SNP Links for Protein (Select 27894300) - SNP

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:112913845 (GRCh38)
2:113671422 (GRCh37)
Canonical SPDI:: NC_000002.12:112913844:G:T
Gene:: IL37 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,missense_variant,upstream_transcript_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.112913845G>T, NC_000002.11:g.113671422G>T, NG_029219.1:g.5875G>T, NM_014439.4:c.136G>T, NM_014439.3:c.136G>T, NM_173204.2:c.136G>T, NM_173204.1:c.136G>T, NP_055254.2:p.Val46Phe, NP_775296.1:p.Val46Phe

Select item 140337075211.

rs1403370752 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 2:112913830 (GRCh38)
2:113671407 (GRCh37)
Canonical SPDI:: NC_000002.12:112913829:C:A
Gene:: IL37 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.112913830C>A, NC_000002.11:g.113671407C>A, NG_029219.1:g.5860C>A, NM_014439.4:c.121C>A, NM_014439.3:c.121C>A, NM_173204.2:c.121C>A, NM_173204.1:c.121C>A, NP_055254.2:p.Pro41Thr, NP_775296.1:p.Pro41Thr

Select item 139573924312.

rs1395739243 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:112913829 (GRCh38)
2:113671406 (GRCh37)
Canonical SPDI:: NC_000002.12:112913828:C:T
Gene:: IL37 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.112913829C>T, NC_000002.11:g.113671406C>T, NG_029219.1:g.5859C>T, NM_014439.4:c.120C>T, NM_014439.3:c.120C>T, NM_173204.2:c.120C>T, NM_173204.1:c.120C>T

Select item 138703485713.

rs1387034857 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:112917675 (GRCh38)
2:113675252 (GRCh37)
Canonical SPDI:: NC_000002.12:112917674:T:C
Gene:: IL37 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000057/2 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000002.12:g.112917675T>C, NC_000002.11:g.113675252T>C, NG_029219.1:g.9705T>C, NM_014439.4:c.306T>C, NM_014439.3:c.306T>C, NM_173202.2:c.243T>C, NM_173202.1:c.243T>C, NM_173204.2:c.186T>C, NM_173204.1:c.186T>C, NM_173203.2:c.123T>C, NM_173203.1:c.123T>C, NM_173205.2:c.228T>C, NM_173205.1:c.228T>C

Select item 138601295514.

rs1386012955 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:112918609 (GRCh38)
2:113676186 (GRCh37)
Canonical SPDI:: NC_000002.12:112918608:C:T
Gene:: IL37 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.112918609C>T, NC_000002.11:g.113676186C>T, NG_029219.1:g.10639C>T, NM_014439.4:c.457C>T, NM_014439.3:c.457C>T, NM_173202.2:c.394C>T, NM_173202.1:c.394C>T, NM_173204.2:c.337C>T, NM_173204.1:c.337C>T, NM_173203.2:c.274C>T, NM_173203.1:c.274C>T, NM_173205.2:c.379C>T, NM_173205.1:c.379C>T, NP_055254.2:p.Pro153Ser, NP_775294.1:p.Pro132Ser, NP_775296.1:p.Pro113Ser, NP_775295.1:p.Pro92Ser, NP_775297.1:p.Pro127Ser

Select item 138410600615.

rs1384106006 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:112917710 (GRCh38)
2:113675287 (GRCh37)
Canonical SPDI:: NC_000002.12:112917709:C:T
Gene:: IL37 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.112917710C>T, NC_000002.11:g.113675287C>T, NG_029219.1:g.9740C>T, NM_014439.4:c.341C>T, NM_014439.3:c.341C>T, NM_173202.2:c.278C>T, NM_173202.1:c.278C>T, NM_173204.2:c.221C>T, NM_173204.1:c.221C>T, NM_173203.2:c.158C>T, NM_173203.1:c.158C>T, NM_173205.2:c.263C>T, NM_173205.1:c.263C>T, NP_055254.2:p.Ser114Phe, NP_775294.1:p.Ser93Phe, NP_775296.1:p.Ser74Phe, NP_775295.1:p.Ser53Phe, NP_775297.1:p.Ser88Phe

Select item 137969098716.

rs1379690987 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 2:112913805 (GRCh38)
2:113671382 (GRCh37)
Canonical SPDI:: NC_000002.12:112913804:C:A,NC_000002.12:112913804:C:G
Gene:: IL37 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.112913805C>A, NC_000002.12:g.112913805C>G, NC_000002.11:g.113671382C>A, NC_000002.11:g.113671382C>G, NG_029219.1:g.5835C>A, NG_029219.1:g.5835C>G, NM_014439.4:c.96C>A, NM_014439.4:c.96C>G, NM_014439.3:c.96C>A, NM_014439.3:c.96C>G, NM_173204.2:c.96C>A, NM_173204.2:c.96C>G, NM_173204.1:c.96C>A, NM_173204.1:c.96C>G, NP_055254.2:p.Ser32Arg, NP_055254.2:p.Ser32Arg, NP_775296.1:p.Ser32Arg, NP_775296.1:p.Ser32Arg

Select item 137148426517.

rs1371484265 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 2:112913813 (GRCh38)
2:113671390 (GRCh37)
Canonical SPDI:: NC_000002.12:112913812:A:T
Gene:: IL37 (Varview)
Functional Consequence:: missense_variant,upstream_transcript_variant,coding_sequence_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000011/3 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000002.12:g.112913813A>T, NC_000002.11:g.113671390A>T, NG_029219.1:g.5843A>T, NM_014439.4:c.104A>T, NM_014439.3:c.104A>T, NM_173204.2:c.104A>T, NM_173204.1:c.104A>T, NP_055254.2:p.Glu35Val, NP_775296.1:p.Glu35Val

Select item 136889912718.

rs1368899127 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:112918740 (GRCh38)
2:113676317 (GRCh37)
Canonical SPDI:: NC_000002.12:112918739:G:T
Gene:: IL37 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000002.12:g.112918740G>T, NC_000002.11:g.113676317G>T, NG_029219.1:g.10770G>T, NM_014439.4:c.588G>T, NM_014439.3:c.588G>T, NM_173202.2:c.525G>T, NM_173202.1:c.525G>T, NM_173204.2:c.468G>T, NM_173204.1:c.468G>T, NM_173203.2:c.405G>T, NM_173203.1:c.405G>T, NM_173205.2:c.510G>T, NM_173205.1:c.510G>T, NP_055254.2:p.Arg196Ser, NP_775294.1:p.Arg175Ser, NP_775296.1:p.Arg156Ser, NP_775295.1:p.Arg135Ser, NP_775297.1:p.Arg170Ser

Select item 136454478119.

rs1364544781 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:112918728 (GRCh38)
2:113676305 (GRCh37)
Canonical SPDI:: NC_000002.12:112918727:A:G
Gene:: IL37 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.112918728A>G, NC_000002.11:g.113676305A>G, NG_029219.1:g.10758A>G, NM_014439.4:c.576A>G, NM_014439.3:c.576A>G, NM_173202.2:c.513A>G, NM_173202.1:c.513A>G, NM_173204.2:c.456A>G, NM_173204.1:c.456A>G, NM_173203.2:c.393A>G, NM_173203.1:c.393A>G, NM_173205.2:c.498A>G, NM_173205.1:c.498A>G

Select item 136189345720.

rs1361893457 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:112917646 (GRCh38)
2:113675223 (GRCh37)
Canonical SPDI:: NC_000002.12:112917645:G:T
Gene:: IL37 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000009/2 (GnomAD_exomes)
HGVS:: NC_000002.12:g.112917646G>T, NC_000002.11:g.113675223G>T, NG_029219.1:g.9676G>T, NM_014439.4:c.277G>T, NM_014439.3:c.277G>T, NM_173202.2:c.214G>T, NM_173202.1:c.214G>T, NM_173204.2:c.157G>T, NM_173204.1:c.157G>T, NM_173203.2:c.94G>T, NM_173203.1:c.94G>T, NM_173205.2:c.199G>T, NM_173205.1:c.199G>T, NP_055254.2:p.Ala93Ser, NP_775294.1:p.Ala72Ser, NP_775296.1:p.Ala53Ser, NP_775295.1:p.Ala32Ser, NP_775297.1:p.Ala67Ser

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