ClinVar

NM_000572.3(IL10):c.361C>T (p.Leu121=)

Genes:

IL10:interleukin 10 [Gene - OMIM - HGNC]
IL19:interleukin 19 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q32.1

Genomic location:

• Chr1: 206770924 (on Assembly GRCh38)
• Chr1: 206944269 (on Assembly GRCh37)

Preferred name:

NM_000572.3(IL10):c.361C>T (p.Leu121=)

HGVS:

• NC_000001.11:g.206770924G>A
• NG_012088.1:g.6571C>T
• NG_165401.1:g.91G>A
• NM_000572.3:c.361C>TMANE SELECT
• NM_001382624.1:c.106C>T
• NM_001393490.1:c.-149+94G>A
• NM_153758.5:c.-303G>AMANE SELECT
• NP_000563.1:p.Leu121=
• NP_001369553.1:p.Leu36=
• LRG_1230t1:c.361C>T
• LRG_1230:g.6571C>T
• LRG_1230p1:p.Leu121=
• NC_000001.10:g.206944269G>A
• NR_168466.1:n.420C>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_153758.5:c.-303G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001393490.1:c.-149+94G>A - intron variant - [Sequence Ontology: SO:0001627]
• NR_168466.1:n.420C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_000572.3:c.361C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001382624.1:c.106C>T - synonymous variant - [Sequence Ontology: SO:0001819]