SNP Links for Gene (Select 283922) - SNP

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Select item 14915464351.

rs1491546435 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 16:74365940 (GRCh38)
16:74399838 (GRCh37)
Canonical SPDI:: NC_000016.10:74365939:AT:
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000008/1 (GnomAD)
HGVS:: NC_000016.10:g.74365940_74365941del, NC_000016.9:g.74399838_74399839del

Select item 14915159552.

rs1491515955 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 16:74345077 (GRCh38)
16:74378975 (GRCh37)
Canonical SPDI:: NC_000016.10:74345076:AT:
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000008/1 (GnomAD)
HGVS:: NC_000016.10:g.74345077_74345078del, NC_000016.9:g.74378975_74378976del

Select item 14915159223.

rs1491515922 has merged into rs1555529189 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATATATAT>-,AT,ATAT,ATATAT,ATATATATAT,ATATATATATAT,ATATATATATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT,ATATATATATATATATATATAT,ATATATATATATATATATATATAT,ATATATATATATATATATATATATAT,ATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATAT [Show Flanks]
Chromosome:: 16:74355746 (GRCh38)
16:74389644 (GRCh37)
Canonical SPDI:: NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATAT,NC_000016.10:74355732:TATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATATATATATAT
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATATATAT=0./0 (ALFA)
HGVS:: NC_000016.10:g.74355734AT[6], NC_000016.10:g.74355734AT[7], NC_000016.10:g.74355734AT[8], NC_000016.10:g.74355734AT[9], NC_000016.10:g.74355734AT[11], NC_000016.10:g.74355734AT[12], NC_000016.10:g.74355734AT[13], NC_000016.10:g.74355734AT[14], NC_000016.10:g.74355734AT[15], NC_000016.10:g.74355734AT[16], NC_000016.10:g.74355734AT[17], NC_000016.10:g.74355734AT[18], NC_000016.10:g.74355734AT[19], NC_000016.10:g.74355734AT[20], NC_000016.10:g.74355734AT[21], NC_000016.10:g.74355734AT[22], NC_000016.10:g.74355734AT[23], NC_000016.9:g.74389632AT[6], NC_000016.9:g.74389632AT[7], NC_000016.9:g.74389632AT[8], NC_000016.9:g.74389632AT[9], NC_000016.9:g.74389632AT[11], NC_000016.9:g.74389632AT[12], NC_000016.9:g.74389632AT[13], NC_000016.9:g.74389632AT[14], NC_000016.9:g.74389632AT[15], NC_000016.9:g.74389632AT[16], NC_000016.9:g.74389632AT[17], NC_000016.9:g.74389632AT[18], NC_000016.9:g.74389632AT[19], NC_000016.9:g.74389632AT[20], NC_000016.9:g.74389632AT[21], NC_000016.9:g.74389632AT[22], NC_000016.9:g.74389632AT[23]

Select item 14914639034.

rs1491463903 [Homo sapiens]

Variant type:: INS
Alleles:: ->GTAC [Show Flanks]
Chromosome:: 16:74355733 (GRCh38)
16:74389632 (GRCh37)
Canonical SPDI:: NC_000016.10:74355733::GTAC
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GTAC=0./0 (ALFA)
GTAC=0.00014/8 (GnomAD)
HGVS:: NC_000016.10:g.74355733_74355734insGTAC, NC_000016.9:g.74389631_74389632insGTAC

Select item 14914505235.

rs1491450523 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GT [Show Flanks]
Chromosome:: 16:74355670 (GRCh38)
16:74389569 (GRCh37)
Canonical SPDI:: NC_000016.10:74355670:TGTGTGT:TGTGTGTGT
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGT=0.000169/2 (ALFA)
TG=0./0 (Korea1K)
TG=0.000195/24 (GnomAD)
HGVS:: NC_000016.10:g.74355672GT[4], NC_000016.9:g.74389570GT[4]

Select item 14914329066.

rs1491432906 has merged into rs1171157001 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 16:74355760 (GRCh38)
16:74389658 (GRCh37)
Canonical SPDI:: NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000016.10:74355752:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTT=0./0 (ALFA)
HGVS:: NC_000016.10:g.74355760_74355769del, NC_000016.10:g.74355761_74355769del, NC_000016.10:g.74355762_74355769del, NC_000016.10:g.74355763_74355769del, NC_000016.10:g.74355764_74355769del, NC_000016.10:g.74355765_74355769del, NC_000016.10:g.74355766_74355769del, NC_000016.10:g.74355767_74355769del, NC_000016.10:g.74355768_74355769del, NC_000016.10:g.74355769del, NC_000016.10:g.74355769dup, NC_000016.10:g.74355768_74355769dup, NC_000016.10:g.74355767_74355769dup, NC_000016.10:g.74355766_74355769dup, NC_000016.10:g.74355765_74355769dup, NC_000016.9:g.74389658_74389667del, NC_000016.9:g.74389659_74389667del, NC_000016.9:g.74389660_74389667del, NC_000016.9:g.74389661_74389667del, NC_000016.9:g.74389662_74389667del, NC_000016.9:g.74389663_74389667del, NC_000016.9:g.74389664_74389667del, NC_000016.9:g.74389665_74389667del, NC_000016.9:g.74389666_74389667del, NC_000016.9:g.74389667del, NC_000016.9:g.74389667dup, NC_000016.9:g.74389666_74389667dup, NC_000016.9:g.74389665_74389667dup, NC_000016.9:g.74389664_74389667dup, NC_000016.9:g.74389663_74389667dup

Select item 14913576487.

rs1491357648 [Homo sapiens]

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

Select item 14912695678.

rs1491269567 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATA,ATATA,ATATATA,ATATATATA,ATATATATATA,ATATATATATATA,ATATATATATATATA,ATATATATATATATATA,ATATATATATATATATATA,ATATATATATATATATATATA,ATATATATATATATATATATATA,ATATATATATATATATATATATATA [Show Flanks]
Chromosome:: 16:74355753 (GRCh38)
16:74389652 (GRCh37)
Canonical SPDI:: NC_000016.10:74355753::A,NC_000016.10:74355753::ATA,NC_000016.10:74355753::ATATA,NC_000016.10:74355753::ATATATA,NC_000016.10:74355753::ATATATATA,NC_000016.10:74355753::ATATATATATA,NC_000016.10:74355753::ATATATATATATA,NC_000016.10:74355753::ATATATATATATATA,NC_000016.10:74355753::ATATATATATATATATA,NC_000016.10:74355753::ATATATATATATATATATA,NC_000016.10:74355753::ATATATATATATATATATATA,NC_000016.10:74355753::ATATATATATATATATATATATA,NC_000016.10:74355753::ATATATATATATATATATATATATA
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATA=0./0 (ALFA)
HGVS:: NC_000016.10:g.74355753_74355754insA, NC_000016.10:g.74355753_74355754insATA, NC_000016.10:g.74355753_74355754insATATA, NC_000016.10:g.74355753_74355754insATATATA, NC_000016.10:g.74355753_74355754insATATATATA, NC_000016.10:g.74355753_74355754insATATATATATA, NC_000016.10:g.74355753_74355754insATATATATATATA, NC_000016.10:g.74355753_74355754insATATATATATATATA, NC_000016.10:g.74355753_74355754insATATATATATATATATA, NC_000016.10:g.74355753_74355754insATATATATATATATATATA, NC_000016.10:g.74355753_74355754insATATATATATATATATATATA, NC_000016.10:g.74355753_74355754insATATATATATATATATATATATA, NC_000016.10:g.74355753_74355754insATATATATATATATATATATATATA, NC_000016.9:g.74389651_74389652insA, NC_000016.9:g.74389651_74389652insATA, NC_000016.9:g.74389651_74389652insATATA, NC_000016.9:g.74389651_74389652insATATATA, NC_000016.9:g.74389651_74389652insATATATATA, NC_000016.9:g.74389651_74389652insATATATATATA, NC_000016.9:g.74389651_74389652insATATATATATATA, NC_000016.9:g.74389651_74389652insATATATATATATATA, NC_000016.9:g.74389651_74389652insATATATATATATATATA, NC_000016.9:g.74389651_74389652insATATATATATATATATATA, NC_000016.9:g.74389651_74389652insATATATATATATATATATATA, NC_000016.9:g.74389651_74389652insATATATATATATATATATATATA, NC_000016.9:g.74389651_74389652insATATATATATATATATATATATATA

Select item 14912548509.

rs1491254850 has merged into rs35591542 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 16:74345090 (GRCh38)
16:74378988 (GRCh37)
Canonical SPDI:: NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000016.10:g.74345090_74345095del, NC_000016.10:g.74345092_74345095del, NC_000016.10:g.74345093_74345095del, NC_000016.10:g.74345094_74345095del, NC_000016.10:g.74345095del, NC_000016.10:g.74345095dup, NC_000016.10:g.74345094_74345095dup, NC_000016.10:g.74345093_74345095dup, NC_000016.10:g.74345090_74345095dup, NC_000016.10:g.74345087_74345095dup, NC_000016.9:g.74378988_74378993del, NC_000016.9:g.74378990_74378993del, NC_000016.9:g.74378991_74378993del, NC_000016.9:g.74378992_74378993del, NC_000016.9:g.74378993del, NC_000016.9:g.74378993dup, NC_000016.9:g.74378992_74378993dup, NC_000016.9:g.74378991_74378993dup, NC_000016.9:g.74378988_74378993dup, NC_000016.9:g.74378985_74378993dup

Select item 149123448910.

rs1491234489 has merged into rs1196431061 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTT>-,T,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT [Show Flanks]
Chromosome:: 16:74365951 (GRCh38)
16:74399849 (GRCh37)
Canonical SPDI:: NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000016.10:74365940:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000016.10:g.74365951_74365957del, NC_000016.10:g.74365952_74365957del, NC_000016.10:g.74365955_74365957del, NC_000016.10:g.74365956_74365957del, NC_000016.10:g.74365957del, NC_000016.10:g.74365957dup, NC_000016.10:g.74365956_74365957dup, NC_000016.10:g.74365955_74365957dup, NC_000016.9:g.74399849_74399855del, NC_000016.9:g.74399850_74399855del, NC_000016.9:g.74399853_74399855del, NC_000016.9:g.74399854_74399855del, NC_000016.9:g.74399855del, NC_000016.9:g.74399855dup, NC_000016.9:g.74399854_74399855dup, NC_000016.9:g.74399853_74399855dup

Select item 149121598111.

rs1491215981 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 16:74355670 (GRCh38)
16:74389568 (GRCh37)
Canonical SPDI:: NC_000016.10:74355669:AT:
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00018/3 (ALFA)
-=0.00026/4 (TOMMO)
-=0.00043/31 (GnomAD)
HGVS:: NC_000016.10:g.74355670_74355671del, NC_000016.9:g.74389568_74389569del

Select item 149120409512.

rs1491204095 has merged into rs35591542 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 16:74345090 (GRCh38)
16:74378988 (GRCh37)
Canonical SPDI:: NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:74345077:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000016.10:g.74345090_74345095del, NC_000016.10:g.74345092_74345095del, NC_000016.10:g.74345093_74345095del, NC_000016.10:g.74345094_74345095del, NC_000016.10:g.74345095del, NC_000016.10:g.74345095dup, NC_000016.10:g.74345094_74345095dup, NC_000016.10:g.74345093_74345095dup, NC_000016.10:g.74345090_74345095dup, NC_000016.10:g.74345087_74345095dup, NC_000016.9:g.74378988_74378993del, NC_000016.9:g.74378990_74378993del, NC_000016.9:g.74378991_74378993del, NC_000016.9:g.74378992_74378993del, NC_000016.9:g.74378993del, NC_000016.9:g.74378993dup, NC_000016.9:g.74378992_74378993dup, NC_000016.9:g.74378991_74378993dup, NC_000016.9:g.74378988_74378993dup, NC_000016.9:g.74378985_74378993dup

Select item 149115451813.

rs1491154518 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 16:74369138 (GRCh38)
16:74403036 (GRCh37)
Canonical SPDI:: NC_000016.10:74369137:AT:
Gene:: PDPR2P (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000337/4 (ALFA)
-=0.000541/75 (GnomAD)
HGVS:: NC_000016.10:g.74369138_74369139del, NC_000016.9:g.74403036_74403037del

Select item 149115287914.

rs1491152879 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,AA [Show Flanks]
Chromosome:: 16:74359327 (GRCh38)
16:74393226 (GRCh37)
Canonical SPDI:: NC_000016.10:74359327::A,NC_000016.10:74359327::AA
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
A=0.0019/53 (TOMMO)
HGVS:: NC_000016.10:g.74359327_74359328insA, NC_000016.10:g.74359327_74359328insAA, NC_000016.9:g.74393225_74393226insA, NC_000016.9:g.74393225_74393226insAA

Select item 149099090115.

rs1490990901 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:74335767 (GRCh38)
16:74369665 (GRCh37)
Canonical SPDI:: NC_000016.10:74335766:C:A
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000224/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000546/1 (Korea1K)
HGVS:: NC_000016.10:g.74335767C>A, NC_000016.9:g.74369665C>A

Select item 149097672816.

rs1490976728 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:74337390 (GRCh38)
16:74371288 (GRCh37)
Canonical SPDI:: NC_000016.10:74337389:G:A
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.74337390G>A, NC_000016.9:g.74371288G>A

Select item 149095100817.

rs1490951008 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:74361182 (GRCh38)
16:74395080 (GRCh37)
Canonical SPDI:: NC_000016.10:74361181:G:T
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.74361182G>T, NC_000016.9:g.74395080G>T

Select item 149092460718.

rs1490924607 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:74361741 (GRCh38)
16:74395639 (GRCh37)
Canonical SPDI:: NC_000016.10:74361740:T:C
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000016.10:g.74361741T>C, NC_000016.9:g.74395639T>C

Select item 149085283219.

rs1490852832 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACG>- [Show Flanks]
Chromosome:: 16:74336611 (GRCh38)
16:74370509 (GRCh37)
Canonical SPDI:: NC_000016.10:74336609:GACG:G
Gene:: PDPR2P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.74336611_74336613del, NC_000016.9:g.74370509_74370511del, NR_026950.1:n.1953_1955del

Select item 149082120820.

rs1490821208 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 16:74367847 (GRCh38)
16:74401745 (GRCh37)
Canonical SPDI:: NC_000016.10:74367846:G:A,NC_000016.10:74367846:G:C
Gene:: PDPR2P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000016.10:g.74367847G>A, NC_000016.10:g.74367847G>C, NC_000016.9:g.74401745G>A, NC_000016.9:g.74401745G>C

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