236348415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12557075-C-T

http://identifiers.org/hco/1/GRCh38#236348427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12557066-C-A

236348427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12557066-C-T

http://identifiers.org/hco/1/GRCh38#236348630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12556903-C-A

236348630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12556903-C-G

236348630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12556903-C-T

236348704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12556859-G-A

236348704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12556859-G-T

236348708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12556855-C-T

236353665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12555040-G-A

236353667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12555038-G-A

236353749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12554949-G-A

236353766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12554934-T-C

236353991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12554814-C-T

236354002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12554803-A-G

236354021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12554786-C-T

236354157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12554646-T-G

236389552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron_variant, undefined
orthologous variants: 12545200-T-G

http://identifiers.org/hco/1/GRCh38#236390684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12543193-C-A

236390869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12543015-G-T

236394191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12536717-T-C

http://identifiers.org/hco/1/GRCh38#236394192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12536716-C-A

http://identifiers.org/hco/1/GRCh38#236394193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12536715-C-A

236394324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 12536605-C-T

236394493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron_variant, missense_variant
orthologous variants: 12536512-G-A

236394504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 12536501-G-A

236394504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 12536501-G-C

236394506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 12536499-G-A

236394506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 12536499-G-C

236394512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 12536493-A-G

236394517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12536488-T-A

236394586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12536430-G-T

http://identifiers.org/hco/1/GRCh38#236394598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12536418-A-C

236394612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12536404-T-A

236394612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12536404-T-C

236394612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12536404-T-G

236394640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12536165-T-A

236394909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12535498-T-C

236395148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12535260-G-A

236395148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12535260-G-C

236395151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron_variant, undefined
orthologous variants: 12535257-C-T

http://identifiers.org/hco/1/GRCh38#236395234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#12535181-C-A

236395234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron_variant, undefined
orthologous variants: 12535181-C-T

236395378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: intron variant
orthologous variants: 12535062-G-A

236395439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 12535017-T-C

236395489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 12534959-G-A

236395489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 12534959-G-C

236395489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 12534959-G-T

http://identifiers.org/hco/1/GRCh38#236395492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12534956-C-A

236395492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 12534956-C-T

http://identifiers.org/hco/1/GRCh38#236395553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12534904-C-A

236395553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 12534904-C-T

http://identifiers.org/hco/1/GRCh38#236395598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#12534859-C-A

236395598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 12534859-C-T

236395612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 12534845-T-C

236395642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 12534815-G-A

236395642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 12534815-G-T

236395665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12534792-A-G

236395665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12534792-A-T

236395746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12534743-A-G

http://identifiers.org/hco/1/GRCh38#236395761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12534720-C-A

236395761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12534720-C-G

236395761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12534720-C-T

236395831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 12534532-C-G

236395864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 12534482-C-T

http://identifiers.org/hco/1/GRCh38#236396425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12533947-C-A

236396500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12533872-T-C

236396717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12533612-A-T

236396867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12533504-C-G

236397044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12533355-T-G

236397053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12533344-C-T

236397060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12533337-G-A

http://identifiers.org/hco/1/GRCh38#236397200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12533072-A-C

236397454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12532712-G-A

236397454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12532712-G-T

236397602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12532599-G-T

236397843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12532370-G-A

236398652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12532033-G-T

236398754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12531965-G-A

236398969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12531749-T-G

236399014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12531702-G-C

236399014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12531702-G-T

236399053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12531665-C-T

236399145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12531433-A-G

236399174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12531403-G-A

236399661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 12530804-G-A

http://identifiers.org/hco/1/GRCh38#236399780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#12530734-A-C

236399951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 12530578-G-T

236401660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12529489-T-C

236401766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12529412-G-C

http://identifiers.org/hco/1/GRCh38#236401820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12529324-C-A

236401820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12529324-C-T

236404464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12526157-C-T

236404565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12526050-A-G

236404584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12526021-G-T

236408125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12523568-G-C

236409173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12523337-A-G

236409173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12523337-A-T

236409431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12523115-A-G

236413869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12522657-A-G

236413869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12522657-A-T

http://identifiers.org/hco/1/GRCh38#236413870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12522656-C-A

236413879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12522648-T-G

236413904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12522627-G-A

http://identifiers.org/hco/1/GRCh38#236414178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12522343-C-A

236414178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12522343-C-T

http://identifiers.org/hco/1/GRCh38#236414221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12522238-C-A

236414221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12522238-C-T

236414320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12522139-T-C

236414423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12522035-G-A

236414423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12522035-G-T

236414498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12522007-A-G

236414762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12521774-A-G

236415015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12521542-C-T

236416234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12519834-G-A

236416305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12519755-G-A

236416305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12519755-G-T

236416812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12519335-A-G

236416830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12519317-A-G

236417049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12518991-G-A

236417053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12518987-G-T

236417061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12518972-G-A

236417163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12518836-A-G

236425126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12516668-G-C

236425185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12516610-C-T

236425191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12516604-C-T

236425244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12516566-G-A

236425285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12516526-C-T

236425358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12516495-G-A

http://identifiers.org/hco/1/GRCh38#236425729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12516194-C-A

236425729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12516194-C-G

236427199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12515671-G-A

236427333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12515547-G-A

236427333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12515547-G-C

236427368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12515515-T-C

236427386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 12515494-T-C

http://identifiers.org/hco/1/GRCh38#236427425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12515455-C-A

236427425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 12515455-C-T

http://identifiers.org/hco/1/GRCh38#236427456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12515424-A-C

236427488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12515395-A-G

236427488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12515395-A-T

236455462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12509714-G-A

236455464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12509712-A-T

236455607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12509573-C-G

236455609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12509571-T-A

236455702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12509496-C-T

http://identifiers.org/hco/1/GRCh38#236456586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12508516-A-C

236456649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12508464-C-T

236456658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12508455-C-T

http://identifiers.org/hco/1/GRCh38#236456719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12508388-C-A

236456720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12508387-C-G

236456735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12508372-C-T

http://identifiers.org/hco/1/GRCh38#236456772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12508342-A-C

236456776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12508338-C-T

236456933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12508211-G-A

236457047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12508120-C-T

236457066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12508102-T-C

236459437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12506757-T-G

236459461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12506738-A-G

236463963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12502888-G-A

236464167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12502792-C-T

236465758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12501278-G-C

236465764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12501272-G-A

236465901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 12501034-A-G

236465952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12500980-G-T

236466102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12500837-A-G

236466464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12500514-C-T

236466597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12500272-G-A

236466618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12500251-C-T

236466644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12500226-C-G

http://identifiers.org/hco/1/GRCh38#236468117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12498650-C-A

236468224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 12498531-T-A

236468224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 12498531-T-C

236468301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12498449-C-G

236468301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12498449-C-T

http://identifiers.org/hco/1/GRCh38#236468306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12498444-C-A

http://identifiers.org/hco/1/GRCh38#236474650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12496426-C-A

http://identifiers.org/hco/1/GRCh38#236474660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12496416-A-C

236474660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12496416-A-G

236480605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12495206-T-C

236480608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12495203-A-G

236480640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12495178-T-A

236480651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12495167-G-A

236482206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12493520-G-A

236482242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12493475-T-C

http://identifiers.org/hco/1/GRCh38#236482282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12493438-A-C

236482282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 12493438-A-G

236482294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 12493426-A-G

236482552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 12493159-G-A

236482566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 12493145-G-A

236482566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 12493145-G-C

236482673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 12493038-C-G

236482809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 12492917-T-G

236482868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 12492858-G-T

http://identifiers.org/hco/1/GRCh38#236483020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12492714-C-A

236483023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 12492707-C-T

http://identifiers.org/hco/1/GRCh38#236483051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12492674-C-A

236483051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 12492674-C-G

http://identifiers.org/hco/1/GRCh38#236484933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12492649-C-A

236484937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12492645-C-G

236486375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12491476-A-G

236486546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12491309-T-C

236486563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12491293-G-A

236489060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12489633-T-G

236489063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12489630-T-G

236489114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12489574-T-C

236489860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12489098-C-G

236489988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12488909-A-G

236489993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12488904-T-C

236490088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 12488837-C-T

236490095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 12488830-T-A

236490970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12488517-A-G

236491125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12488342-T-A

236491164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12488303-C-T

http://identifiers.org/hco/1/GRCh38#236491706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12488043-C-A

236491706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12488043-C-T

236491760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 12487994-C-T

236491770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 12487984-G-T

236491824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 12487930-T-C

http://identifiers.org/hco/1/GRCh38#236491875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12487883-C-A

236491875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12487883-C-T

236491918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12487861-G-T

http://identifiers.org/hco/1/GRCh38#236491952-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12487830-A-C

236492075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 12487742-T-A

236492116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 12487711-T-C

236492119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 12487708-C-T

236492129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 12487698-A-G

236492300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12487543-G-T

236498830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12486082-C-T

236498958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14341
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 12485964-T-C