Variant #0000332923 (NC_000009.11:g.139734943A>C, NM_024718.4:c.2159A>C (RABL6))

Chromosome 9
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.139734943A>C
DNA change (hg38) g.136840491A>C
Published as RABL6(NM_001173988.1):c.2162A>C (p.(His721Pro))
ISCN -
DB-ID RABL6_000007
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
C9orf172 NM_001080482.2 -?/. - c.-3924A>C r.(?) p.(=)
RABL6 NM_024718.4 -?/. - c.2159A>C r.(?) p.(His720Pro)


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