ClinVar

NM_006979.3(SLC39A7):c.471C>T (p.Pro157=)

Gene:

SLC39A7:solute carrier family 39 member 7 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p21.32

Genomic location:

• Chr6: 33201804 (on Assembly GRCh38)
• Chr6: 33169581 (on Assembly GRCh37)

Preferred name:

NM_006979.3(SLC39A7):c.471C>T (p.Pro157=)

HGVS:

• NC_000006.12:g.33201804C>T
• NG_023374.1:g.3852G>A
• NM_001077516.2:c.471C>T
• NM_001288777.2:c.96C>T
• NM_006979.3:c.471C>TMANE SELECT
• NP_001070984.1:p.Pro157=
• NP_001275706.1:p.Pro32=
• NP_008910.2:p.Pro157=
• NC_000006.11:g.33169581C>T
• NC_000006.11:g.33169581C>T
• NM_001077516.1:c.471C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs11538810

NCBI 1000 Genomes Browser:

rs11538810

Molecular consequence:

• NM_001077516.2:c.471C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001288777.2:c.96C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_006979.3:c.471C>T - synonymous variant - [Sequence Ontology: SO:0001819]