SNP Links for Gene (Select 1611) - SNP

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Select item 14915630911.

rs1491563091 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTA [Show Flanks]
Chromosome:: 5:10722578 (GRCh38)
5:10722691 (GRCh37)
Canonical SPDI:: NC_000005.10:10722578:TA:TACTA
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: TAC=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.10722580_10722581insCTA, NC_000005.9:g.10722692_10722693insCTA, NG_011546.1:g.43697_43698insGTA

Select item 14915541532.

rs1491554153 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GCAT [Show Flanks]
Chromosome:: 5:10722576 (GRCh38)
5:10722689 (GRCh37)
Canonical SPDI:: NC_000005.10:10722576:CAT:CATGCAT
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CATGCAT=0./0 (ALFA)
CATG=0.000008/1 (GnomAD)
CATG=0.000011/3 (TOPMED)
HGVS:: NC_000005.10:g.10722579_10722580insGCAT, NC_000005.9:g.10722691_10722692insGCAT, NG_011546.1:g.43699_43700insCATG

Select item 14915418193.

rs1491541819 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A,AA [Show Flanks]
Chromosome:: 5:10693125 (GRCh38)
5:10693238 (GRCh37)
Canonical SPDI:: NC_000005.10:10693125:A:AA,NC_000005.10:10693125:A:AAA
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAA=0./0 (ALFA)
HGVS:: NC_000005.10:g.10693126dup, NC_000005.10:g.10693126_10693127insAA, NC_000005.9:g.10693238dup, NC_000005.9:g.10693238_10693239insAA, NG_011546.1:g.73150dup, NG_011546.1:g.73150_73151insTT

Select item 14914245464.

rs1491424546 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 5:10689888 (GRCh38)
5:10690000 (GRCh37)
Canonical SPDI:: NC_000005.10:10689887:AG:
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.10689888_10689889del, NC_000005.9:g.10690000_10690001del, NG_011546.1:g.76387_76388del

Select item 14914054315.

rs1491405431 has merged into rs10596228 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACACACACACACAC>-,AC,ACAC,ACACAC,ACACACAC,ACACACACAC,ACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC [Show Flanks]
Chromosome:: 5:10693140 (GRCh38)
5:10693252 (GRCh37)
Canonical SPDI:: NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACAC,NC_000005.10:10693124:CACACACACACACACACACACACACACAC:CACACACACACACACACACACACACACACACACACACACACACACAC
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACACACAC=0./0 (ALFA)
CACACACA=0.00102/270 (TOPMED)
CACACA=0.426717/2137 (1000Genomes)
HGVS:: NC_000005.10:g.10693126AC[7], NC_000005.10:g.10693126AC[8], NC_000005.10:g.10693126AC[9], NC_000005.10:g.10693126AC[10], NC_000005.10:g.10693126AC[11], NC_000005.10:g.10693126AC[12], NC_000005.10:g.10693126AC[13], NC_000005.10:g.10693126AC[15], NC_000005.10:g.10693126AC[16], NC_000005.10:g.10693126AC[17], NC_000005.10:g.10693126AC[18], NC_000005.10:g.10693126AC[19], NC_000005.10:g.10693126AC[20], NC_000005.10:g.10693126AC[21], NC_000005.10:g.10693126AC[22], NC_000005.10:g.10693126AC[23], NC_000005.9:g.10693238AC[7], NC_000005.9:g.10693238AC[8], NC_000005.9:g.10693238AC[9], NC_000005.9:g.10693238AC[10], NC_000005.9:g.10693238AC[11], NC_000005.9:g.10693238AC[12], NC_000005.9:g.10693238AC[13], NC_000005.9:g.10693238AC[15], NC_000005.9:g.10693238AC[16], NC_000005.9:g.10693238AC[17], NC_000005.9:g.10693238AC[18], NC_000005.9:g.10693238AC[19], NC_000005.9:g.10693238AC[20], NC_000005.9:g.10693238AC[21], NC_000005.9:g.10693238AC[22], NC_000005.9:g.10693238AC[23], NG_011546.1:g.73124TG[7], NG_011546.1:g.73124TG[8], NG_011546.1:g.73124TG[9], NG_011546.1:g.73124TG[10], NG_011546.1:g.73124TG[11], NG_011546.1:g.73124TG[12], NG_011546.1:g.73124TG[13], NG_011546.1:g.73124TG[15], NG_011546.1:g.73124TG[16], NG_011546.1:g.73124TG[17], NG_011546.1:g.73124TG[18], NG_011546.1:g.73124TG[19], NG_011546.1:g.73124TG[20], NG_011546.1:g.73124TG[21], NG_011546.1:g.73124TG[22], NG_011546.1:g.73124TG[23]

Select item 14913994286.

rs1491399428 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->TAAA
Chromosome:: no mapping
Canonical SPDI:

Select item 14913954237.

rs1491395423 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 5:10746333 (GRCh38)
5:10746445 (GRCh37)
Canonical SPDI:: NC_000005.10:10746331:TGT:T
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000506/6 (ALFA)
-=0.000544/67 (GnomAD)
-=0.000781/5 (1000Genomes)
HGVS:: NC_000005.10:g.10746333_10746334del, NC_000005.9:g.10746445_10746446del, NG_011546.1:g.19943_19944del

Select item 14913166398.

rs1491316639 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 5:10687928 (GRCh38)
5:10688040 (GRCh37)
Canonical SPDI:: NC_000005.10:10687927:TA:
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000008/1 (GnomAD)
HGVS:: NC_000005.10:g.10687928_10687929del, NC_000005.9:g.10688040_10688041del, NG_011546.1:g.78347_78348del

Select item 14912452009.

rs1491245200 has merged into rs1207672031 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATATA>-,TA,TATA,TATATATA,TATATATATA [Show Flanks]
Chromosome:: 5:10722581 (GRCh38)
5:10722693 (GRCh37)
Canonical SPDI:: NC_000005.10:10722577:ATATATATA:ATA,NC_000005.10:10722577:ATATATATA:ATATA,NC_000005.10:10722577:ATATATATA:ATATATA,NC_000005.10:10722577:ATATATATA:ATATATATATA,NC_000005.10:10722577:ATATATATA:ATATATATATATA
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATA=0./0 (ALFA)
HGVS:: NC_000005.10:g.10722579TA[1], NC_000005.10:g.10722579TA[2], NC_000005.10:g.10722579TA[3], NC_000005.10:g.10722579TA[5], NC_000005.10:g.10722579TA[6], NC_000005.9:g.10722691TA[1], NC_000005.9:g.10722691TA[2], NC_000005.9:g.10722691TA[3], NC_000005.9:g.10722691TA[5], NC_000005.9:g.10722691TA[6], NG_011546.1:g.43691AT[1], NG_011546.1:g.43691AT[2], NG_011546.1:g.43691AT[3], NG_011546.1:g.43691AT[5], NG_011546.1:g.43691AT[6]

Select item 149121881110.

rs1491218811 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 5:10686643 (GRCh38)
5:10686755 (GRCh37)
Canonical SPDI:: NC_000005.10:10686642:AA:
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000014/2 (GnomAD)
-=0.000026/7 (TOPMED)
HGVS:: NC_000005.10:g.10686643_10686644del, NC_000005.9:g.10686755_10686756del, NG_011546.1:g.79632_79633del

Select item 149120453511.

rs1491204535 has merged into rs10644743 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 5:10739209 (GRCh38)
5:10739321 (GRCh37)
Canonical SPDI:: NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000005.10:10739201:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAA=0./0 (ALFA)
AAAAAAAAAAAAAAAAA=0./0 (GENOME_DK)
HGVS:: NC_000005.10:g.10739209_10739226del, NC_000005.10:g.10739210_10739226del, NC_000005.10:g.10739212_10739226del, NC_000005.10:g.10739213_10739226del, NC_000005.10:g.10739214_10739226del, NC_000005.10:g.10739215_10739226del, NC_000005.10:g.10739216_10739226del, NC_000005.10:g.10739217_10739226del, NC_000005.10:g.10739218_10739226del, NC_000005.10:g.10739219_10739226del, NC_000005.10:g.10739220_10739226del, NC_000005.10:g.10739221_10739226del, NC_000005.10:g.10739222_10739226del, NC_000005.10:g.10739223_10739226del, NC_000005.10:g.10739224_10739226del, NC_000005.10:g.10739225_10739226del, NC_000005.10:g.10739226del, NC_000005.10:g.10739226dup, NC_000005.10:g.10739225_10739226dup, NC_000005.10:g.10739224_10739226dup, NC_000005.10:g.10739223_10739226dup, NC_000005.10:g.10739222_10739226dup, NC_000005.10:g.10739221_10739226dup, NC_000005.10:g.10739220_10739226dup, NC_000005.10:g.10739219_10739226dup, NC_000005.10:g.10739218_10739226dup, NC_000005.10:g.10739214_10739226dup, NC_000005.10:g.10739213_10739226dup, NC_000005.10:g.10739209_10739226dup, NC_000005.10:g.10739208_10739226dup, NC_000005.10:g.10739207_10739226dup, NC_000005.10:g.10739206_10739226dup, NC_000005.10:g.10739205_10739226dup, NC_000005.10:g.10739203_10739226dup, NC_000005.10:g.10739226_10739227insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000005.9:g.10739321_10739338del, NC_000005.9:g.10739322_10739338del, NC_000005.9:g.10739324_10739338del, NC_000005.9:g.10739325_10739338del, NC_000005.9:g.10739326_10739338del, NC_000005.9:g.10739327_10739338del, NC_000005.9:g.10739328_10739338del, NC_000005.9:g.10739329_10739338del, NC_000005.9:g.10739330_10739338del, NC_000005.9:g.10739331_10739338del, NC_000005.9:g.10739332_10739338del, NC_000005.9:g.10739333_10739338del, NC_000005.9:g.10739334_10739338del, NC_000005.9:g.10739335_10739338del, NC_000005.9:g.10739336_10739338del, NC_000005.9:g.10739337_10739338del, NC_000005.9:g.10739338del, NC_000005.9:g.10739338dup, NC_000005.9:g.10739337_10739338dup, NC_000005.9:g.10739336_10739338dup, NC_000005.9:g.10739335_10739338dup, NC_000005.9:g.10739334_10739338dup, NC_000005.9:g.10739333_10739338dup, NC_000005.9:g.10739332_10739338dup, NC_000005.9:g.10739331_10739338dup, NC_000005.9:g.10739330_10739338dup, NC_000005.9:g.10739326_10739338dup, NC_000005.9:g.10739325_10739338dup, NC_000005.9:g.10739321_10739338dup, NC_000005.9:g.10739320_10739338dup, NC_000005.9:g.10739319_10739338dup, NC_000005.9:g.10739318_10739338dup, NC_000005.9:g.10739317_10739338dup, NC_000005.9:g.10739315_10739338dup, NC_000005.9:g.10739338_10739339insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_011546.1:g.27057_27074del, NG_011546.1:g.27058_27074del, NG_011546.1:g.27060_27074del, NG_011546.1:g.27061_27074del, NG_011546.1:g.27062_27074del, NG_011546.1:g.27063_27074del, NG_011546.1:g.27064_27074del, NG_011546.1:g.27065_27074del, NG_011546.1:g.27066_27074del, NG_011546.1:g.27067_27074del, NG_011546.1:g.27068_27074del, NG_011546.1:g.27069_27074del, NG_011546.1:g.27070_27074del, NG_011546.1:g.27071_27074del, NG_011546.1:g.27072_27074del, NG_011546.1:g.27073_27074del, NG_011546.1:g.27074del, NG_011546.1:g.27074dup, NG_011546.1:g.27073_27074dup, NG_011546.1:g.27072_27074dup, NG_011546.1:g.27071_27074dup, NG_011546.1:g.27070_27074dup, NG_011546.1:g.27069_27074dup, NG_011546.1:g.27068_27074dup, NG_011546.1:g.27067_27074dup, NG_011546.1:g.27066_27074dup, NG_011546.1:g.27062_27074dup, NG_011546.1:g.27061_27074dup, NG_011546.1:g.27057_27074dup, NG_011546.1:g.27056_27074dup, NG_011546.1:g.27055_27074dup, NG_011546.1:g.27054_27074dup, NG_011546.1:g.27053_27074dup, NG_011546.1:g.27051_27074dup, NG_011546.1:g.27074_27075insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149113000212.

rs1491130002 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 5:10722577 (GRCh38)
5:10722689 (GRCh37)
Canonical SPDI:: NC_000005.10:10722575:ACA:A
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000023/3 (GnomAD)
HGVS:: NC_000005.10:g.10722577_10722578del, NC_000005.9:g.10722689_10722690del, NG_011546.1:g.43699_43700del

Select item 149109614613.

rs1491096146 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TG [Show Flanks]
Chromosome:: 5:10689888 (GRCh38)
5:10690001 (GRCh37)
Canonical SPDI:: NC_000005.10:10689888:GTG:GTGTG
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGTG=0./0 (ALFA)
GT=0.000015/4 (TOPMED)
GT=0.000021/3 (GnomAD)
HGVS:: NC_000005.10:g.10689890_10689891dup, NC_000005.9:g.10690002_10690003dup, NG_011546.1:g.76386_76387dup

Select item 149096916314.

rs1490969163 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:10696337 (GRCh38)
5:10696449 (GRCh37)
Canonical SPDI:: NC_000005.10:10696336:G:A
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.10696337G>A, NC_000005.9:g.10696449G>A, NG_011546.1:g.69939C>T

Select item 149092996115.

rs1490929961 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:10694255 (GRCh38)
5:10694367 (GRCh37)
Canonical SPDI:: NC_000005.10:10694254:C:T
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000035/1 (TOMMO)
T=0.000546/1 (Korea1K)
HGVS:: NC_000005.10:g.10694255C>T, NC_000005.9:g.10694367C>T, NG_011546.1:g.72021G>A

Select item 149086986716.

rs1490869867 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:10746894 (GRCh38)
5:10747006 (GRCh37)
Canonical SPDI:: NC_000005.10:10746893:A:G
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.10746894A>G, NC_000005.9:g.10747006A>G, NG_011546.1:g.19382T>C

Select item 149080559817.

rs1490805598 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:10752026 (GRCh38)
5:10752138 (GRCh37)
Canonical SPDI:: NC_000005.10:10752025:T:C
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000005.10:g.10752026T>C, NC_000005.9:g.10752138T>C, NG_011546.1:g.14250A>G

Select item 149077496018.

rs1490774960 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 5:10762723 (GRCh38)
5:10762835 (GRCh37)
Canonical SPDI:: NC_000005.10:10762722:G:A,NC_000005.10:10762722:G:T
Gene:: DAP (Varview), DAP-DT (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000005.10:g.10762723G>A, NC_000005.10:g.10762723G>T, NC_000005.9:g.10762835G>A, NC_000005.9:g.10762835G>T, NG_011546.1:g.3553C>T, NG_011546.1:g.3553C>A, XR_002956210.2:n.1247G>A, XR_002956210.2:n.1247G>T

Select item 149075104019.

rs1490751040 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 5:10716338 (GRCh38)
5:10716450 (GRCh37)
Canonical SPDI:: NC_000005.10:10716337:G:A,NC_000005.10:10716337:G:T
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.10716338G>A, NC_000005.10:g.10716338G>T, NC_000005.9:g.10716450G>A, NC_000005.9:g.10716450G>T, NG_011546.1:g.49938C>T, NG_011546.1:g.49938C>A

Select item 149072594920.

rs1490725949 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 5:10730874 (GRCh38)
5:10730986 (GRCh37)
Canonical SPDI:: NC_000005.10:10730873:G:A,NC_000005.10:10730873:G:T
Gene:: DAP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: T=0.000009/1 (GnomAD)
A=0.000169/4 (TOMMO)
HGVS:: NC_000005.10:g.10730874G>A, NC_000005.10:g.10730874G>T, NC_000005.9:g.10730986G>A, NC_000005.9:g.10730986G>T, NG_011546.1:g.35402C>T, NG_011546.1:g.35402C>A

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