Variant #0000976798 (NC_000005.9:g.38493836G>T, NM_002310.5:c.1937C>A (LIFR))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38493836G>T
DNA change (hg38) -
Published as LIFR(NM_001127671.1):c.1937C>A (p.(Thr646Asn)), LIFR(NM_001127671.2):c.1937C>A (p.T646N), LIFR(NM_002310.6):c.1937C>A (p.T646N)
ISCN -
DB-ID LIFR_000027 See all 3 reported entries
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) 0.00201 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LIFR NM_002310.5 -?/. - c.1937C>A r.(?) p.(Thr646Asn)


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