SNP Links for Gene (Select 57716) - SNP

Links from Gene

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Select item 14915760641.

rs1491576064 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ACCCAGC,C [Show Flanks]
Chromosome:: 19:40399890 (GRCh38)
19:40905798 (GRCh37)
Canonical SPDI:: NC_000019.10:40399890:C:CACCCAGC,NC_000019.10:40399890:C:CC
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
HGVS:: NC_000019.10:g.40399891_40399892insACCCAGC, NC_000019.10:g.40399891dup, NC_000019.9:g.40905798_40905799insACCCAGC, NC_000019.9:g.40905798dup, NG_007979.1:g.18474_18475insCTGGGTG, NG_007979.1:g.18474dup

Select item 14915556492.

rs1491555649 [Homo sapiens]

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

Select item 14915434093.

rs1491543409 has merged into rs779452990 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 19:40399895 (GRCh38)
19:40905802 (GRCh37)
Canonical SPDI:: NC_000019.10:40399893:TCT:T,NC_000019.10:40399893:TCT:TCTCT
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCT=0./0 (ALFA)
TC=0.02427/90 (TWINSUK)
TC=0.025/1 (GENOME_DK)
TC=0.02595/100 (ALSPAC)
TC=0.0322/19 (NorthernSweden)
HGVS:: NC_000019.10:g.40399895_40399896del, NC_000019.10:g.40399895_40399896dup, NC_000019.9:g.40905802_40905803del, NC_000019.9:g.40905802_40905803dup, NG_007979.1:g.18470_18471del, NG_007979.1:g.18470_18471dup

Select item 14915371554.

rs1491537155 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GGTGTGTG [Show Flanks]
Chromosome:: 19:40407213 (GRCh38)
19:40913121 (GRCh37)
Canonical SPDI:: NC_000019.10:40407213:GTGTGTG:GTGTGTGGGTGTGTG
Gene:: PRX (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: GTGTGTGGGTGTGTG=0./0 (ALFA)
GTGTGTGG=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.40407214_40407220GT[3]GGGTGTGTG[1], NC_000019.9:g.40913121_40913127GT[3]GGGTGTGTG[1], NG_007979.1:g.11145_11151CA[3]CCCACACAC[1]

Select item 14915323455.

rs1491532345 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 19:40399866 (GRCh38)
19:40905774 (GRCh37)
Canonical SPDI:: NC_000019.10:40399866:C:CC
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
HGVS:: NC_000019.10:g.40399867dup, NC_000019.9:g.40905774dup, NG_007979.1:g.18498dup

Select item 14915313706.

rs1491531370 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 19:40399894 (GRCh38)
19:40905802 (GRCh37)
Canonical SPDI:: NC_000019.10:40399894:C:CC
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
HGVS:: NC_000019.10:g.40399895dup, NC_000019.9:g.40905802dup, NG_007979.1:g.18470dup

Select item 14914773257.

rs1491477325 has merged into rs974978665 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGAG>-,AG,AGAGAG,AGAGAGAG [Show Flanks]
Chromosome:: 19:40408854 (GRCh38)
19:40914761 (GRCh37)
Canonical SPDI:: NC_000019.10:40408846:GAGAGAGAGAG:GAGAGAG,NC_000019.10:40408846:GAGAGAGAGAG:GAGAGAGAG,NC_000019.10:40408846:GAGAGAGAGAG:GAGAGAGAGAGAG,NC_000019.10:40408846:GAGAGAGAGAG:GAGAGAGAGAGAGAG
Gene:: PRX (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAGAGAGAG=0./0 (ALFA)
-=0.00167/1 (NorthernSweden)
HGVS:: NC_000019.10:g.40408848AG[3], NC_000019.10:g.40408848AG[4], NC_000019.10:g.40408848AG[6], NC_000019.10:g.40408848AG[7], NC_000019.9:g.40914755AG[3], NC_000019.9:g.40914755AG[4], NC_000019.9:g.40914755AG[6], NC_000019.9:g.40914755AG[7], NG_007979.1:g.9509TC[3], NG_007979.1:g.9509TC[4], NG_007979.1:g.9509TC[6], NG_007979.1:g.9509TC[7]

Select item 14914699868.

rs1491469986 has merged into rs58039504 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT,TTTTTTTT [Show Flanks]
Chromosome:: 19:40416721 (GRCh38)
19:40922628 (GRCh37)
Canonical SPDI:: NC_000019.10:40416710:TTTTTTTTTTTTT:TTTTTTTTTT,NC_000019.10:40416710:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000019.10:40416710:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000019.10:40416710:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:40416710:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000019.10:40416710:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT
Gene:: PRX (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000019.10:g.40416721_40416723del, NC_000019.10:g.40416722_40416723del, NC_000019.10:g.40416723del, NC_000019.10:g.40416723dup, NC_000019.10:g.40416722_40416723dup, NC_000019.10:g.40416719_40416723dup, NC_000019.9:g.40922628_40922630del, NC_000019.9:g.40922629_40922630del, NC_000019.9:g.40922630del, NC_000019.9:g.40922630dup, NC_000019.9:g.40922629_40922630dup, NC_000019.9:g.40922626_40922630dup, NG_007979.1:g.1652_1654del, NG_007979.1:g.1653_1654del, NG_007979.1:g.1654del, NG_007979.1:g.1654dup, NG_007979.1:g.1653_1654dup, NG_007979.1:g.1650_1654dup

Select item 14914658909.

rs1491465890 has merged into rs1281344795 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT,CTCTCTCT [Show Flanks]
Chromosome:: 19:40399899 (GRCh38)
19:40905806 (GRCh37)
Canonical SPDI:: NC_000019.10:40399897:TCT:T,NC_000019.10:40399897:TCT:TCTCT,NC_000019.10:40399897:TCT:TCTCTCTCT
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCT=0./0 (ALFA)
TC=0.00005/3 (GnomAD)
TCTCTC=0.03373/130 (ALSPAC)
TCTCTC=0.03425/127 (TWINSUK)
HGVS:: NC_000019.10:g.40399899_40399900del, NC_000019.10:g.40399899_40399900dup, NC_000019.10:g.40399899CT[4], NC_000019.9:g.40905806_40905807del, NC_000019.9:g.40905806_40905807dup, NC_000019.9:g.40905806CT[4], NG_007979.1:g.18466_18467del, NG_007979.1:g.18466_18467dup, NG_007979.1:g.18466GA[4]

Select item 149144620410.

rs1491446204 has merged into rs1405040159 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 19:40399891 (GRCh38)
19:40905798 (GRCh37)
Canonical SPDI:: NC_000019.10:40399889:TCT:T,NC_000019.10:40399889:TCT:TCTCT
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCT=0./0 (ALFA)
HGVS:: NC_000019.10:g.40399891_40399892del, NC_000019.10:g.40399891_40399892dup, NC_000019.9:g.40905798_40905799del, NC_000019.9:g.40905798_40905799dup, NG_007979.1:g.18474_18475del, NG_007979.1:g.18474_18475dup

Select item 149144382811.

rs1491443828 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 19:40399867 (GRCh38)
19:40905774 (GRCh37)
Canonical SPDI:: NC_000019.10:40399865:TCT:T
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.40399867_40399868del, NC_000019.9:g.40905774_40905775del, NG_007979.1:g.18498_18499del

Select item 149142315812.

rs1491423158 has merged into rs1331941769 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 19:40399883 (GRCh38)
19:40905790 (GRCh37)
Canonical SPDI:: NC_000019.10:40399881:TCT:T,NC_000019.10:40399881:TCT:TCTCT
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TCTCT=0./0 (ALFA)
TC=0.00002/1 (GnomAD)
HGVS:: NC_000019.10:g.40399883_40399884del, NC_000019.10:g.40399883_40399884dup, NC_000019.9:g.40905790_40905791del, NC_000019.9:g.40905790_40905791dup, NG_007979.1:g.18482_18483del, NG_007979.1:g.18482_18483dup

Select item 149138520013.

rs1491385200 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ACCCAGC,C [Show Flanks]
Chromosome:: 19:40399870 (GRCh38)
19:40905778 (GRCh37)
Canonical SPDI:: NC_000019.10:40399870:C:CACCCAGC,NC_000019.10:40399870:C:CC
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
HGVS:: NC_000019.10:g.40399871_40399872insACCCAGC, NC_000019.10:g.40399871dup, NC_000019.9:g.40905778_40905779insACCCAGC, NC_000019.9:g.40905778dup, NG_007979.1:g.18494_18495insCTGGGTG, NG_007979.1:g.18494dup

Select item 149135861514.

rs1491358615 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 19:40399887 (GRCh38)
19:40905794 (GRCh37)
Canonical SPDI:: NC_000019.10:40399885:TCT:T,NC_000019.10:40399885:TCT:TCTCT
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCT=0./0 (ALFA)
HGVS:: NC_000019.10:g.40399887_40399888del, NC_000019.10:g.40399887_40399888dup, NC_000019.9:g.40905794_40905795del, NC_000019.9:g.40905794_40905795dup, NG_007979.1:g.18478_18479del, NG_007979.1:g.18478_18479dup

Select item 149132793415.

rs1491327934 has merged into rs1428784507 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT [Show Flanks]
Chromosome:: 19:40399871 (GRCh38)
19:40905778 (GRCh37)
Canonical SPDI:: NC_000019.10:40399869:TCT:T,NC_000019.10:40399869:TCT:TCTCT
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TCTCT=0./0 (ALFA)
TC=0.00002/1 (GnomAD)
HGVS:: NC_000019.10:g.40399871_40399872del, NC_000019.10:g.40399871_40399872dup, NC_000019.9:g.40905778_40905779del, NC_000019.9:g.40905778_40905779dup, NG_007979.1:g.18494_18495del, NG_007979.1:g.18494_18495dup

Select item 149128835516.

rs1491288355 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTTC [Show Flanks]
Chromosome:: 19:40399880 (GRCh38)
19:40905788 (GRCh37)
Canonical SPDI:: NC_000019.10:40399880:TTC:TTCCTTC
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTCCTTC=0.00008/1 (ALFA)
TTCC=0.00003/2 (GnomAD)
HGVS:: NC_000019.10:g.40399883_40399884insCTTC, NC_000019.9:g.40905790_40905791insCTTC, NG_007979.1:g.18484_18485insGGAA

Select item 149128715717.

rs1491287157 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTT,CTTTCTT,CTTTCTTTCTT,CTTTCTTTCTTTCTT [Show Flanks]
Chromosome:: 19:40399904 (GRCh38)
19:40905812 (GRCh37)
Canonical SPDI:: NC_000019.10:40399904:TT:TTCTT,NC_000019.10:40399904:TT:TTCTTTCTT,NC_000019.10:40399904:TT:TTCTTTCTTTCTT,NC_000019.10:40399904:TT:TTCTTTCTTTCTTTCTT
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTCTTTCTTTCTT=0./0 (ALFA)
TTC=0.00032/7 (TOMMO)
HGVS:: NC_000019.10:g.40399906_40399907insCTT, NC_000019.10:g.40399905_40399906TTCT[2]T[1], NC_000019.10:g.40399905_40399906TTCT[3]T[1], NC_000019.10:g.40399905_40399906TTCT[4]T[1], NC_000019.9:g.40905813_40905814insCTT, NC_000019.9:g.40905812_40905813TTCT[2]T[1], NC_000019.9:g.40905812_40905813TTCT[3]T[1], NC_000019.9:g.40905812_40905813TTCT[4]T[1], NG_007979.1:g.18460_18461insGAA, NG_007979.1:g.18459_18460AAGA[2]A[1], NG_007979.1:g.18459_18460AAGA[3]A[1], NG_007979.1:g.18459_18460AAGA[4]A[1]

Select item 149126213318.

rs1491262133 has merged into rs71171569 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 19:40400602 (GRCh38)
19:40906509 (GRCh37)
Canonical SPDI:: NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:40400592:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000019.10:g.40400602_40400618del, NC_000019.10:g.40400604_40400618del, NC_000019.10:g.40400606_40400618del, NC_000019.10:g.40400607_40400618del, NC_000019.10:g.40400608_40400618del, NC_000019.10:g.40400609_40400618del, NC_000019.10:g.40400610_40400618del, NC_000019.10:g.40400611_40400618del, NC_000019.10:g.40400612_40400618del, NC_000019.10:g.40400613_40400618del, NC_000019.10:g.40400614_40400618del, NC_000019.10:g.40400615_40400618del, NC_000019.10:g.40400616_40400618del, NC_000019.10:g.40400617_40400618del, NC_000019.10:g.40400618del, NC_000019.10:g.40400618dup, NC_000019.10:g.40400617_40400618dup, NC_000019.10:g.40400616_40400618dup, NC_000019.10:g.40400615_40400618dup, NC_000019.10:g.40400614_40400618dup, NC_000019.10:g.40400613_40400618dup, NC_000019.10:g.40400612_40400618dup, NC_000019.10:g.40400611_40400618dup, NC_000019.10:g.40400610_40400618dup, NC_000019.10:g.40400609_40400618dup, NC_000019.10:g.40400608_40400618dup, NC_000019.10:g.40400607_40400618dup, NC_000019.10:g.40400606_40400618dup, NC_000019.10:g.40400605_40400618dup, NC_000019.10:g.40400604_40400618dup, NC_000019.10:g.40400598_40400618dup, NC_000019.10:g.40400597_40400618dup, NC_000019.10:g.40400596_40400618dup, NC_000019.10:g.40400595_40400618dup, NC_000019.10:g.40400594_40400618dup, NC_000019.10:g.40400593_40400618dup, NC_000019.10:g.40400618_40400619insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.10:g.40400618_40400619insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.10:g.40400618_40400619insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.10:g.40400618_40400619insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.10:g.40400618_40400619insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.10:g.40400618_40400619insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.10:g.40400618_40400619insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.10:g.40400618_40400619insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.10:g.40400618_40400619insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.40906509_40906525del, NC_000019.9:g.40906511_40906525del, NC_000019.9:g.40906513_40906525del, NC_000019.9:g.40906514_40906525del, NC_000019.9:g.40906515_40906525del, NC_000019.9:g.40906516_40906525del, NC_000019.9:g.40906517_40906525del, NC_000019.9:g.40906518_40906525del, NC_000019.9:g.40906519_40906525del, NC_000019.9:g.40906520_40906525del, NC_000019.9:g.40906521_40906525del, NC_000019.9:g.40906522_40906525del, NC_000019.9:g.40906523_40906525del, NC_000019.9:g.40906524_40906525del, NC_000019.9:g.40906525del, NC_000019.9:g.40906525dup, NC_000019.9:g.40906524_40906525dup, NC_000019.9:g.40906523_40906525dup, NC_000019.9:g.40906522_40906525dup, NC_000019.9:g.40906521_40906525dup, NC_000019.9:g.40906520_40906525dup, NC_000019.9:g.40906519_40906525dup, NC_000019.9:g.40906518_40906525dup, NC_000019.9:g.40906517_40906525dup, NC_000019.9:g.40906516_40906525dup, NC_000019.9:g.40906515_40906525dup, NC_000019.9:g.40906514_40906525dup, NC_000019.9:g.40906513_40906525dup, NC_000019.9:g.40906512_40906525dup, NC_000019.9:g.40906511_40906525dup, NC_000019.9:g.40906505_40906525dup, NC_000019.9:g.40906504_40906525dup, NC_000019.9:g.40906503_40906525dup, NC_000019.9:g.40906502_40906525dup, NC_000019.9:g.40906501_40906525dup, NC_000019.9:g.40906500_40906525dup, NC_000019.9:g.40906525_40906526insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.40906525_40906526insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.40906525_40906526insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.40906525_40906526insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.40906525_40906526insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.40906525_40906526insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.40906525_40906526insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.40906525_40906526insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.40906525_40906526insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_007979.1:g.17756_17772del, NG_007979.1:g.17758_17772del, NG_007979.1:g.17760_17772del, NG_007979.1:g.17761_17772del, NG_007979.1:g.17762_17772del, NG_007979.1:g.17763_17772del, NG_007979.1:g.17764_17772del, NG_007979.1:g.17765_17772del, NG_007979.1:g.17766_17772del, NG_007979.1:g.17767_17772del, NG_007979.1:g.17768_17772del, NG_007979.1:g.17769_17772del, NG_007979.1:g.17770_17772del, NG_007979.1:g.17771_17772del, NG_007979.1:g.17772del, NG_007979.1:g.17772dup, NG_007979.1:g.17771_17772dup, NG_007979.1:g.17770_17772dup, NG_007979.1:g.17769_17772dup, NG_007979.1:g.17768_17772dup, NG_007979.1:g.17767_17772dup, NG_007979.1:g.17766_17772dup, NG_007979.1:g.17765_17772dup, NG_007979.1:g.17764_17772dup, NG_007979.1:g.17763_17772dup, NG_007979.1:g.17762_17772dup, NG_007979.1:g.17761_17772dup, NG_007979.1:g.17760_17772dup, NG_007979.1:g.17759_17772dup, NG_007979.1:g.17758_17772dup, NG_007979.1:g.17752_17772dup, NG_007979.1:g.17751_17772dup, NG_007979.1:g.17750_17772dup, NG_007979.1:g.17749_17772dup, NG_007979.1:g.17748_17772dup, NG_007979.1:g.17747_17772dup, NG_007979.1:g.17772_17773insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_007979.1:g.17772_17773insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_007979.1:g.17772_17773insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_007979.1:g.17772_17773insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_007979.1:g.17772_17773insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_007979.1:g.17772_17773insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_007979.1:g.17772_17773insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_007979.1:g.17772_17773insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_007979.1:g.17772_17773insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149120006019.

rs1491200060 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTTTCTTTCTTTC [Show Flanks]
Chromosome:: 19:40399886 (GRCh38)
19:40905794 (GRCh37)
Canonical SPDI:: NC_000019.10:40399886:CTTTCTTTCTTTC:CTTTCTTTCTTTCCTTTCTTTCTTTC
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CTTTCTTTCTTTCCTTTCTTTCTTTC=0./0 (ALFA)
HGVS:: NC_000019.10:g.40399887_40399899dup, NC_000019.9:g.40905794_40905806dup, NG_007979.1:g.18466_18478dup

Select item 149119685020.

rs1491196850 has merged into rs1207479189 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,TTT [Show Flanks]
Chromosome:: 19:40399881 (GRCh38)
19:40905788 (GRCh37)
Canonical SPDI:: NC_000019.10:40399879:TTT:T,NC_000019.10:40399879:TTT:TTTT
Gene:: PRX (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTT=0./0 (ALFA)
T=0.00002/1 (GnomAD)
HGVS:: NC_000019.10:g.40399881_40399882del, NC_000019.10:g.40399882dup, NC_000019.9:g.40905788_40905789del, NC_000019.9:g.40905789dup, NG_007979.1:g.18484_18485del, NG_007979.1:g.18485dup

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