ClinVar

NM_001320.7(CSNK2B):c.107T>C (p.Leu36Pro)

Gene:

CSNK2B:casein kinase 2 beta [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p21.33

Genomic location:

• Chr6: 31667902 (on Assembly GRCh38)
• Chr6: 31635679 (on Assembly GRCh37)

Preferred name:

NM_001320.7(CSNK2B):c.107T>C (p.Leu36Pro)

HGVS:

• NC_000006.12:g.31667902T>C
• NM_001282385.2:c.107T>C
• NM_001320.7:c.107T>CMANE SELECT
• NP_001269314.1:p.Leu36Pro
• NP_001311.3:p.Leu36Pro
• NC_000006.11:g.31635679T>C
• NM_001320.5:c.107T>C

This HGVS expression did not pass validation

Protein change:

L36P

Links:

dbSNP: rs2151185393

NCBI 1000 Genomes Browser:

rs2151185393

Molecular consequence:

• NM_001282385.2:c.107T>C - missense variant - [Sequence Ontology: SO:0001583]
• NM_001320.7:c.107T>C - missense variant - [Sequence Ontology: SO:0001583]