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See other NHSL1 GT Assays ›
SNP ID:
rs9495201
Gene
NHSL1
Gene Name
Set Membership:
-
Chromosome Location:
Chr.6: 138677231 - 138677231 on Build GRCh38
Polymorphism:
A/G, Transition substitution
Context Sequence [VIC/FAM]:

CCTATGTCTGCCTCAAGTTTTCCTA[A/G]TTACATTTTTTAGGAGGCATTCTAA

Assay ID C__29496261_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

Literature Links:

 NHSL1 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global - Not Available Caucasian - Not Available CEPH (CEU) - Not Available
EAS - Not Available African American - Not Available YRI (Yoruba) - Not Available
SAS - Not Available Chinese - Not Available CHB (Han Chinese) - Not Available
AFR - Not Available Japanese - Not Available JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
NHSL1 - NHS like 1
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001144060.1 Intron NP_001137532.1
NM_020464.1 Intron NP_065197.1
XM_005267062.4 Intron XP_005267119.1
XM_011535965.2 Intron XP_011534267.1
XM_011535966.2 Intron XP_011534268.1
XM_011535967.2 Intron XP_011534269.1
XM_011535968.2 Intron XP_011534270.1
XM_011535969.2 Intron XP_011534271.1
XM_011535970.2 Intron XP_011534272.1
XM_011535971.2 Intron XP_011534273.1
XM_011535972.2 Intron XP_011534274.1
XM_011535973.2 Intron XP_011534275.1
XM_011535974.2 Intron XP_011534276.1
XM_011535976.1 Intron XP_011534278.1
XM_017011086.1 Intron XP_016866575.1
XM_017011087.1 Intron XP_016866576.1
XM_017011088.1 Intron XP_016866577.1
XM_017011089.1 Intron XP_016866578.1

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