, XM_005265448.4:c.*1741_*1746del, XM_005265448.4:c.*1742_*1746del, XM_005265448.4:c.*1743_*1746del, XM_005265448.4:c.*1744_*1746del, XM_005265448.4:c.*1745_*1746del, XM_005265448.4:c.*1746del, XM_005265448.4:c.*1746dup, XM_005265448.4:c.*1745_*1746dup, XM_005265448.4:c.*1744_*1746dup, XM_005265448.4:c.*1742_*1746dup, XM_005265448.4:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_005265448.4:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_005265448.4:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_005265448.2:c.*1745dup, XM_005265448.2:c.*1736_*1745del, XM_005265448.2:c.*1737_*1745del, XM_005265448.2:c.*1738_*1745del, XM_005265448.2:c.*1739_*1745del, XM_005265448.2:c.*1740_*1745del, XM_005265448.2:c.*1741_*1745del, XM_005265448.2:c.*1742_*1745del, XM_005265448.2:c.*1743_*1745del, XM_005265448.2:c.*1744_*1745del, XM_005265448.2:c.*1745del, XM_005265448.2:c.*1744_*1745dup, XM_005265448.2:c.*1743_*1745dup, XM_005265448.2:c.*1742_*1745dup, XM_005265448.2:c.*1740_*1745dup, XM_005265448.2:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_005265448.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_005265448.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_005265448.1:c.*1736_*1746del, XM_005265448.1:c.*1737_*1746del, XM_005265448.1:c.*1738_*1746del, XM_005265448.1:c.*1739_*1746del, XM_005265448.1:c.*1740_*1746del, XM_005265448.1:c.*1741_*1746del, XM_005265448.1:c.*1742_*1746del, XM_005265448.1:c.*1743_*1746del, XM_005265448.1:c.*1744_*1746del, XM_005265448.1:c.*1745_*1746del, XM_005265448.1:c.*1746del, XM_005265448.1:c.*1746dup, XM_005265448.1:c.*1745_*1746dup, XM_005265448.1:c.*1744_*1746dup, XM_005265448.1:c.*1742_*1746dup, XM_005265448.1:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_005265448.1:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_005265448.1:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534097.3:c.*1736_*1746del, XM_011534097.3:c.*1737_*1746del, XM_011534097.3:c.*1738_*1746del, XM_011534097.3:c.*1739_*1746del, XM_011534097.3:c.*1740_*1746del, XM_011534097.3:c.*1741_*1746del, XM_011534097.3:c.*1742_*1746del, XM_011534097.3:c.*1743_*1746del, XM_011534097.3:c.*1744_*1746del, XM_011534097.3:c.*1745_*1746del, XM_011534097.3:c.*1746del, XM_011534097.3:c.*1746dup, XM_011534097.3:c.*1745_*1746dup, XM_011534097.3:c.*1744_*1746dup, XM_011534097.3:c.*1742_*1746dup, XM_011534097.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534097.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534097.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534097.2:c.*1745dup, XM_011534097.2:c.*1736_*1745del, XM_011534097.2:c.*1737_*1745del, XM_011534097.2:c.*1738_*1745del, XM_011534097.2:c.*1739_*1745del, XM_011534097.2:c.*1740_*1745del, XM_011534097.2:c.*1741_*1745del, XM_011534097.2:c.*1742_*1745del, XM_011534097.2:c.*1743_*1745del, XM_011534097.2:c.*1744_*1745del, XM_011534097.2:c.*1745del, XM_011534097.2:c.*1744_*1745dup, XM_011534097.2:c.*1743_*1745dup, XM_011534097.2:c.*1742_*1745dup, XM_011534097.2:c.*1740_*1745dup, XM_011534097.2:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534097.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534097.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534097.1:c.*1745dup, XM_011534097.1:c.*1736_*1745del, XM_011534097.1:c.*1737_*1745del, XM_011534097.1:c.*1738_*1745del, XM_011534097.1:c.*1739_*1745del, XM_011534097.1:c.*1740_*1745del, XM_011534097.1:c.*1741_*1745del, XM_011534097.1:c.*1742_*1745del, XM_011534097.1:c.*1743_*1745del, XM_011534097.1:c.*1744_*1745del, XM_011534097.1:c.*1745del, XM_011534097.1:c.*1744_*1745dup, XM_011534097.1:c.*1743_*1745dup, XM_011534097.1:c.*1742_*1745dup, XM_011534097.1:c.*1740_*1745dup, XM_011534097.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534097.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534097.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534094.3:c.*1736_*1746del, XM_011534094.3:c.*1737_*1746del, XM_011534094.3:c.*1738_*1746del, XM_011534094.3:c.*1739_*1746del, XM_011534094.3:c.*1740_*1746del, XM_011534094.3:c.*1741_*1746del, XM_011534094.3:c.*1742_*1746del, XM_011534094.3:c.*1743_*1746del, XM_011534094.3:c.*1744_*1746del, XM_011534094.3:c.*1745_*1746del, XM_011534094.3:c.*1746del, XM_011534094.3:c.*1746dup, XM_011534094.3:c.*1745_*1746dup, XM_011534094.3:c.*1744_*1746dup, XM_011534094.3:c.*1742_*1746dup, XM_011534094.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534094.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534094.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534094.2:c.*1745dup, XM_011534094.2:c.*1736_*1745del, XM_011534094.2:c.*1737_*1745del, XM_011534094.2:c.*1738_*1745del, XM_011534094.2:c.*1739_*1745del, XM_011534094.2:c.*1740_*1745del, XM_011534094.2:c.*1741_*1745del, XM_011534094.2:c.*1742_*1745del, XM_011534094.2:c.*1743_*1745del, XM_011534094.2:c.*1744_*1745del, XM_011534094.2:c.*1745del, XM_011534094.2:c.*1744_*1745dup, XM_011534094.2:c.*1743_*1745dup, XM_011534094.2:c.*1742_*1745dup, XM_011534094.2:c.*1740_*1745dup, XM_011534094.2:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534094.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534094.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534094.1:c.*1745dup, XM_011534094.1:c.*1736_*1745del, XM_011534094.1:c.*1737_*1745del, XM_011534094.1:c.*1738_*1745del, XM_011534094.1:c.*1739_*1745del, XM_011534094.1:c.*1740_*1745del, XM_011534094.1:c.*1741_*1745del, XM_011534094.1:c.*1742_*1745del, XM_011534094.1:c.*1743_*1745del, XM_011534094.1:c.*1744_*1745del, XM_011534094.1:c.*1745del, XM_011534094.1:c.*1744_*1745dup, XM_011534094.1:c.*1743_*1745dup, XM_011534094.1:c.*1742_*1745dup, XM_011534094.1:c.*1740_*1745dup, XM_011534094.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534094.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534094.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534100.3:c.*1736_*1746del, XM_011534100.3:c.*1737_*1746del, XM_011534100.3:c.*1738_*1746del, XM_011534100.3:c.*1739_*1746del, XM_011534100.3:c.*1740_*1746del, XM_011534100.3:c.*1741_*1746del, XM_011534100.3:c.*1742_*1746del, XM_011534100.3:c.*1743_*1746del, XM_011534100.3:c.*1744_*1746del, XM_011534100.3:c.*1745_*1746del, XM_011534100.3:c.*1746del, XM_011534100.3:c.*1746dup, XM_011534100.3:c.*1745_*1746dup, XM_011534100.3:c.*1744_*1746dup, XM_011534100.3:c.*1742_*1746dup, XM_011534100.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534100.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534100.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534100.2:c.*1745dup, XM_011534100.2:c.*1736_*1745del, XM_011534100.2:c.*1737_*1745del, XM_011534100.2:c.*1738_*1745del, XM_011534100.2:c.*1739_*1745del, XM_011534100.2:c.*1740_*1745del, XM_011534100.2:c.*1741_*1745del, XM_011534100.2:c.*1742_*1745del, XM_011534100.2:c.*1743_*1745del, XM_011534100.2:c.*1744_*1745del, XM_011534100.2:c.*1745del, XM_011534100.2:c.*1744_*1745dup, XM_011534100.2:c.*1743_*1745dup, XM_011534100.2:c.*1742_*1745dup, XM_011534100.2:c.*1740_*1745dup, XM_011534100.2:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534100.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534100.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534100.1:c.*1745dup, XM_011534100.1:c.*1736_*1745del, XM_011534100.1:c.*1737_*1745del, XM_011534100.1:c.*1738_*1745del, XM_011534100.1:c.*1739_*1745del, XM_011534100.1:c.*1740_*1745del, XM_011534100.1:c.*1741_*1745del, XM_011534100.1:c.*1742_*1745del, XM_011534100.1:c.*1743_*1745del, XM_011534100.1:c.*1744_*1745del, XM_011534100.1:c.*1745del, XM_011534100.1:c.*1744_*1745dup, XM_011534100.1:c.*1743_*1745dup, XM_011534100.1:c.*1742_*1745dup, XM_011534100.1:c.*1740_*1745dup, XM_011534100.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534100.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534100.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534096.3:c.*1736_*1746del, XM_011534096.3:c.*1737_*1746del, XM_011534096.3:c.*1738_*1746del, XM_011534096.3:c.*1739_*1746del, XM_011534096.3:c.*1740_*1746del, XM_011534096.3:c.*1741_*1746del, XM_011534096.3:c.*1742_*1746del, XM_011534096.3:c.*1743_*1746del, XM_011534096.3:c.*1744_*1746del, XM_011534096.3:c.*1745_*1746del, XM_011534096.3:c.*1746del, XM_011534096.3:c.*1746dup, XM_011534096.3:c.*1745_*1746dup, XM_011534096.3:c.*1744_*1746dup, XM_011534096.3:c.*1742_*1746dup, XM_011534096.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534096.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534096.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534096.1:c.*1745dup, XM_011534096.1:c.*1736_*1745del, XM_011534096.1:c.*1737_*1745del, XM_011534096.1:c.*1738_*1745del, XM_011534096.1:c.*1739_*1745del, XM_011534096.1:c.*1740_*1745del, XM_011534096.1:c.*1741_*1745del, XM_011534096.1:c.*1742_*1745del, XM_011534096.1:c.*1743_*1745del, XM_011534096.1:c.*1744_*1745del, XM_011534096.1:c.*1745del, XM_011534096.1:c.*1744_*1745dup, XM_011534096.1:c.*1743_*1745dup, XM_011534096.1:c.*1742_*1745dup, XM_011534096.1:c.*1740_*1745dup, XM_011534096.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534096.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534096.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534099.3:c.*1736_*1746del, XM_011534099.3:c.*1737_*1746del, XM_011534099.3:c.*1738_*1746del, XM_011534099.3:c.*1739_*1746del, XM_011534099.3:c.*1740_*1746del, XM_011534099.3:c.*1741_*1746del, XM_011534099.3:c.*1742_*1746del, XM_011534099.3:c.*1743_*1746del, XM_011534099.3:c.*1744_*1746del, XM_011534099.3:c.*1745_*1746del, XM_011534099.3:c.*1746del, XM_011534099.3:c.*1746dup, XM_011534099.3:c.*1745_*1746dup, XM_011534099.3:c.*1744_*1746dup, XM_011534099.3:c.*1742_*1746dup, XM_011534099.3:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534099.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534099.3:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534099.2:c.*1745dup, XM_011534099.2:c.*1736_*1745del, XM_011534099.2:c.*1737_*1745del, XM_011534099.2:c.*1738_*1745del, XM_011534099.2:c.*1739_*1745del, XM_011534099.2:c.*1740_*1745del, XM_011534099.2:c.*1741_*1745del, XM_011534099.2:c.*1742_*1745del, XM_011534099.2:c.*1743_*1745del, XM_011534099.2:c.*1744_*1745del, XM_011534099.2:c.*1745del, XM_011534099.2:c.*1744_*1745dup, XM_011534099.2:c.*1743_*1745dup, XM_011534099.2:c.*1742_*1745dup, XM_011534099.2:c.*1740_*1745dup, XM_011534099.2:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534099.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534099.2:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534099.1:c.*1745dup, XM_011534099.1:c.*1736_*1745del, XM_011534099.1:c.*1737_*1745del, XM_011534099.1:c.*1738_*1745del, XM_011534099.1:c.*1739_*1745del, XM_011534099.1:c.*1740_*1745del, XM_011534099.1:c.*1741_*1745del, XM_011534099.1:c.*1742_*1745del, XM_011534099.1:c.*1743_*1745del, XM_011534099.1:c.*1744_*1745del, XM_011534099.1:c.*1745del, XM_011534099.1:c.*1744_*1745dup, XM_011534099.1:c.*1743_*1745dup, XM_011534099.1:c.*1742_*1745dup, XM_011534099.1:c.*1740_*1745dup, XM_011534099.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_011534099.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011534099.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007137.2:c.*1736_*1746del, XM_017007137.2:c.*1737_*1746del, XM_017007137.2:c.*1738_*1746del, XM_017007137.2:c.*1739_*1746del, XM_017007137.2:c.*1740_*1746del, XM_017007137.2:c.*1741_*1746del, XM_017007137.2:c.*1742_*1746del, XM_017007137.2:c.*1743_*1746del, XM_017007137.2:c.*1744_*1746del, XM_017007137.2:c.*1745_*1746del, XM_017007137.2:c.*1746del, XM_017007137.2:c.*1746dup, XM_017007137.2:c.*1745_*1746dup, XM_017007137.2:c.*1744_*1746dup, XM_017007137.2:c.*1742_*1746dup, XM_017007137.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007137.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007137.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007137.1:c.*1745dup, XM_017007137.1:c.*1736_*1745del, XM_017007137.1:c.*1737_*1745del, XM_017007137.1:c.*1738_*1745del, XM_017007137.1:c.*1739_*1745del, XM_017007137.1:c.*1740_*1745del, XM_017007137.1:c.*1741_*1745del, XM_017007137.1:c.*1742_*1745del, XM_017007137.1:c.*1743_*1745del, XM_017007137.1:c.*1744_*1745del, XM_017007137.1:c.*1745del, XM_017007137.1:c.*1744_*1745dup, XM_017007137.1:c.*1743_*1745dup, XM_017007137.1:c.*1742_*1745dup, XM_017007137.1:c.*1740_*1745dup, XM_017007137.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007137.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007137.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007138.2:c.*1736_*1746del, XM_017007138.2:c.*1737_*1746del, XM_017007138.2:c.*1738_*1746del, XM_017007138.2:c.*1739_*1746del, XM_017007138.2:c.*1740_*1746del, XM_017007138.2:c.*1741_*1746del, XM_017007138.2:c.*1742_*1746del, XM_017007138.2:c.*1743_*1746del, XM_017007138.2:c.*1744_*1746del, XM_017007138.2:c.*1745_*1746del, XM_017007138.2:c.*1746del, XM_017007138.2:c.*1746dup, XM_017007138.2:c.*1745_*1746dup, XM_017007138.2:c.*1744_*1746dup, XM_017007138.2:c.*1742_*1746dup, XM_017007138.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007138.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007138.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007138.1:c.*1745dup, XM_017007138.1:c.*1736_*1745del, XM_017007138.1:c.*1737_*1745del, XM_017007138.1:c.*1738_*1745del, XM_017007138.1:c.*1739_*1745del, XM_017007138.1:c.*1740_*1745del, XM_017007138.1:c.*1741_*1745del, XM_017007138.1:c.*1742_*1745del, XM_017007138.1:c.*1743_*1745del, XM_017007138.1:c.*1744_*1745del, XM_017007138.1:c.*1745del, XM_017007138.1:c.*1744_*1745dup, XM_017007138.1:c.*1743_*1745dup, XM_017007138.1:c.*1742_*1745dup, XM_017007138.1:c.*1740_*1745dup, XM_017007138.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007138.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007138.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007139.2:c.*1736_*1746del, XM_017007139.2:c.*1737_*1746del, XM_017007139.2:c.*1738_*1746del, XM_017007139.2:c.*1739_*1746del, XM_017007139.2:c.*1740_*1746del, XM_017007139.2:c.*1741_*1746del, XM_017007139.2:c.*1742_*1746del, XM_017007139.2:c.*1743_*1746del, XM_017007139.2:c.*1744_*1746del, XM_017007139.2:c.*1745_*1746del, XM_017007139.2:c.*1746del, XM_017007139.2:c.*1746dup, XM_017007139.2:c.*1745_*1746dup, XM_017007139.2:c.*1744_*1746dup, XM_017007139.2:c.*1742_*1746dup, XM_017007139.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007139.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007139.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007139.1:c.*1745dup, XM_017007139.1:c.*1736_*1745del, XM_017007139.1:c.*1737_*1745del, XM_017007139.1:c.*1738_*1745del, XM_017007139.1:c.*1739_*1745del, XM_017007139.1:c.*1740_*1745del, XM_017007139.1:c.*1741_*1745del, XM_017007139.1:c.*1742_*1745del, XM_017007139.1:c.*1743_*1745del, XM_017007139.1:c.*1744_*1745del, XM_017007139.1:c.*1745del, XM_017007139.1:c.*1744_*1745dup, XM_017007139.1:c.*1743_*1745dup, XM_017007139.1:c.*1742_*1745dup, XM_017007139.1:c.*1740_*1745dup, XM_017007139.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007139.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007139.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007141.2:c.*1736_*1746del, XM_017007141.2:c.*1737_*1746del, XM_017007141.2:c.*1738_*1746del, XM_017007141.2:c.*1739_*1746del, XM_017007141.2:c.*1740_*1746del, XM_017007141.2:c.*1741_*1746del, XM_017007141.2:c.*1742_*1746del, XM_017007141.2:c.*1743_*1746del, XM_017007141.2:c.*1744_*1746del, XM_017007141.2:c.*1745_*1746del, XM_017007141.2:c.*1746del, XM_017007141.2:c.*1746dup, XM_017007141.2:c.*1745_*1746dup, XM_017007141.2:c.*1744_*1746dup, XM_017007141.2:c.*1742_*1746dup, XM_017007141.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007141.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007141.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007141.1:c.*1745dup, XM_017007141.1:c.*1736_*1745del, XM_017007141.1:c.*1737_*1745del, XM_017007141.1:c.*1738_*1745del, XM_017007141.1:c.*1739_*1745del, XM_017007141.1:c.*1740_*1745del, XM_017007141.1:c.*1741_*1745del, XM_017007141.1:c.*1742_*1745del, XM_017007141.1:c.*1743_*1745del, XM_017007141.1:c.*1744_*1745del, XM_017007141.1:c.*1745del, XM_017007141.1:c.*1744_*1745dup, XM_017007141.1:c.*1743_*1745dup, XM_017007141.1:c.*1742_*1745dup, XM_017007141.1:c.*1740_*1745dup, XM_017007141.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007141.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007141.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007140.2:c.*1736_*1746del, XM_017007140.2:c.*1737_*1746del, XM_017007140.2:c.*1738_*1746del, XM_017007140.2:c.*1739_*1746del, XM_017007140.2:c.*1740_*1746del, XM_017007140.2:c.*1741_*1746del, XM_017007140.2:c.*1742_*1746del, XM_017007140.2:c.*1743_*1746del, XM_017007140.2:c.*1744_*1746del, XM_017007140.2:c.*1745_*1746del, XM_017007140.2:c.*1746del, XM_017007140.2:c.*1746dup, XM_017007140.2:c.*1745_*1746dup, XM_017007140.2:c.*1744_*1746dup, XM_017007140.2:c.*1742_*1746dup, XM_017007140.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007140.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007140.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007140.1:c.*1745dup, XM_017007140.1:c.*1736_*1745del, XM_017007140.1:c.*1737_*1745del, XM_017007140.1:c.*1738_*1745del, XM_017007140.1:c.*1739_*1745del, XM_017007140.1:c.*1740_*1745del, XM_017007140.1:c.*1741_*1745del, XM_017007140.1:c.*1742_*1745del, XM_017007140.1:c.*1743_*1745del, XM_017007140.1:c.*1744_*1745del, XM_017007140.1:c.*1745del, XM_017007140.1:c.*1744_*1745dup, XM_017007140.1:c.*1743_*1745dup, XM_017007140.1:c.*1742_*1745dup, XM_017007140.1:c.*1740_*1745dup, XM_017007140.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007140.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007140.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007144.2:c.*1736_*1746del, XM_017007144.2:c.*1737_*1746del, XM_017007144.2:c.*1738_*1746del, XM_017007144.2:c.*1739_*1746del, XM_017007144.2:c.*1740_*1746del, XM_017007144.2:c.*1741_*1746del, XM_017007144.2:c.*1742_*1746del, XM_017007144.2:c.*1743_*1746del, XM_017007144.2:c.*1744_*1746del, XM_017007144.2:c.*1745_*1746del, XM_017007144.2:c.*1746del, XM_017007144.2:c.*1746dup, XM_017007144.2:c.*1745_*1746dup, XM_017007144.2:c.*1744_*1746dup, XM_017007144.2:c.*1742_*1746dup, XM_017007144.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007144.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007144.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007143.2:c.*1736_*1746del, XM_017007143.2:c.*1737_*1746del, XM_017007143.2:c.*1738_*1746del, XM_017007143.2:c.*1739_*1746del, XM_017007143.2:c.*1740_*1746del, XM_017007143.2:c.*1741_*1746del, XM_017007143.2:c.*1742_*1746del, XM_017007143.2:c.*1743_*1746del, XM_017007143.2:c.*1744_*1746del, XM_017007143.2:c.*1745_*1746del, XM_017007143.2:c.*1746del, XM_017007143.2:c.*1746dup, XM_017007143.2:c.*1745_*1746dup, XM_017007143.2:c.*1744_*1746dup, XM_017007143.2:c.*1742_*1746dup, XM_017007143.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007143.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007143.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007143.1:c.*1745dup, XM_017007143.1:c.*1736_*1745del, XM_017007143.1:c.*1737_*1745del, XM_017007143.1:c.*1738_*1745del, XM_017007143.1:c.*1739_*1745del, XM_017007143.1:c.*1740_*1745del, XM_017007143.1:c.*1741_*1745del, XM_017007143.1:c.*1742_*1745del, XM_017007143.1:c.*1743_*1745del, XM_017007143.1:c.*1744_*1745del, XM_017007143.1:c.*1745del, XM_017007143.1:c.*1744_*1745dup, XM_017007143.1:c.*1743_*1745dup, XM_017007143.1:c.*1742_*1745dup, XM_017007143.1:c.*1740_*1745dup, XM_017007143.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007143.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007143.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007142.2:c.*1736_*1746del, XM_017007142.2:c.*1737_*1746del, XM_017007142.2:c.*1738_*1746del, XM_017007142.2:c.*1739_*1746del, XM_017007142.2:c.*1740_*1746del, XM_017007142.2:c.*1741_*1746del, XM_017007142.2:c.*1742_*1746del, XM_017007142.2:c.*1743_*1746del, XM_017007142.2:c.*1744_*1746del, XM_017007142.2:c.*1745_*1746del, XM_017007142.2:c.*1746del, XM_017007142.2:c.*1746dup, XM_017007142.2:c.*1745_*1746dup, XM_017007142.2:c.*1744_*1746dup, XM_017007142.2:c.*1742_*1746dup, XM_017007142.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007142.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007142.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007142.1:c.*1745dup, XM_017007142.1:c.*1736_*1745del, XM_017007142.1:c.*1737_*1745del, XM_017007142.1:c.*1738_*1745del, XM_017007142.1:c.*1739_*1745del, XM_017007142.1:c.*1740_*1745del, XM_017007142.1:c.*1741_*1745del, XM_017007142.1:c.*1742_*1745del, XM_017007142.1:c.*1743_*1745del, XM_017007142.1:c.*1744_*1745del, XM_017007142.1:c.*1745del, XM_017007142.1:c.*1744_*1745dup, XM_017007142.1:c.*1743_*1745dup, XM_017007142.1:c.*1742_*1745dup, XM_017007142.1:c.*1740_*1745dup, XM_017007142.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007142.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007142.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007145.2:c.*1736_*1746del, XM_017007145.2:c.*1737_*1746del, XM_017007145.2:c.*1738_*1746del, XM_017007145.2:c.*1739_*1746del, XM_017007145.2:c.*1740_*1746del, XM_017007145.2:c.*1741_*1746del, XM_017007145.2:c.*1742_*1746del, XM_017007145.2:c.*1743_*1746del, XM_017007145.2:c.*1744_*1746del, XM_017007145.2:c.*1745_*1746del, XM_017007145.2:c.*1746del, XM_017007145.2:c.*1746dup, XM_017007145.2:c.*1745_*1746dup, XM_017007145.2:c.*1744_*1746dup, XM_017007145.2:c.*1742_*1746dup, XM_017007145.2:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007145.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007145.2:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007145.1:c.*1745dup, XM_017007145.1:c.*1736_*1745del, XM_017007145.1:c.*1737_*1745del, XM_017007145.1:c.*1738_*1745del, XM_017007145.1:c.*1739_*1745del, XM_017007145.1:c.*1740_*1745del, XM_017007145.1:c.*1741_*1745del, XM_017007145.1:c.*1742_*1745del, XM_017007145.1:c.*1743_*1745del, XM_017007145.1:c.*1744_*1745del, XM_017007145.1:c.*1745del, XM_017007145.1:c.*1744_*1745dup, XM_017007145.1:c.*1743_*1745dup, XM_017007145.1:c.*1742_*1745dup, XM_017007145.1:c.*1740_*1745dup, XM_017007145.1:c.*1724_*1745T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_017007145.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017007145.1:c.*1745_*1746insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047448871.1:c.*1736_*1746del, XM_047448871.1:c.*1737_*1746del, XM_047448871.1:c.*1738_*1746del, XM_047448871.1:c.*1739_*1746del, XM_047448871.1:c.*1740_*1746del, XM_047448871.1:c.*1741_*1746del, XM_047448871.1:c.*1742_*1746del, XM_047448871.1:c.*1743_*1746del, XM_047448871.1:c.*1744_*1746del, XM_047448871.1:c.*1745_*1746del, XM_047448871.1:c.*1746del, XM_047448871.1:c.*1746dup, XM_047448871.1:c.*1745_*1746dup, XM_047448871.1:c.*1744_*1746dup, XM_047448871.1:c.*1742_*1746dup, XM_047448871.1:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_047448871.1:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047448871.1:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047448872.1:c.*1736_*1746del, XM_047448872.1:c.*1737_*1746del, XM_047448872.1:c.*1738_*1746del, XM_047448872.1:c.*1739_*1746del, XM_047448872.1:c.*1740_*1746del, XM_047448872.1:c.*1741_*1746del, XM_047448872.1:c.*1742_*1746del, XM_047448872.1:c.*1743_*1746del, XM_047448872.1:c.*1744_*1746del, XM_047448872.1:c.*1745_*1746del, XM_047448872.1:c.*1746del, XM_047448872.1:c.*1746dup, XM_047448872.1:c.*1745_*1746dup, XM_047448872.1:c.*1744_*1746dup, XM_047448872.1:c.*1742_*1746dup, XM_047448872.1:c.*1724_*1746T[31]ATTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_047448872.1:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047448872.1:c.*1746_*1747insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14910802467.

rs1491080246 has merged into rs34884918 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATATAT>-,AT,ATAT,ATATATAT,ATATATATAT,ATATATATATAT,ATATATATATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT,ATATATATATATATATATATAT,ATATATATATATATATATATATAT,ATATATATATATATATATATATATAT [Show Flanks]
Chromosome:: 3:53830416 (GRCh38)
3:53864443 (GRCh37)
Canonical SPDI:: NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATATATATATATAT,NC_000003.12:53830402:TATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATAT
Gene:: CHDH (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATATAT=0./0 (ALFA)
TA=0.21486/1076 (1000Genomes)
HGVS:: NC_000003.12:g.53830404AT[6], NC_000003.12:g.53830404AT[7], NC_000003.12:g.53830404AT[8], NC_000003.12:g.53830404AT[10], NC_000003.12:g.53830404AT[11], NC_000003.12:g.53830404AT[12], NC_000003.12:g.53830404AT[13], NC_000003.12:g.53830404AT[14], NC_000003.12:g.53830404AT[15], NC_000003.12:g.53830404AT[16], NC_000003.12:g.53830404AT[17], NC_000003.12:g.53830404AT[18], NC_000003.12:g.53830404AT[19], NC_000003.11:g.53864431AT[6], NC_000003.11:g.53864431AT[7], NC_000003.11:g.53864431AT[8], NC_000003.11:g.53864431AT[10], NC_000003.11:g.53864431AT[11], NC_000003.11:g.53864431AT[12], NC_000003.11:g.53864431AT[13], NC_000003.11:g.53864431AT[14], NC_000003.11:g.53864431AT[15], NC_000003.11:g.53864431AT[16], NC_000003.11:g.53864431AT[17], NC_000003.11:g.53864431AT[18], NC_000003.11:g.53864431AT[19], NG_028042.1:g.20974TA[6], NG_028042.1:g.20974TA[7], NG_028042.1:g.20974TA[8], NG_028042.1:g.20974TA[10], NG_028042.1:g.20974TA[11], NG_028042.1:g.20974TA[12], NG_028042.1:g.20974TA[13], NG_028042.1:g.20974TA[14], NG_028042.1:g.20974TA[15], NG_028042.1:g.20974TA[16], NG_028042.1:g.20974TA[17], NG_028042.1:g.20974TA[18], NG_028042.1:g.20974TA[19]

Select item 14910614438.

rs1491061443 has merged into rs59355780 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 3:53826326 (GRCh38)
3:53860353 (GRCh37)
Canonical SPDI:: NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAA,NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:53826315:AAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: CHDH (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
-=0.15/6 (GENOME_DK)
A=0.23734/389 (1000Genomes)
HGVS:: NC_000003.12:g.53826326_53826327del, NC_000003.12:g.53826327del, NC_000003.12:g.53826327dup, NC_000003.12:g.53826326_53826327dup, NC_000003.12:g.53826325_53826327dup, NC_000003.12:g.53826324_53826327dup, NC_000003.12:g.53826327_53826328insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.53860353_53860354del, NC_000003.11:g.53860354del, NC_000003.11:g.53860354dup, NC_000003.11:g.53860353_53860354dup, NC_000003.11:g.53860352_53860354dup, NC_000003.11:g.53860351_53860354dup, NC_000003.11:g.53860354_53860355insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_028042.1:g.25077_25078del, NG_028042.1:g.25078del, NG_028042.1:g.25078dup, NG_028042.1:g.25077_25078dup, NG_028042.1:g.25076_25078dup, NG_028042.1:g.25075_25078dup, NG_028042.1:g.25078_25079insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14909426049.

rs1490942604 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 3:53819141 (GRCh38)
3:53853168 (GRCh37)
Canonical SPDI:: NC_000003.12:53819140:A:C
Gene:: CHDH (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.53819141A>C, NC_000003.11:g.53853168A>C, NG_028042.1:g.32253T>G

Select item 149085822110.

rs1490858221 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:53834678 (GRCh38)
3:53868705 (GRCh37)
Canonical SPDI:: NC_000003.12:53834677:G:A
Gene:: CHDH (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000003.12:g.53834678G>A, NC_000003.11:g.53868705G>A, NG_028042.1:g.16716C>T

Select item 149082367211.

rs1490823672 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 3:53842030 (GRCh38)
3:53876057 (GRCh37)
Canonical SPDI:: NC_000003.12:53842029:C:A,NC_000003.12:53842029:C:T
Gene:: CHDH (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
HGVS:: NC_000003.12:g.53842030C>A, NC_000003.12:g.53842030C>T, NC_000003.11:g.53876057C>A, NC_000003.11:g.53876057C>T, NG_028042.1:g.9364G>T, NG_028042.1:g.9364G>A

Select item 149078369312.

rs1490783693 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:53827279 (GRCh38)
3:53861306 (GRCh37)
Canonical SPDI:: NC_000003.12:53827278:C:T
Gene:: CHDH (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000106/3 (TOMMO)
HGVS:: NC_000003.12:g.53827279C>T, NC_000003.11:g.53861306C>T, NG_028042.1:g.24115G>A

Select item 149066346413.

rs1490663464 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:53832486 (GRCh38)
3:53866513 (GRCh37)
Canonical SPDI:: NC_000003.12:53832485:C:T
Gene:: CHDH (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000003.12:g.53832486C>T, NC_000003.11:g.53866513C>T, NG_028042.1:g.18908G>A

Select item 149058187914.

rs1490581879 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>- [Show Flanks]
Chromosome:: 3:53812885 (GRCh38)
3:53846912 (GRCh37)
Canonical SPDI:: NC_000003.12:53812883:TTT:T
Gene:: CACNA1D (Varview), CHDH (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.000029/4 (GnomAD)
-=0.000042/11 (TOPMED)
HGVS:: NC_000003.12:g.53812885_53812886del, NC_000003.11:g.53846912_53846913del, NG_032999.1:g.322837_322838del, NM_000720.4:c.*1479_*1480del, NM_001128840.3:c.*1479_*1480del, NM_001128839.3:c.*1479_*1480del, NM_018397.5:c.*4892_*4893del, XM_005265448.4:c.*1479_*1480del, XM_005265448.2:c.*1479_*1480del, XM_005265448.1:c.*1479_*1480del, XM_011534097.3:c.*1479_*1480del, XM_011534097.2:c.*1479_*1480del, XM_011534097.1:c.*1479_*1480del, XM_011534094.3:c.*1479_*1480del, XM_011534094.2:c.*1479_*1480del, XM_011534094.1:c.*1479_*1480del, XM_011534100.3:c.*1479_*1480del, XM_011534100.2:c.*1479_*1480del, XM_011534100.1:c.*1479_*1480del, XM_011534096.3:c.*1479_*1480del, XM_011534096.1:c.*1479_*1480del, XM_011534099.3:c.*1479_*1480del, XM_011534099.2:c.*1479_*1480del, XM_011534099.1:c.*1479_*1480del, XM_017007137.2:c.*1479_*1480del, XM_017007137.1:c.*1479_*1480del, XM_017007138.2:c.*1479_*1480del, XM_017007138.1:c.*1479_*1480del, XM_017007139.2:c.*1479_*1480del, XM_017007139.1:c.*1479_*1480del, XM_017007141.2:c.*1479_*1480del, XM_017007141.1:c.*1479_*1480del, XM_017007140.2:c.*1479_*1480del, XM_017007140.1:c.*1479_*1480del, XM_017007144.2:c.*1479_*1480del, XM_017007143.2:c.*1479_*1480del, XM_017007143.1:c.*1479_*1480del, XM_017007142.2:c.*1479_*1480del, XM_017007142.1:c.*1479_*1480del, XM_017007145.2:c.*1479_*1480del, XM_017007145.1:c.*1479_*1480del, XM_047448871.1:c.*1479_*1480del, XM_047448872.1:c.*1479_*1480del

Select item 149057391015.

rs1490573910 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:53826133 (GRCh38)
3:53860160 (GRCh37)
Canonical SPDI:: NC_000003.12:53826132:A:G
Gene:: CHDH (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.53826133A>G, NC_000003.11:g.53860160A>G, NG_028042.1:g.25261T>C

Select item 149049572016.

rs1490495720 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:53833163 (GRCh38)
3:53867190 (GRCh37)
Canonical SPDI:: NC_000003.12:53833162:G:T
Gene:: CHDH (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000003.12:g.53833163G>T, NC_000003.11:g.53867190G>T, NG_028042.1:g.18231C>A

Select item 149042690217.

rs1490426902 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:53847947 (GRCh38)
3:53881974 (GRCh37)
Canonical SPDI:: NC_000003.12:53847946:T:C
Gene:: CHDH (Varview), IL17RB (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.53847947T>C, NC_000003.11:g.53881974T>C, NG_028042.1:g.3447A>G

Select item 149025688918.

rs1490256889 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AAGT [Show Flanks]
Chromosome:: 3:53813589 (GRCh38)
3:53847617 (GRCh37)
Canonical SPDI:: NC_000003.12:53813589:TAAGT:TAAGTAAGT
Gene:: CACNA1D (Varview), CHDH (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TAAGTAAGT=0./0 (ALFA)
TAAG=0.000004/1 (TOPMED)
TAAG=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.53813591_53813594dup, NC_000003.11:g.53847618_53847621dup, NG_032999.1:g.323543_323546dup, NM_000720.4:c.*2185_*2188dup, NM_001128840.3:c.*2185_*2188dup, NM_001128839.3:c.*2185_*2188dup, NM_018397.5:c.*4184_*4187dup, XM_005265448.4:c.*2185_*2188dup, XM_011534097.3:c.*2185_*2188dup, XM_011534094.3:c.*2185_*2188dup, XM_011534100.3:c.*2185_*2188dup, XM_011534096.3:c.*2185_*2188dup, XM_011534099.3:c.*2185_*2188dup, XM_017007137.2:c.*2185_*2188dup, XM_017007138.2:c.*2185_*2188dup, XM_017007139.2:c.*2185_*2188dup, XM_017007141.2:c.*2185_*2188dup, XM_017007140.2:c.*2185_*2188dup, XM_017007144.2:c.*2185_*2188dup, XM_017007143.2:c.*2185_*2188dup, XM_017007142.2:c.*2185_*2188dup, XM_017007145.2:c.*2185_*2188dup, XM_047448871.1:c.*2185_*2188dup, XM_047448872.1:c.*2185_*2188dup

Select item 149022235419.

rs1490222354 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 3:53812761 (GRCh38)
3:53846789 (GRCh37)
Canonical SPDI:: NC_000003.12:53812761:T:TT
Gene:: CACNA1D (Varview), CHDH (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000042/11 (TOPMED)
HGVS:: NC_000003.12:g.53812762dup, NC_000003.11:g.53846789dup, NG_032999.1:g.322714dup, NM_000720.4:c.*1356dup, NM_001128840.3:c.*1356dup, NM_001128839.3:c.*1356dup, NM_018397.5:c.*5015dup, XM_005265448.4:c.*1356dup, XM_005265448.2:c.*1356dup, XM_005265448.1:c.*1356dup, XM_011534097.3:c.*1356dup, XM_011534097.2:c.*1356dup, XM_011534097.1:c.*1356dup, XM_011534094.3:c.*1356dup, XM_011534094.2:c.*1356dup, XM_011534094.1:c.*1356dup, XM_011534100.3:c.*1356dup, XM_011534100.2:c.*1356dup, XM_011534100.1:c.*1356dup, XM_011534096.3:c.*1356dup, XM_011534096.1:c.*1356dup, XM_011534099.3:c.*1356dup, XM_011534099.2:c.*1356dup, XM_011534099.1:c.*1356dup, XM_017007137.2:c.*1356dup, XM_017007137.1:c.*1356dup, XM_017007138.2:c.*1356dup, XM_017007138.1:c.*1356dup, XM_017007139.2:c.*1356dup, XM_017007139.1:c.*1356dup, XM_017007141.2:c.*1356dup, XM_017007141.1:c.*1356dup, XM_017007140.2:c.*1356dup, XM_017007140.1:c.*1356dup, XM_017007144.2:c.*1356dup, XM_017007143.2:c.*1356dup, XM_017007143.1:c.*1356dup, XM_017007142.2:c.*1356dup, XM_017007142.1:c.*1356dup, XM_017007145.2:c.*1356dup, XM_017007145.1:c.*1356dup, XM_047448871.1:c.*1356dup, XM_047448872.1:c.*1356dup

Select item 149021413820.

rs1490214138 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 3:53844984 (GRCh38)
3:53879011 (GRCh37)
Canonical SPDI:: NC_000003.12:53844983:C:A
Gene:: CHDH (Varview), IL17RB (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.53844984C>A, NC_000003.11:g.53879011C>A, NG_028042.1:g.6410G>T

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