SNP Links for Protein (Select 281427286) - SNP

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Links from Protein

Items: 1 to 20 of 457

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Select item 14900744321.

rs1490074432 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:83524003 (GRCh38)
6:84233722 (GRCh37)
Canonical SPDI:: NC_000006.12:83524002:T:C
Gene:: PRSS35 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.83524003T>C, NC_000006.11:g.84233722T>C, NM_153362.3:c.562T>C, NM_153362.2:c.562T>C, NM_001170423.2:c.562T>C, NM_001170423.1:c.562T>C

Select item 14849354312.

rs1484935431 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:83524677 (GRCh38)
6:84234396 (GRCh37)
Canonical SPDI:: NC_000006.12:83524676:C:T
Gene:: PRSS35 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000006.12:g.83524677C>T, NC_000006.11:g.84234396C>T, NM_153362.3:c.1236C>T, NM_153362.2:c.1236C>T, NM_001170423.2:c.1236C>T, NM_001170423.1:c.1236C>T

Select item 14829723373.

rs1482972337 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:83524098 (GRCh38)
6:84233817 (GRCh37)
Canonical SPDI:: NC_000006.12:83524097:C:T
Gene:: PRSS35 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000006.12:g.83524098C>T, NC_000006.11:g.84233817C>T, NM_153362.3:c.657C>T, NM_153362.2:c.657C>T, NM_001170423.2:c.657C>T, NM_001170423.1:c.657C>T

Select item 14815347804.

rs1481534780 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:83523494 (GRCh38)
6:84233213 (GRCh37)
Canonical SPDI:: NC_000006.12:83523493:T:C
Gene:: PRSS35 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.83523494T>C, NC_000006.11:g.84233213T>C, NM_153362.3:c.53T>C, NM_153362.2:c.53T>C, NM_001170423.2:c.53T>C, NM_001170423.1:c.53T>C, NP_699193.2:p.Ile18Thr, NP_001163894.1:p.Ile18Thr

Select item 14805707145.

rs1480570714 [Homo sapiens]

Variant type:: DEL
Alleles:: TTCCCCTCAGCATGTTCTAACTG>- [Show Flanks]
Chromosome:: 6:83523918 (GRCh38)
6:84233637 (GRCh37)
Canonical SPDI:: NC_000006.12:83523917:TTCCCCTCAGCATGTTCTAACTG:
Gene:: PRSS35 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.83523918_83523940del, NC_000006.11:g.84233637_84233659del, NM_153362.3:c.477_499del, NM_153362.2:c.477_499del, NM_001170423.2:c.477_499del, NM_001170423.1:c.477_499del, NP_699193.2:p.Ser160fs, NP_001163894.1:p.Ser160fs

Select item 14791079796.

rs1479107979 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:83523776 (GRCh38)
6:84233495 (GRCh37)
Canonical SPDI:: NC_000006.12:83523775:C:A
Gene:: PRSS35 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000006.12:g.83523776C>A, NC_000006.11:g.84233495C>A, NM_153362.3:c.335C>A, NM_153362.2:c.335C>A, NM_001170423.2:c.335C>A, NM_001170423.1:c.335C>A, NP_699193.2:p.Thr112Asn, NP_001163894.1:p.Thr112Asn

Select item 14775814277.

rs1477581427 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 6:83523576 (GRCh38)
6:84233295 (GRCh37)
Canonical SPDI:: NC_000006.12:83523575:C:
Gene:: PRSS35 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.83523576del, NC_000006.11:g.84233295del, NM_153362.3:c.135del, NM_153362.2:c.135del, NM_001170423.2:c.135del, NM_001170423.1:c.135del, NP_699193.2:p.Thr46fs, NP_001163894.1:p.Thr46fs

Select item 14740097478.

rs1474009747 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:83524408 (GRCh38)
6:84234127 (GRCh37)
Canonical SPDI:: NC_000006.12:83524407:C:T
Gene:: PRSS35 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000006.12:g.83524408C>T, NC_000006.11:g.84234127C>T, NM_153362.3:c.967C>T, NM_153362.2:c.967C>T, NM_001170423.2:c.967C>T, NM_001170423.1:c.967C>T, NP_699193.2:p.Arg323Trp, NP_001163894.1:p.Arg323Trp

Select item 14699493989.

rs1469949398 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:83524489 (GRCh38)
6:84234208 (GRCh37)
Canonical SPDI:: NC_000006.12:83524488:G:T
Gene:: PRSS35 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000006.12:g.83524489G>T, NC_000006.11:g.84234208G>T, NM_153362.3:c.1048G>T, NM_153362.2:c.1048G>T, NM_001170423.2:c.1048G>T, NM_001170423.1:c.1048G>T, NP_699193.2:p.Val350Phe, NP_001163894.1:p.Val350Phe

Select item 146841375210.

rs1468413752 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 6:83524181 (GRCh38)
6:84233901 (GRCh37)
Canonical SPDI:: NC_000006.12:83524181:TT:TTT
Gene:: PRSS35 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.83524183dup, NC_000006.11:g.84233902dup, NM_153362.3:c.742dup, NM_153362.2:c.742dup, NM_001170423.2:c.742dup, NM_001170423.1:c.742dup, NP_699193.2:p.Ser248fs, NP_001163894.1:p.Ser248fs

Select item 146838666711.

rs1468386667 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:83524024 (GRCh38)
6:84233743 (GRCh37)
Canonical SPDI:: NC_000006.12:83524023:A:G
Gene:: PRSS35 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000006.12:g.83524024A>G, NC_000006.11:g.84233743A>G, NM_153362.3:c.583A>G, NM_153362.2:c.583A>G, NM_001170423.2:c.583A>G, NM_001170423.1:c.583A>G, NP_699193.2:p.Ser195Gly, NP_001163894.1:p.Ser195Gly

Select item 146787943812.

rs1467879438 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:83524305 (GRCh38)
6:84234024 (GRCh37)
Canonical SPDI:: NC_000006.12:83524304:G:T
Gene:: PRSS35 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.83524305G>T, NC_000006.11:g.84234024G>T, NM_153362.3:c.864G>T, NM_153362.2:c.864G>T, NM_001170423.2:c.864G>T, NM_001170423.1:c.864G>T, NP_699193.2:p.Lys288Asn, NP_001163894.1:p.Lys288Asn

Select item 146683415513.

rs1466834155 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:83523801 (GRCh38)
6:84233520 (GRCh37)
Canonical SPDI:: NC_000006.12:83523800:A:G
Gene:: PRSS35 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.83523801A>G, NC_000006.11:g.84233520A>G, NM_153362.3:c.360A>G, NM_153362.2:c.360A>G, NM_001170423.2:c.360A>G, NM_001170423.1:c.360A>G

Select item 146527910814.

rs1465279108 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:83524312 (GRCh38)
6:84234031 (GRCh37)
Canonical SPDI:: NC_000006.12:83524311:A:G
Gene:: PRSS35 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000029/4 (GnomAD)
HGVS:: NC_000006.12:g.83524312A>G, NC_000006.11:g.84234031A>G, NM_153362.3:c.871A>G, NM_153362.2:c.871A>G, NM_001170423.2:c.871A>G, NM_001170423.1:c.871A>G, NP_699193.2:p.Met291Val, NP_001163894.1:p.Met291Val

Select item 146182691615.

rs1461826916 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:83524633 (GRCh38)
6:84234352 (GRCh37)
Canonical SPDI:: NC_000006.12:83524632:C:G
Gene:: PRSS35 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.83524633C>G, NC_000006.11:g.84234352C>G, NM_153362.3:c.1192C>G, NM_153362.2:c.1192C>G, NM_001170423.2:c.1192C>G, NM_001170423.1:c.1192C>G, NP_699193.2:p.Gln398Glu, NP_001163894.1:p.Gln398Glu

Select item 146026919616.

rs1460269196 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:83524334 (GRCh38)
6:84234053 (GRCh37)
Canonical SPDI:: NC_000006.12:83524333:C:T
Gene:: PRSS35 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.83524334C>T, NC_000006.11:g.84234053C>T, NM_153362.3:c.893C>T, NM_153362.2:c.893C>T, NM_001170423.2:c.893C>T, NM_001170423.1:c.893C>T, NP_699193.2:p.Thr298Met, NP_001163894.1:p.Thr298Met

Select item 145704873317.

rs1457048733 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 6:83523727 (GRCh38)
6:84233446 (GRCh37)
Canonical SPDI:: NC_000006.12:83523726:A:C
Gene:: PRSS35 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000006.12:g.83523727A>C, NC_000006.11:g.84233446A>C, NM_153362.3:c.286A>C, NM_153362.2:c.286A>C, NM_001170423.2:c.286A>C, NM_001170423.1:c.286A>C, NP_699193.2:p.Thr96Pro, NP_001163894.1:p.Thr96Pro

Select item 145250923518.

rs1452509235 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 6:83524532 (GRCh38)
6:84234251 (GRCh37)
Canonical SPDI:: NC_000006.12:83524531:G:A,NC_000006.12:83524531:G:T
Gene:: PRSS35 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
T=0.000035/1 (TOMMO)
HGVS:: NC_000006.12:g.83524532G>A, NC_000006.12:g.83524532G>T, NC_000006.11:g.84234251G>A, NC_000006.11:g.84234251G>T, NM_153362.3:c.1091G>A, NM_153362.3:c.1091G>T, NM_153362.2:c.1091G>A, NM_153362.2:c.1091G>T, NM_001170423.2:c.1091G>A, NM_001170423.2:c.1091G>T, NM_001170423.1:c.1091G>A, NM_001170423.1:c.1091G>T, NP_699193.2:p.Arg364His, NP_699193.2:p.Arg364Leu, NP_001163894.1:p.Arg364His, NP_001163894.1:p.Arg364Leu

Select item 145041953019.

rs1450419530 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:83524601 (GRCh38)
6:84234320 (GRCh37)
Canonical SPDI:: NC_000006.12:83524600:T:C
Gene:: PRSS35 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000019/5 (TOPMED)
C=0.000029/4 (GnomAD)
HGVS:: NC_000006.12:g.83524601T>C, NC_000006.11:g.84234320T>C, NM_153362.3:c.1160T>C, NM_153362.2:c.1160T>C, NM_001170423.2:c.1160T>C, NM_001170423.1:c.1160T>C, NP_699193.2:p.Val387Ala, NP_001163894.1:p.Val387Ala

Select item 145033916120.

rs1450339161 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:83523647 (GRCh38)
6:84233366 (GRCh37)
Canonical SPDI:: NC_000006.12:83523646:A:G
Gene:: PRSS35 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000006.12:g.83523647A>G, NC_000006.11:g.84233366A>G, NM_153362.3:c.206A>G, NM_153362.2:c.206A>G, NM_001170423.2:c.206A>G, NM_001170423.1:c.206A>G, NP_699193.2:p.Glu69Gly, NP_001163894.1:p.Glu69Gly

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