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TGGGCCTGGAATGTAGACTAATGGT[A/G]AGCATACAGATTTGTTTTTAATTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 400028 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NLGN4Y PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
NLGN4Y - neuroligin 4, Y-linked | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164238.1 | Intron | NP_001157710.1 | ||||
NM_001206850.1 | Intron | NP_001193779.1 | ||||
NM_014893.4 | Intron | NP_055708.3 | ||||
XM_006724874.2 | Intron | XP_006724937.1 | ||||
XM_011531424.2 | Intron | XP_011529726.1 | ||||
XM_011531425.2 | Intron | XP_011529727.1 | ||||
XM_011531426.2 | Intron | XP_011529728.1 | ||||
XM_011531427.1 | Intron | XP_011529729.1 | ||||
XM_011531428.1 | Intron | XP_011529730.1 | ||||
XM_011531429.2 | Intron | XP_011529731.1 | ||||
XM_011531430.2 | Intron | XP_011529732.1 | ||||
XM_017030034.1 | Intron | XP_016885523.1 | ||||
XM_017030035.1 | Intron | XP_016885524.1 | ||||
XM_017030036.1 | Intron | XP_016885525.1 | ||||
XM_017030037.1 | Intron | XP_016885526.1 | ||||
XM_017030038.1 | Intron | XP_016885527.1 | ||||
XM_017030039.1 | Intron | XP_016885528.1 | ||||
XM_017030040.1 | Intron | XP_016885529.1 | ||||
XM_017030041.1 | Intron | XP_016885530.1 |