Product Details

Primer Sequences

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Primer Chromosome Location

Chr.19: 46494622-46494857 on Build GRCh38 View in UCSC browser

Format

Each primer will be delivered in a single tube, dried-down

Quick Reference Guide

Primer Designer^™ Tool Quick Reference

Ampliseq ID's

Gene Details

Gene Symbol

PNMAL2

Entrez Gene ID

57469

Gene Name

paraneoplastic Ma antigen family-like 2

Gene Aliases

-

UniGene

Hs.7193

Gene Chromosome Location

Chr.19: 46491191-46495912 on Build GRCh38

Transcripts

NM_020709.2 NM_001205281.1

Gene Symbol

PPP5D1

Entrez Gene ID

100506012

Gene Name

PPP5 tetratricopeptide repeat domain containing 1

Gene Aliases

-

UniGene

Hs.671661

Gene Chromosome Location

Chr.19: 46480788-46601200 on Build GRCh38

Transcripts

NM_020709.2 NM_001205281.1

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
998439	c.160G>A	p.A54T	Chr.19: 46494792-46494792 on Build GRCh38
7285300	c.676A>G	p.T226A	Chr.19: 46494790-46494790 on Build GRCh38
5744193	c.677C>T	p.T226M	Chr.19: 46494789-46494789 on Build GRCh38
1394780	c.81G>A	p.S27S	Chr.19: 46494713-46494713 on Build GRCh38
1612443	c.118G>A	p.A40T	Chr.19: 46494750-46494750 on Build GRCh38
7257967	c.734+2delG	p.?	Chr.19: 46494730-46494730 on Build GRCh38
6574238	c.777C>T	p.V259V	Chr.19: 46494689-46494689 on Build GRCh38
1612446	c.128T>A	p.L43Q	Chr.19: 46494760-46494760 on Build GRCh38
263023	c.45C>T	p.F15F	Chr.19: 46494677-46494677 on Build GRCh38
5856221	c.707G>A	p.R236K	Chr.19: 46494759-46494759 on Build GRCh38
401865	c.46G>A	p.D16N	Chr.19: 46494678-46494678 on Build GRCh38
5921563	c.728C>T	p.S243F	Chr.19: 46494738-46494738 on Build GRCh38
5032463	c.839T>G	p.L280W	Chr.19: 46494627-46494627 on Build GRCh38
5744192	c.677C>T	p.T226M	Chr.19: 46494789-46494789 on Build GRCh38
4965600	c.646G>A	p.G216R	Chr.19: 46494820-46494820 on Build GRCh38
7257968	c.98delC	p.S35fs*9	Chr.19: 46494730-46494730 on Build GRCh38
5856222	c.707G>A	p.R236K	Chr.19: 46494759-46494759 on Build GRCh38
4965602	c.188C>T	p.P63L	Chr.19: 46494820-46494820 on Build GRCh38
6751357	c.714G>T	p.W238C	Chr.19: 46494752-46494752 on Build GRCh38
998438	c.674C>T	p.A225V	Chr.19: 46494792-46494792 on Build GRCh38
7285301	c.158T>C	p.V53A	Chr.19: 46494790-46494790 on Build GRCh38
3389154	c.80C>T	p.S27L	Chr.19: 46494712-46494712 on Build GRCh38
6751358	c.714G>T	p.W238C	Chr.19: 46494752-46494752 on Build GRCh38
7257966	c.736delG	p.E246fs*35	Chr.19: 46494730-46494730 on Build GRCh38
3404410	c.60G>A	p.T20T	Chr.19: 46494692-46494692 on Build GRCh38
6574239	c.57G>A	p.V19V	Chr.19: 46494689-46494689 on Build GRCh38
3389153	c.754G>A	p.E252K	Chr.19: 46494712-46494712 on Build GRCh38
3404409	c.774C>T	p.T258T	Chr.19: 46494692-46494692 on Build GRCh38
4965601	c.646G>A	p.G216R	Chr.19: 46494820-46494820 on Build GRCh38
1481253	c.835C>T	p.R279C	Chr.19: 46494631-46494631 on Build GRCh38
6751359	c.120C>A	p.A40A	Chr.19: 46494752-46494752 on Build GRCh38
1612442	c.716C>T	p.A239V	Chr.19: 46494750-46494750 on Build GRCh38
1394779	c.753C>T	p.R251R	Chr.19: 46494713-46494713 on Build GRCh38
1612445	c.706A>T	p.R236W	Chr.19: 46494760-46494760 on Build GRCh38
5921562	c.728C>T	p.S243F	Chr.19: 46494738-46494738 on Build GRCh38
5744194	c.157G>A	p.V53M	Chr.19: 46494789-46494789 on Build GRCh38
5856223	c.127C>T	p.L43L	Chr.19: 46494759-46494759 on Build GRCh38
5921564	c.106G>A	p.E36K	Chr.19: 46494738-46494738 on Build GRCh38
1612441	c.716C>T	p.A239V	Chr.19: 46494750-46494750 on Build GRCh38
1612444	c.706A>T	p.R236W	Chr.19: 46494760-46494760 on Build GRCh38
7285299	c.676A>G	p.T226A	Chr.19: 46494790-46494790 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs967991080	Chr.19: 46494801-46494801 on Build GRCh38
rs771224713	Chr.19: 46494717-46494717 on Build GRCh38
rs919978202	Chr.19: 46494800-46494800 on Build GRCh38
rs754635701	Chr.19: 46494678-46494678 on Build GRCh38
rs767184857	Chr.19: 46494826-46494826 on Build GRCh38
rs772337171	Chr.19: 46494748-46494748 on Build GRCh38
rs780606470	Chr.19: 46494686-46494686 on Build GRCh38
rs146376571	Chr.19: 46494774-46494774 on Build GRCh38
rs760855001	Chr.19: 46494759-46494759 on Build GRCh38
rs375528723	Chr.19: 46494728-46494728 on Build GRCh38
rs762932360	Chr.19: 46494778-46494778 on Build GRCh38
rs751190548	Chr.19: 46494677-46494677 on Build GRCh38
rs758269236	Chr.19: 46494642-46494642 on Build GRCh38
rs775495148	Chr.19: 46494756-46494756 on Build GRCh38
rs138594215	Chr.19: 46494715-46494715 on Build GRCh38
rs1025320269	Chr.19: 46494707-46494707 on Build GRCh38
rs751337008	Chr.19: 46494812-46494812 on Build GRCh38
rs764199146	Chr.19: 46494766-46494766 on Build GRCh38
rs142336941	Chr.19: 46494721-46494721 on Build GRCh38
rs1032034744	Chr.19: 46494670-46494670 on Build GRCh38
rs143805999	Chr.19: 46494647-46494647 on Build GRCh38
rs766133213	Chr.19: 46494789-46494789 on Build GRCh38
rs139093853	Chr.19: 46494836-46494836 on Build GRCh38
rs35793066	Chr.19: 46494677-46494678 on Build GRCh38
rs372340134	Chr.19: 46494714-46494714 on Build GRCh38
rs752288047	Chr.19: 46494829-46494829 on Build GRCh38
rs754651152	Chr.19: 46494820-46494820 on Build GRCh38
rs747653196	Chr.19: 46494688-46494688 on Build GRCh38
rs1022186470	Chr.19: 46494781-46494781 on Build GRCh38
rs1012007352	Chr.19: 46494702-46494702 on Build GRCh38

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