Variant #0000610363 (NC_000006.11:g.43270008A>G, NM_206922.2:c.*3544T>C (CRIP3))

Chromosome 6
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.43270008A>G
DNA change (hg38) g.43302270A>G
Published as SLC22A7(NM_153320.2):c.1132A>G (p.T378A)
ISCN -
DB-ID CRIP3_000002
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +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     
SLC22A7 NM_006672.3 ?/. - c.1126A>G r.(?) p.(Thr376Ala)
CRIP3 NM_206922.2 ?/. - c.*3544T>C r.(=) p.(=)


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