Variant #0000281490 (NC_000002.11:g.27693802G>C, NM_015662.1:c.1685C>G (IFT172))

Chromosome 2
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.27693802G>C
DNA change (hg38) g.27470935G>C
Published as IFT172(NM_015662.1):c.1685C>G (p.(Thr562Ser)), IFT172(NM_015662.2):c.1685C>G (p.T562S), IFT172(NM_015662.3):c.1685C>G (p.T562S)
ISCN -
DB-ID IFT172_000018 See all 5 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) 0.00652 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFT172 NM_015662.1 -?/. - c.1685C>G r.(?) p.(Thr562Ser)


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