94683749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 5 prime UTR variant
orthologous variants: 38965048-A-T

94683771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 5 prime UTR variant
orthologous variants: 38965069-G-A

94683771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 5 prime UTR variant
orthologous variants: 38965069-G-C

94683874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38965172-C-T

94683921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: synonymous variant
orthologous variants: 38965219-T-A

94683925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38965223-C-G

94683967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38965265-A-G

94683970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38965268-A-G

94687460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38999178-G-A

94687487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38999204-T-C

94687564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38999278-C-T

94687592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38999320-T-C

94687649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38967309-A-G

http://identifiers.org/hco/10/GRCh38#94687651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38967311-C-A

94687706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38967363-A-G

94687706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38967363-A-T

94687733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38967388-G-A

94687744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38967412-A-G

94687751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38967419-C-T

94687755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38967429-C-G

94687784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: synonymous variant
orthologous variants: 38967459-T-C

94687896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38967571-A-G

94687964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38967632-A-T

94687966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38967634-G-A

http://identifiers.org/hco/10/GRCh38#94688015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38967656-C-A

94688082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38967715-T-G

94688113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38967743-C-T

http://identifiers.org/hco/10/GRCh38#94688166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38967796-C-A

94688166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38967796-C-T

94688175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38967805-C-G

94688175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38967805-C-T

http://identifiers.org/hco/10/GRCh38#94688214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38967842-A-C

94688224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38967852-G-A

94688224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38967852-G-T

94688477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38967930-G-A

94688645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38968047-T-C

94688771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38968151-G-A

http://identifiers.org/hco/10/GRCh38#94688853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38968226-C-A

94688853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38968226-C-T

94688929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38968296-A-G

94688976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38968341-G-A

94688976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38968341-G-C

94689062-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38968425-T-A

94689062-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38968425-T-G

94689864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38968971-A-G

94689986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38969089-C-G

94693626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38969445-C-G

94694228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38970761-G-A

http://identifiers.org/hco/10/GRCh38#94694233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38970766-C-A

94694286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38970817-T-C

94694374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38971524-A-G

94694458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38971618-A-G

94694877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38973141-T-A

94694910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 38973176-C-T

http://identifiers.org/hco/10/GRCh38#94694991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38973257-C-A

94694991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: stop gained
orthologous variants: 38973257-C-T

94695054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38973320-A-G

http://identifiers.org/hco/10/GRCh38#94695064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38973330-C-A

94695064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38973330-C-T

http://identifiers.org/hco/10/GRCh38#94695083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38973349-A-C

94695083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38973349-A-G

94695083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38973349-A-T

94705572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38974576-T-A

94705578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38974582-T-A

94705677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38974672-T-G

94705857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38974829-C-T

94706088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38975269-G-A

94706154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38975367-A-G

94706181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38975389-G-A

94706181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38975389-G-C

94706181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38975389-G-T

http://identifiers.org/hco/10/GRCh38#94706585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38975754-C-A

94706585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38975754-C-T

http://identifiers.org/hco/10/GRCh38#94706714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38976488-C-A

94706714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38976488-C-T

http://identifiers.org/hco/10/GRCh38#94706731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38976499-C-A

94706731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38976499-C-T

94706750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38976507-T-G

94706761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38976518-A-G

94706770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38976527-T-A

94706810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38976567-C-T

94706811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron_variant, missense_variant
orthologous variants: 38976568-G-A

94706811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron_variant, missense_variant
orthologous variants: 38976568-G-T

94706833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron_variant, missense_variant
orthologous variants: 38976590-A-G

94706889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron_variant, stop_gained
orthologous variants: 38976649-G-T

http://identifiers.org/hco/10/GRCh38#94706892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38976652-C-A

http://identifiers.org/hco/10/GRCh38#94706904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38976664-C-A

94706904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron_variant, missense_variant
orthologous variants: 38976664-C-G

94706955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron_variant, missense_variant
orthologous variants: 38976715-G-A

94706955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron_variant, missense_variant
orthologous variants: 38976715-G-C

94706966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38976726-A-G

94707013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38976992-A-G

http://identifiers.org/hco/10/GRCh38#94707041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38977020-C-A

94707060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977039-G-A

94707060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977039-G-T

94707083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977062-G-A

94707083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977062-G-C

94707083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977062-G-T

94707090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977069-G-A

94707090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977069-G-C

94707090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977069-G-T

http://identifiers.org/hco/10/GRCh38#94707102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38977081-A-C

94707102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977081-A-G

94707102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977081-A-T

94707377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977345-A-G

94707390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977357-C-G

94707482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977427-C-T

http://identifiers.org/hco/10/GRCh38#94707652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38977587-C-A

94707746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977688-C-T

94707805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977746-A-G

94707808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977747-C-T

94707907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38977821-T-C

94708114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38978486-G-A

http://identifiers.org/hco/10/GRCh38#94708136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38978503-C-A

94708136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38978503-C-T

94708171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38978521-C-T

94708280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38978625-A-G

94708436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38978698-C-T

94708454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38978718-G-A

94708511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38978775-T-C

94720204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 39022482-G-T

http://identifiers.org/hco/10/GRCh38#94720275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38983743-C-A

94720275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38983743-C-G

94720275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38983743-C-T

94720507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: synonymous variant
orthologous variants: 38983965-C-T

94720531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38983989-G-A

94720680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38984127-T-C

http://identifiers.org/hco/10/GRCh38#94720764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38984209-A-C

94723803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 39023191-G-A

94723803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 39023191-G-C

94724124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38986673-C-T

94724190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38986736-A-G

http://identifiers.org/hco/10/GRCh38#94724205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38986739-C-A

94724205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38986739-C-T

94724245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38986773-T-C

94724265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38986793-T-C

94724273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38986801-T-C

94724273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38986801-T-G

http://identifiers.org/hco/10/GRCh38#94724322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38986851-C-A

94724322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38986851-C-G

94724322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38986851-C-T

94724336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38986864-G-C

94724336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38986864-G-T

http://identifiers.org/hco/10/GRCh38#94724393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38986921-C-A

94724393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38986921-C-T

94724403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38986931-A-G

94724458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: synonymous variant
orthologous variants: 38986975-C-T

http://identifiers.org/hco/10/GRCh38#94724463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38986980-A-C

94724463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38986980-A-G

94724465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38986982-C-T

http://identifiers.org/hco/10/GRCh38#94724467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38986984-C-A

94724467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: synonymous variant
orthologous variants: 38986984-C-G

94724467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: synonymous variant
orthologous variants: 38986984-C-T

94724476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: synonymous variant
orthologous variants: 38986993-C-T

94724561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38987074-T-A

94728561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38988912-A-G

94728583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38988933-C-T

http://identifiers.org/hco/10/GRCh38#94728584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38988934-C-A

94728584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38988934-C-T

94728611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38988961-A-G

http://identifiers.org/hco/10/GRCh38#94728630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38988981-C-A

94728630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38988981-C-T

94728660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989008-T-C

94728661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989009-A-G

94728689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989037-T-A

94728692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989040-G-A

94728692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989040-G-T

94728700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989048-T-C

http://identifiers.org/hco/10/GRCh38#94728735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38989084-C-A

94728735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989084-C-T

http://identifiers.org/hco/10/GRCh38#94728739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38989088-C-A

94728739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989088-C-T

94733023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 39078840-C-T

94733072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 39078850-T-C

94733147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989464-C-T

94733224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989537-T-C

94733317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: synonymous variant
orthologous variants: 38989607-C-T

http://identifiers.org/hco/10/GRCh38#94733334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38989624-A-C

94733390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38989680-A-G

94733399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38989689-A-T

94733401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: synonymous variant
orthologous variants: 38989691-C-T

94733415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38989705-A-G

94733431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38989721-C-G

94733463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989753-T-A

http://identifiers.org/hco/10/GRCh38#94733494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38989784-C-A

94733531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989823-C-T

94733543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989834-G-A

94733543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989834-G-T

94733585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989878-G-A

94733585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38989878-G-T

94733717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38990546-G-A

94733845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38990654-G-A

94733845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38990654-G-T

94734034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38990826-G-A

94734053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38990844-T-G

94734061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38990854-G-A

http://identifiers.org/hco/10/GRCh38#94734371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38991149-A-C

94734371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38991149-A-G

94734495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38991266-C-G

94734747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 39027996-A-G

94734761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 39028010-G-A

94734767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 39028016-T-C

http://identifiers.org/hco/10/GRCh38#94735148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#39030351-C-A

94735148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 39030351-C-T

http://identifiers.org/hco/10/GRCh38#94735224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38991499-A-C

94735240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38991515-T-A

http://identifiers.org/hco/10/GRCh38#94735246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38991526-A-C

94735246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: intron variant
orthologous variants: 38991526-A-G

94735268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38991556-C-G

94735268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38991556-C-T

94735292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38991580-G-A

94735292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38991580-G-T

94735295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38991583-C-G

94735295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38991583-C-T

94735320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: missense variant
orthologous variants: 38991608-C-T

94735420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: synonymous variant
orthologous variants: 38991708-C-T

94735450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: 38991735-G-A

94735450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: 38991735-G-T

94735469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: 38991744-C-T

94735611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: 38991871-G-A

94735634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: 38991894-A-G

http://identifiers.org/hco/10/GRCh38#94735722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38991992-C-A

94735759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: 38992026-T-C

94735759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: 38992026-T-G

http://identifiers.org/hco/10/GRCh38#94735777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38992044-C-A

94735777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: 38992044-C-T

94735813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: 38992073-G-A

94735813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: 38992073-G-T

94736139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2620
most severe consequence: 3 prime UTR variant
orthologous variants: 39082836-C-G