SNP Links for Gene (Select 100128594) - SNP

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Select item 14915762751.

rs1491576275 has merged into rs201637583 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: X:103917446 (GRCh38)
X:103172041 (GRCh37)
Canonical SPDI:: NC_000023.11:103917445:TG:
Gene:: TMSB15B (Varview), TMSB15B-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.07902/1458 (ALFA)
-=0.00001/1 (GnomAD)
-=0.00005/1 (TOMMO)
-=0.37591/1086 (ALSPAC)
-=0.3781/1402 (TWINSUK)
-=0.38199/1442 (1000Genomes)
-=0.425/17 (GENOME_DK)
HGVS:: NC_000023.11:g.103917446_103917447del, NW_004070885.1:g.53862_53863del, NC_000023.10:g.103172041_103172042del, NR_146556.1:n.1204_1205del

Select item 14913620292.

rs1491362029 has merged into rs782307917 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTTTT [Show Flanks]
Chromosome:: X:103922094 (GRCh38)
X:103176675 (GRCh37)
Canonical SPDI:: NC_000023.11:103922085:TTTTTTTTTTTTTT:TTTTTTTT,NC_000023.11:103922085:TTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000023.11:103922085:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000023.11:103922085:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000023.11:103922085:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000023.11:103922085:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT
Gene:: TMSB15B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
-=0.175/7 (GENOME_DK)
HGVS:: NC_000023.11:g.103922094_103922099del, NC_000023.11:g.103922097_103922099del, NC_000023.11:g.103922098_103922099del, NC_000023.11:g.103922099del, NC_000023.11:g.103922099dup, NC_000023.11:g.103922096_103922099dup, NW_004070885.1:g.58510_58515del, NW_004070885.1:g.58513_58515del, NW_004070885.1:g.58514_58515del, NW_004070885.1:g.58515del, NW_004070885.1:g.58515dup, NW_004070885.1:g.58512_58515dup, NC_000023.10:g.103176675_103176680del, NC_000023.10:g.103176678_103176680del, NC_000023.10:g.103176679_103176680del, NC_000023.10:g.103176680del, NC_000023.10:g.103176680dup, NC_000023.10:g.103176677_103176680dup

Select item 14913327783.

rs1491332778 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: X:103922086 (GRCh38)
X:103176668 (GRCh37)
Canonical SPDI:: NC_000023.11:103922086::C
Gene:: TMSB15B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00005/1 (TOMMO)
C=0.0001/9 (GnomAD)
HGVS:: NC_000023.11:g.103922086_103922087insC, NW_004070885.1:g.58502_58503insC, NC_000023.10:g.103176667_103176668insC

Select item 14911103614.

rs1491110361 has merged into rs551801081 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGGGGGG>-,GGGGG,GGGGGG,GGGGGGGG,GGGGGGGGG [Show Flanks]
Chromosome:: X:103917450 (GRCh38)
X:103172045 (GRCh37)
Canonical SPDI:: NC_000023.11:103917446:GGGGGGGGGG:GGG,NC_000023.11:103917446:GGGGGGGGGG:GGGGGGGG,NC_000023.11:103917446:GGGGGGGGGG:GGGGGGGGG,NC_000023.11:103917446:GGGGGGGGGG:GGGGGGGGGGG,NC_000023.11:103917446:GGGGGGGGGG:GGGGGGGGGGGG
Gene:: TMSB15B (Varview), TMSB15B-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGGGG=0./0 (ALFA)
-=0.00093/12 (TOMMO)
HGVS:: NC_000023.11:g.103917450_103917456del, NC_000023.11:g.103917455_103917456del, NC_000023.11:g.103917456del, NC_000023.11:g.103917456dup, NC_000023.11:g.103917455_103917456dup, NW_004070885.1:g.53866_53872del, NW_004070885.1:g.53871_53872del, NW_004070885.1:g.53872del, NW_004070885.1:g.53872dup, NW_004070885.1:g.53871_53872dup, NC_000023.10:g.103172045_103172051del, NC_000023.10:g.103172050_103172051del, NC_000023.10:g.103172051del, NC_000023.10:g.103172051dup, NC_000023.10:g.103172050_103172051dup, NR_146556.1:n.1198_1204del, NR_146556.1:n.1203_1204del, NR_146556.1:n.1204del, NR_146556.1:n.1204dup, NR_146556.1:n.1203_1204dup

Select item 14909894885.

rs1490989488 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:103893475 (GRCh38)
X:103148396 (GRCh37)
Canonical SPDI:: NC_000023.11:103893474:T:C
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000013/1 (GnomAD)
HGVS:: NC_000023.11:g.103893475T>C, NW_004070885.1:g.29891T>C, NC_000023.10:g.103148396T>C

Select item 14909832486.

rs1490983248 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:103892637 (GRCh38)
X:103147558 (GRCh37)
Canonical SPDI:: NC_000023.11:103892636:T:G
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.103892637T>G, NW_004070885.1:g.29053T>G, NC_000023.10:g.103147558T>G

Select item 14908128127.

rs1490812812 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: X:103917382 (GRCh38)
X:103171976 (GRCh37)
Canonical SPDI:: NC_000023.11:103917381:C:A,NC_000023.11:103917381:C:T
Gene:: TMSB15B (Varview), TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,downstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00002/2 (GnomAD)
A=0.00171/5 (KOREAN)
HGVS:: NC_000023.11:g.103917382C>A, NC_000023.11:g.103917382C>T, NW_004070885.1:g.53798C>A, NW_004070885.1:g.53798C>T, NC_000023.10:g.103171976C>A, NC_000023.10:g.103171976C>T

Select item 14907899508.

rs1490789950 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:103899063 (GRCh38)
X:103153984 (GRCh37)
Canonical SPDI:: NC_000023.11:103899062:A:T
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.00006/5 (GnomAD)
HGVS:: NC_000023.11:g.103899063A>T, NW_004070885.1:g.35479A>T, NC_000023.10:g.103153984A>T

Select item 14906953509.

rs1490695350 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:103884032 (GRCh38)
X:103138953 (GRCh37)
Canonical SPDI:: NC_000023.11:103884031:G:A
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103884032G>A, NW_004070885.1:g.20448G>A, NC_000023.10:g.103138953G>A

Select item 149064977210.

rs1490649772 has merged into rs4006716 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATATATATATATATATATATATATATA>-,TA,TATA,TATATA,TATATATA,TATATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATA,TATATATATATATATATATA,TATATATATATATATATATATA,TATATATATATATATATATATATA,TATATATATATATATATATATATATA,TATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATATA [Show Flanks]
Chromosome:: X:103917655 (GRCh38)
X:103172250 (GRCh37)
Canonical SPDI:: NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000023.11:103917644:TATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
Gene:: TMSB15B (Varview), TMSB15B-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATA=0./0 (ALFA)
HGVS:: NC_000023.11:g.103917645TA[5], NC_000023.11:g.103917645TA[6], NC_000023.11:g.103917645TA[7], NC_000023.11:g.103917645TA[8], NC_000023.11:g.103917645TA[9], NC_000023.11:g.103917645TA[10], NC_000023.11:g.103917645TA[11], NC_000023.11:g.103917645TA[12], NC_000023.11:g.103917645TA[13], NC_000023.11:g.103917645TA[14], NC_000023.11:g.103917645TA[15], NC_000023.11:g.103917645TA[16], NC_000023.11:g.103917645TA[17], NC_000023.11:g.103917645TA[18], NC_000023.11:g.103917645TA[20], NC_000023.11:g.103917645TA[21], NC_000023.11:g.103917645TA[22], NC_000023.11:g.103917645TA[23], NC_000023.11:g.103917645TA[24], NC_000023.11:g.103917645TA[25], NC_000023.11:g.103917645TA[26], NC_000023.11:g.103917645TA[27], NC_000023.11:g.103917645TA[28], NC_000023.11:g.103917645TA[29], NC_000023.11:g.103917645TA[30], NC_000023.11:g.103917645TA[31], NC_000023.11:g.103917645TA[32], NW_004070885.1:g.54061TA[5], NW_004070885.1:g.54061TA[6], NW_004070885.1:g.54061TA[7], NW_004070885.1:g.54061TA[8], NW_004070885.1:g.54061TA[9], NW_004070885.1:g.54061TA[10], NW_004070885.1:g.54061TA[11], NW_004070885.1:g.54061TA[12], NW_004070885.1:g.54061TA[13], NW_004070885.1:g.54061TA[14], NW_004070885.1:g.54061TA[15], NW_004070885.1:g.54061TA[16], NW_004070885.1:g.54061TA[17], NW_004070885.1:g.54061TA[18], NW_004070885.1:g.54061TA[20], NW_004070885.1:g.54061TA[21], NW_004070885.1:g.54061TA[22], NW_004070885.1:g.54061TA[23], NW_004070885.1:g.54061TA[24], NW_004070885.1:g.54061TA[25], NW_004070885.1:g.54061TA[26], NW_004070885.1:g.54061TA[27], NW_004070885.1:g.54061TA[28], NW_004070885.1:g.54061TA[29], NW_004070885.1:g.54061TA[30], NW_004070885.1:g.54061TA[31], NW_004070885.1:g.54061TA[32], NC_000023.10:g.103172240TA[19], NC_000023.10:g.103172240TA[5], NC_000023.10:g.103172240TA[6], NC_000023.10:g.103172240TA[7], NC_000023.10:g.103172240TA[8], NC_000023.10:g.103172240TA[9], NC_000023.10:g.103172240TA[10], NC_000023.10:g.103172240TA[11], NC_000023.10:g.103172240TA[12], NC_000023.10:g.103172240TA[14], NC_000023.10:g.103172240TA[15], NC_000023.10:g.103172240TA[16], NC_000023.10:g.103172240TA[17], NC_000023.10:g.103172240TA[18], NC_000023.10:g.103172240TA[20], NC_000023.10:g.103172240TA[21], NC_000023.10:g.103172240TA[22], NC_000023.10:g.103172240TA[23], NC_000023.10:g.103172240TA[24], NC_000023.10:g.103172240TA[25], NC_000023.10:g.103172240TA[26], NC_000023.10:g.103172240TA[27], NC_000023.10:g.103172240TA[28], NC_000023.10:g.103172240TA[29], NC_000023.10:g.103172240TA[30], NC_000023.10:g.103172240TA[31], NC_000023.10:g.103172240TA[32], NR_146556.1:n.969TA[5], NR_146556.1:n.969TA[6], NR_146556.1:n.969TA[7], NR_146556.1:n.969TA[8], NR_146556.1:n.969TA[9], NR_146556.1:n.969TA[10], NR_146556.1:n.969TA[11], NR_146556.1:n.969TA[12], NR_146556.1:n.969TA[13], NR_146556.1:n.969TA[14], NR_146556.1:n.969TA[15], NR_146556.1:n.969TA[16], NR_146556.1:n.969TA[17], NR_146556.1:n.969TA[18], NR_146556.1:n.969TA[20], NR_146556.1:n.969TA[21], NR_146556.1:n.969TA[22], NR_146556.1:n.969TA[23], NR_146556.1:n.969TA[24], NR_146556.1:n.969TA[25], NR_146556.1:n.969TA[26], NR_146556.1:n.969TA[27], NR_146556.1:n.969TA[28], NR_146556.1:n.969TA[29], NR_146556.1:n.969TA[30], NR_146556.1:n.969TA[31], NR_146556.1:n.969TA[32]

Select item 149063002311.

rs1490630023 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:103899360 (GRCh38)
X:103154281 (GRCh37)
Canonical SPDI:: NC_000023.11:103899359:T:G
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000011/1 (GnomAD)
HGVS:: NC_000023.11:g.103899360T>G, NW_004070885.1:g.35776T>G, NC_000023.10:g.103154281T>G

Select item 149060719312.

rs1490607193 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:103887062 (GRCh38)
X:103141983 (GRCh37)
Canonical SPDI:: NC_000023.11:103887061:T:C
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000023/6 (TOPMED)
HGVS:: NC_000023.11:g.103887062T>C, NW_004070885.1:g.23478T>C, NC_000023.10:g.103141983T>C

Select item 149055606013.

rs1490556060 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:103898575 (GRCh38)
X:103153496 (GRCh37)
Canonical SPDI:: NC_000023.11:103898574:T:C
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000011/1 (GnomAD)
HGVS:: NC_000023.11:g.103898575T>C, NW_004070885.1:g.34991T>C, NC_000023.10:g.103153496T>C

Select item 149053510514.

rs1490535105 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: X:103885877 (GRCh38)
X:103140798 (GRCh37)
Canonical SPDI:: NC_000023.11:103885876:G:A,NC_000023.11:103885876:G:T
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103885877G>A, NC_000023.11:g.103885877G>T, NW_004070885.1:g.22293G>A, NW_004070885.1:g.22293G>T, NC_000023.10:g.103140798G>A, NC_000023.10:g.103140798G>T

Select item 149037254015.

rs1490372540 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:103905586 (GRCh38)
X:103160507 (GRCh37)
Canonical SPDI:: NC_000023.11:103905585:G:A
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103905586G>A, NW_004070885.1:g.42002G>A, NC_000023.10:g.103160507G>A

Select item 149032619416.

rs1490326194 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:103916572 (GRCh38)
X:103171166 (GRCh37)
Canonical SPDI:: NC_000023.11:103916571:T:C
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000142/2 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.103916572T>C, NW_004070885.1:g.52988T>C, NC_000023.10:g.103171166T>C

Select item 149030328117.

rs1490303281 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:103898601 (GRCh38)
X:103153522 (GRCh37)
Canonical SPDI:: NC_000023.11:103898600:G:C
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.00226/35 (ALFA)
C=0.00005/1 (TOMMO)
HGVS:: NC_000023.11:g.103898601G>C, NW_004070885.1:g.35017G>C, NC_000023.10:g.103153522G>C

Select item 149023226018.

rs1490232260 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: X:103897848 (GRCh38)
X:103152769 (GRCh37)
Canonical SPDI:: NC_000023.11:103897847:A:G,NC_000023.11:103897847:A:T
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.00028/25 (GnomAD)
HGVS:: NC_000023.11:g.103897848A>G, NC_000023.11:g.103897848A>T, NW_004070885.1:g.34264A>G, NW_004070885.1:g.34264A>T, NC_000023.10:g.103152769A>G, NC_000023.10:g.103152769A>T

Select item 149018857919.

rs1490188579 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:103883252 (GRCh38)
X:103138173 (GRCh37)
Canonical SPDI:: NC_000023.11:103883251:A:G
Gene:: TMSB15B-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103883252A>G, NW_004070885.1:g.19668A>G, NC_000023.10:g.103138173A>G

Select item 149006735120.

rs1490067351 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:103923729 (GRCh38)
X:103178310 (GRCh37)
Canonical SPDI:: NC_000023.11:103923728:A:G
Gene:: TMSB15B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00001/1 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.103923729A>G, NW_004070885.1:g.60145A>G, NC_000023.10:g.103178310A>G

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