INSL4 c.82C>G ;(p.L28V)

Variant ID: 9-5231605-C-G

NM_002195.1(INSL4):c.82C>G;(p.L28V)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Whole-genome sequencing in multiplex families with psychoses reveals mutations in the SHANK2 and SMARCA1 genes segregating with illness.

Molecular Psychiatry
Homann, O R OR; Misura, K K; Lamas, E E; Sandrock, R W RW; Nelson, P P; McDonough, S I SI; DeLisi, L E LE
Publication Date: 2016-12

Variant appearance in text: INSL4: L28V; rs146584562
PubMed Link: 27001614
Variant Present in the following documents:
  • NIHMS753666-supplement-2.xlsx, sheet 10
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