Variant #0000304812 (NC_000001.10:g.247978306G>T, NM_012353.2:c.-56598C>A (OR1C1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.247978306G>T
DNA change (hg38) g.247815004G>T
Published as OR14A16(NM_001001966.1):c.726C>A (p.H242Q)
ISCN -
DB-ID OR14A16_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR11L1 NM_001001959.1 ?/. - c.*25924C>A r.(=) p.(=)
OR14A16 NM_001001966.1 ?/. - c.726C>A r.(?) p.(His242Gln)
OR6F1 NM_001005286.1 ?/. - c.-102249C>A r.(?) p.(=)
OR13G1 NM_001005487.1 ?/. - c.-141963C>A r.(?) p.(=)
OR1C1 NM_012353.2 ?/. - c.-56598C>A r.(?) p.(=)
TRIM58 NM_015431.3 ?/. - c.-42243G>T r.(?) p.(=)


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