ClinVar

NM_022168.4(IFIH1):c.906G>A (p.Pro302=)

Gene:

IFIH1:interferon induced with helicase C domain 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q24.2

Genomic location:

• Chr2: 162288324 (on Assembly GRCh38)
• Chr2: 163144834 (on Assembly GRCh37)

Preferred name:

NM_022168.4(IFIH1):c.906G>A (p.Pro302=)

HGVS:

• NC_000002.12:g.162288324C>T
• NG_011495.1:g.35206G>A
• NM_022168.4:c.906G>AMANE SELECT
• NP_071451.2:p.Pro302=
• LRG_1235t1:c.906G>A
• LRG_1235:g.35206G>A
• LRG_1235p1:p.Pro302=
• NC_000002.11:g.163144834C>T
• NC_000002.11:g.163144834C>T
• NM_022168.3:c.906G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs775441863

NCBI 1000 Genomes Browser:

rs775441863

Molecular consequence:

• NM_022168.4:c.906G>A - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

2