186587931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45505143-T-C

186588201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45504884-A-G

186588201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45504884-A-T

186588335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45504713-T-G

http://identifiers.org/hco/4/GRCh38#186588484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45504562-A-C

186588533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45504508-G-A

186588533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 45504508-G-T

186588650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45504386-C-T

186588765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45504271-C-T

186588830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45504206-C-T

186588876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45504160-G-A

186588876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45504160-G-C

186589305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45503735-A-G

186589305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45503735-A-T

186589338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45503702-G-T

http://identifiers.org/hco/4/GRCh38#186589342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45503698-A-C

186589485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45503605-C-T

186590016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45503203-C-T

186590119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45503126-A-G

186590265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45503012-G-A

186590265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45503012-G-T

186590462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45502811-A-G

186590693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 45502635-A-T

http://identifiers.org/hco/4/GRCh38#186590736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45502594-C-A

http://identifiers.org/hco/4/GRCh38#186590793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45502537-C-A

186590793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45502537-C-G

186590832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45502501-G-A

186590833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45502500-C-T

186591694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45501607-A-G

186592776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45500661-T-C

http://identifiers.org/hco/4/GRCh38#186592809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45500629-A-C

http://identifiers.org/hco/4/GRCh38#186593473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45500107-C-A

186593473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45500107-C-T

186593605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499978-T-C

186593606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499977-G-A

186593606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499977-G-C

186593606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499977-G-T

186593762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499838-C-T

186593882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499723-C-T

186594249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499527-A-T

186594407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499481-A-G

186594705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499259-A-T

http://identifiers.org/hco/4/GRCh38#186594709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45499254-C-A

186594709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499254-C-G

186594709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499254-C-T

186594731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499232-T-A

186594918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45499040-T-C

186594991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498959-T-C

186595027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498933-T-C

186595038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498922-T-C

186595200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498759-G-A

186595256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498706-A-T

186595340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498646-C-T

186595423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498554-G-A

186595547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498374-T-C

186595547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498374-T-G

186595567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498354-T-C

186595568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498353-G-A

186595568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498353-G-T

http://identifiers.org/hco/4/GRCh38#186595572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45498349-C-A

186595609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498295-A-T

186595672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498218-G-A

186595672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45498218-G-C

186595793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45498099-T-C

http://identifiers.org/hco/4/GRCh38#186596325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45497775-C-A

186596325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45497775-C-T

186596397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45497706-A-G

186596516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45497616-G-C

186596516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45497616-G-T

186596520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45497612-G-C

186596529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45497603-G-A

186596529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45497603-G-C

186596602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45497527-G-A

186596602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45497527-G-C

186596608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45497521-G-C

186596608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45497521-G-T

186596788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45497341-A-G

186596848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45497281-G-A

186596863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45497266-G-A

186597205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45496933-T-C

http://identifiers.org/hco/4/GRCh38#186597220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45496918-C-A

186597220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45496918-C-T

http://identifiers.org/hco/4/GRCh38#186597284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45496849-C-A

186597284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45496849-C-G

186597284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45496849-C-T

186597347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45496786-G-A

186597347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45496786-G-T

http://identifiers.org/hco/4/GRCh38#186597357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45496780-A-C

186597358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45496779-T-A

186597407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45496732-G-A

186597407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45496732-G-T

186597421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45496718-C-G

186597590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45495427-T-C

186597636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45495404-A-G

186598014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45495026-C-G

186598014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45495026-C-T

186598101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45494939-A-G

186598142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45494898-G-A

186598142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45494898-G-T

186598168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45494874-A-G

186598168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45494874-A-T

186598188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45494857-T-C

186598193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45494852-T-C

186598195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45494850-G-T

http://identifiers.org/hco/4/GRCh38#186598204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45494841-C-A

186598204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45494841-C-T

http://identifiers.org/hco/4/GRCh38#186598235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45494797-A-C

186598235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45494797-A-G

186599833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45494096-G-T

186599847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45494085-T-A

186599854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45494078-A-G

186599906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45494023-G-A

186599963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45493966-G-A

186599996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45493933-G-A

186599996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: stop gained
orthologous variants: 45493933-G-T

186600011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45493918-G-A

186600014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45493915-T-C

186600023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45493906-G-A

186600203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45493726-G-A

186600233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45493696-G-A

186600233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45493696-G-C

186600275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45493654-C-T

186600278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45493651-T-C

186600401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45493529-A-G

186600458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45493468-T-C

186600509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45493421-A-G

186600509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45493421-A-T

http://identifiers.org/hco/4/GRCh38#186600585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45493344-A-C

186600607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45493319-C-T

186601152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45493107-G-A

186601152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45493107-G-T

186601232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45493032-G-T

http://identifiers.org/hco/4/GRCh38#186601238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45493024-C-A

186601238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45493024-C-T

http://identifiers.org/hco/4/GRCh38#186601240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45493022-C-A

186601240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45493022-C-G

186601240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45493022-C-T

186601297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45492964-G-A

186601490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492762-A-G

http://identifiers.org/hco/4/GRCh38#186601504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45492748-C-A

186601504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492748-C-G

186601522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492732-T-C

186601531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492723-A-G

186601555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492699-T-C

186601555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492699-T-G

http://identifiers.org/hco/4/GRCh38#186601590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45492657-C-A

186601590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492657-C-T

186601610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492633-G-A

186601610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492633-G-T

186601622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492621-T-A

186601622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492621-T-G

186601635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492611-T-A

186601635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492611-T-C

186601661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492587-G-A

186601661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492587-G-T

186601662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492586-T-C

186601666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492582-G-A

186601666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45492582-G-T

http://identifiers.org/hco/4/GRCh38#186601783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45492455-C-A

186601783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45492455-C-T

186602244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45492058-G-C

186602253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45492049-A-T

186602327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45491967-A-T

186602793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45491521-A-T

http://identifiers.org/hco/4/GRCh38#186602810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45491505-C-A

186602810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45491505-C-T

186602945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45491384-G-A

186602971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45491358-C-T

http://identifiers.org/hco/4/GRCh38#186602980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45491349-C-A

186603007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45491322-C-T

http://identifiers.org/hco/4/GRCh38#186603307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45490381-C-A

186603466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45490222-T-A

186603494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45490194-T-C

http://identifiers.org/hco/4/GRCh38#186603594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45490094-C-A

186603594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45490094-C-G

186603594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45490094-C-T

186603640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45490048-A-G

186603741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45489947-T-C

186603788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45489900-A-G

186603865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45489823-G-A

186603865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45489823-G-T

186603923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45489765-C-T

http://identifiers.org/hco/4/GRCh38#186604065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45489630-A-C

186604232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45489488-A-T

186604291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45489433-A-T

186604325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45489402-G-A

186604325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45489402-G-T

http://identifiers.org/hco/4/GRCh38#186604336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45489391-C-A

186604418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45489310-T-C

186604501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45489227-G-A

186604501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45489227-G-C

186604501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45489227-G-T

186604525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45489203-T-C

http://identifiers.org/hco/4/GRCh38#186604552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45489176-C-A

186604552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45489176-C-T

186604638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45489115-A-G

186604711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45489044-G-A

186604711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45489044-G-C

186604743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45489028-G-A

186605799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488901-C-T

186605850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488846-C-G

186605911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488785-T-G

186605918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488778-T-C

186605924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488771-T-A

186605924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488771-T-C

186605933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488766-A-G

186605974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488742-A-T

186605979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488738-G-A

http://identifiers.org/hco/4/GRCh38#186606014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45488694-C-A

186606014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488694-C-T

186606063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45488652-A-G

186606158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45488555-A-T

186606235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488476-T-A

186606235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488476-T-G

186606283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488447-T-A

186606283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488447-T-G

186606296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488434-G-A

186606296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488434-G-T

186606479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488268-C-T

186606572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488172-G-C

186606642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488107-C-T

186606647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488102-C-T

186606672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488077-G-A

186606707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488042-T-A

186606707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488042-T-C

186606710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45488039-G-T

http://identifiers.org/hco/4/GRCh38#186606872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45487887-A-C

186606872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45487887-A-G

186606904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45487855-C-T

186607072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45487745-C-T

http://identifiers.org/hco/4/GRCh38#186607098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45487726-C-A

186609110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45487062-A-G

186609111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45487061-C-T

186609705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45486673-A-G

http://identifiers.org/hco/4/GRCh38#186609756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45486621-C-A

186609756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45486621-C-T

186609829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45486560-T-C

186609995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 45486394-T-C

186610041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45486347-A-G

186610046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45486342-T-C

186610076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45486318-A-T

http://identifiers.org/hco/4/GRCh38#186611235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45484815-C-A

186611235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45484815-C-T

186611255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45484797-G-C

186611310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45484744-A-G

186611678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45484397-C-G

186611678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45484397-C-T

186611742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45484333-T-C

186612831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483715-A-G

186612966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483506-A-G

http://identifiers.org/hco/4/GRCh38#186612975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45483504-C-A

186612975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483504-C-T

186612997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483482-A-T

186613002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483477-G-T

186613039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483453-G-A

186613039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483453-G-T

186613082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483412-T-A

186613082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483412-T-C

186613110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 45483379-T-C

186613191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45483298-G-A

186613191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45483298-G-T

186613228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45483261-A-G

186613228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45483261-A-T

http://identifiers.org/hco/4/GRCh38#186613240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45483249-A-C

186613240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45483249-A-G

186613270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45483219-T-C

186613270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45483219-T-G

186613390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483105-G-A

186613390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483105-G-C

186613390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483105-G-T

186613393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483102-G-T

186613400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45483095-A-G

186613817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482966-A-T

186613826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482957-T-C

186613890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482919-A-T

186614056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482771-T-C

186614056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482771-T-G

186614115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482711-T-C

186614182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482653-C-T

186614237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45482598-C-T

186614312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45482523-G-A

http://identifiers.org/hco/4/GRCh38#186614365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45482471-A-C

186614365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482471-A-G

186614388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482446-G-A

186614388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482446-G-T

186614389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482445-G-A

186614389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482445-G-T

186614396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482437-A-T

http://identifiers.org/hco/4/GRCh38#186614400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45482433-A-C

186614400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482433-A-G

186614400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482433-A-T

186614406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482427-G-A

186614406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482427-G-T

http://identifiers.org/hco/4/GRCh38#186614438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45482395-C-A

186614438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482395-C-T

186614440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482393-A-G

186614440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482393-A-T

186614548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45482290-A-G

http://identifiers.org/hco/4/GRCh38#186614931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45481948-C-A

http://identifiers.org/hco/4/GRCh38#186614946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45481934-C-A

186614962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45481918-A-G

186616579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45481160-C-T

186616651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45481092-G-A

186616697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45481033-C-G

186616923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480791-C-G

186616923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480791-C-T

186616936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480781-G-C

186616936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480781-G-T

http://identifiers.org/hco/4/GRCh38#186616944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45480775-C-A

186616944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480775-C-T

186616946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480773-T-C

186617027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45480693-T-C

186617126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45480594-T-C

186617275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480439-T-C

186617275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480439-T-G

186617286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480428-T-A

186617286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480428-T-G

186617455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480111-T-C

186617548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480039-A-G

186617563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480027-G-T

186617566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480024-G-A

186617566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45480024-G-T

186617696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45479923-A-G

186617700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45479919-T-C

186617827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45479787-G-A

186617920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45479694-G-A

186618307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45479307-A-T

http://identifiers.org/hco/4/GRCh38#186618394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45479220-C-A

186618541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: stop gained
orthologous variants: 45479073-G-C

186618542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45479072-A-T

186618619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45478995-G-A

186618619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45478995-G-C

186618619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45478995-G-T

186618637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45478977-T-C

186618693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45478921-G-A

186618745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: stop gained
orthologous variants: 45478869-G-T

http://identifiers.org/hco/4/GRCh38#186618778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45478836-A-C

186618778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45478836-A-G

186618904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45478710-T-G

186619045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45478569-A-G

http://identifiers.org/hco/4/GRCh38#186619192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45478422-A-C

186619192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45478422-A-G

186619458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45478156-G-A

186619654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477960-T-C

186619678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477936-A-G

186619686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45477928-C-T

186619771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477843-A-G

186620157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45477457-A-G

186620157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45477457-A-T

186620252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477362-T-C

186620398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477216-G-A

186620404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477210-G-A

186620404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477210-G-C

186620407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477207-G-A

http://identifiers.org/hco/4/GRCh38#186620415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45477199-A-C

186620415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477199-A-T

186620443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477171-T-C

186620488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477126-G-A

186620566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477048-G-A

186620566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477048-G-C

186620599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45477015-T-G

186620858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45476756-C-T

186620878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45476736-G-C

186621062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45476552-T-C

186621118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45476496-T-C

186621163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45476451-A-G

186621187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45476427-T-C

186621187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45476427-T-G

186621247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45476367-A-G

186621463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45476151-T-A

186621573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45476041-T-C

186621652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45475962-G-A

186621655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45475959-C-T

186621688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45475926-T-C

186621690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45475924-C-T

186622029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45475589-G-A

186622271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45475347-T-C

186622304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45475314-T-C

186622389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45475228-G-A

186622389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45475228-G-C

186622492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45475136-T-C

186622624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45474983-G-C

186623051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45474606-T-C

http://identifiers.org/hco/4/GRCh38#186623134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45474519-C-A

http://identifiers.org/hco/4/GRCh38#186623211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45474442-A-C

http://identifiers.org/hco/4/GRCh38#186623213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45474440-C-A

http://identifiers.org/hco/4/GRCh38#186623327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45474343-C-A

186623327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45474343-C-T

http://identifiers.org/hco/4/GRCh38#186623446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45474227-C-A

186623520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45474150-A-G

http://identifiers.org/hco/4/GRCh38#186623522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45474148-C-A

186623542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45474127-A-G

186623991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45473439-G-A

186624091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45473347-C-G

http://identifiers.org/hco/4/GRCh38#186624438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45473024-A-C

186624515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45472955-C-T

http://identifiers.org/hco/4/GRCh38#186624751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45472743-C-A

186624808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45472688-G-A

186624901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45472608-T-C

186625206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45472309-G-C

186625229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45472286-G-C

186625277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45472237-A-G

186625381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45472124-T-C

186625391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45472114-G-A

186625587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45471915-C-T

186625665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45471844-T-C

186627494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45471715-C-T

186627558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45471655-C-T

186627629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45471583-G-A

186627909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45471344-T-C

186627934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45471319-T-C

186628027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45471204-G-C

http://identifiers.org/hco/4/GRCh38#186628041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45471191-C-A

186628096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45471132-T-C

186628096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45471132-T-G

186628102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45471126-C-T

http://identifiers.org/hco/4/GRCh38#186628126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45471106-A-C

186628137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45471097-G-A

186628147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 45471087-A-G

186628156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: splice_region_variant, stop_gained
orthologous variants: 45471078-G-C

186628285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45470949-G-A

186628285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45470949-G-C

186628285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45470949-G-T

186628288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45470946-G-A

http://identifiers.org/hco/4/GRCh38#186628318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45470916-A-C

186628333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45470901-T-C

186628360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45470874-C-T

http://identifiers.org/hco/4/GRCh38#186628433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45470764-A-C

186628636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45470527-T-C

186628708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45470455-T-C

186628717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45470446-G-C

186628775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45470388-G-A

186628775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45470388-G-T

186628841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45470334-G-A

186628841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45470334-G-C

186628841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45470334-G-T

186628912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45470249-T-A

186629113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45470078-C-T

http://identifiers.org/hco/4/GRCh38#186629215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45469998-C-A

186629215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45469998-C-T

186629366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45469776-T-C

186629418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45469724-T-C

186629505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45469643-T-C

186629552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45469594-A-G

http://identifiers.org/hco/4/GRCh38#186629859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45469288-C-A

186630023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45469122-A-G

186630053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45469071-G-T

http://identifiers.org/hco/4/GRCh38#186630146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45468973-C-A

186630146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468973-C-G

186630146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468973-C-T

186630334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468814-A-G

186630577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468587-C-T

186630593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468574-G-A

186630618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468550-G-A

186630618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468550-G-T

186630666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468506-C-T

186630738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468434-C-G

186630766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468408-T-C

http://identifiers.org/hco/4/GRCh38#186630829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45468355-C-A

186630829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468355-C-T

186631022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468110-C-T

186631052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45468082-C-T

186631150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45467992-G-A

186631164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45467978-T-A

186632148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45467634-A-T

186632210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45467582-T-C

http://identifiers.org/hco/4/GRCh38#186632221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45467571-A-C

186632224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45467568-A-T

http://identifiers.org/hco/4/GRCh38#186632254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45467534-A-C

186633071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45466713-T-C

186633133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45466661-T-C

186633263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45466533-A-G

186633465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45466329-T-C

http://identifiers.org/hco/4/GRCh38#186633614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45466207-C-A

186633706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45466116-C-T

186633769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45466053-A-G

http://identifiers.org/hco/4/GRCh38#186633905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45465913-C-A

186633946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45465869-G-T

186633965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45465857-A-G

186634016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45465806-T-C

http://identifiers.org/hco/4/GRCh38#186634360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45465534-A-C

http://identifiers.org/hco/4/GRCh38#186634388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45465506-A-C

186634448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45465426-T-C

186634497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45465378-C-G

186634667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45465179-A-G

186634886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45464979-C-G

186634886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45464979-C-T

186634894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45464971-C-T

186635874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45463786-A-T

186635882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45463775-T-C

186635884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45463773-T-C

186635884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45463773-T-G

186635893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45463764-A-T

186635997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45463678-G-T

186636135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45463536-A-G

186636147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45463524-T-C

186636255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45463417-G-A

http://identifiers.org/hco/4/GRCh38#186636300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45463374-A-C

186636404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45463256-T-C

186636437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45463225-A-T

http://identifiers.org/hco/4/GRCh38#186636483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45463200-C-A

http://identifiers.org/hco/4/GRCh38#186636496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45463187-A-C

186636496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45463187-A-T

186636576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45463169-T-C

186636595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45463150-T-C

186636613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45463132-G-A

186636727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45463018-G-A

186636918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 45462825-T-G

186637227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45462750-T-A

186637356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45462683-T-C

186637696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45462376-A-G

186637824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45462229-C-G

186637870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45462184-T-A

http://identifiers.org/hco/4/GRCh38#186637949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45462083-C-A

186637949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45462083-C-T

186638137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45461904-C-T

186638237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45461813-T-C

186638254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45461795-T-C

186638567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45461477-C-T

http://identifiers.org/hco/4/GRCh38#186638923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45461158-C-A

186638923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45461158-C-T

186638988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45461117-A-G

186639173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460978-G-A

186639241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460903-C-T

186639320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460824-A-T

186639359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460797-T-C

186639460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460698-G-A

http://identifiers.org/hco/4/GRCh38#186639594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45460624-C-A

186639594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460624-C-T

186639600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460605-A-G

186639635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460572-A-G

186639635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460572-A-T

186639636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460571-T-A

186639636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460571-T-C

186639651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460556-A-G

186640233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460225-G-C

186640256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460202-C-T

186640431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45460032-C-G

186640496-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45459963-T-A

http://identifiers.org/hco/4/GRCh38#186640506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45459952-C-A

186640572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45459898-C-T

186640573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45459897-T-G

186640643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45459787-T-G

186640781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45459646-T-C

186643457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45457826-A-T

http://identifiers.org/hco/4/GRCh38#186643574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45457704-A-C

186643583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45457695-T-G

186643618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45457671-G-A

186643717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45457562-A-T

186643758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45457534-C-T

http://identifiers.org/hco/4/GRCh38#186643790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45457495-C-A

186643790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45457495-C-T

186643888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45457401-G-A

186643888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45457401-G-C

186644154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45457166-T-A

186644154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45457166-T-C

186644246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45457074-G-A

186644246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45457074-G-C

186644286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45457034-C-T

186644524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45456803-T-C

186646006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45456378-T-A

186646006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45456378-T-C

186646205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45456189-A-G

186646409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45455998-G-A

186646444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45455965-G-T

186646465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45455944-C-T

186646479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45455930-G-T

186646752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45455675-C-T

186646762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45455665-G-A

186647975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45454266-G-A

186648227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45454064-C-T

186651246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45452512-T-G

186651374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45452398-T-C

186651392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45452381-G-C

http://identifiers.org/hco/4/GRCh38#186651394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45452379-C-A

186651394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45452379-C-T

186651396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45452377-C-G

186651647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45452106-C-T

186651711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45452039-G-A

http://identifiers.org/hco/4/GRCh38#186651814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45451929-C-A

186651814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45451929-C-G

186651814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45451929-C-T

186651972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45451772-T-C

186652019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45451725-T-A

http://identifiers.org/hco/4/GRCh38#186652424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45451319-A-C

186652505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45451253-A-G

186652665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45451120-A-G

186652902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45450858-G-A

186653245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45450505-C-G

186654028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45449837-T-C

186654189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45449696-T-C

186654240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45449645-C-G

186654406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45449489-T-A

186655183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45449071-A-T

186655210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45449055-C-T

186656401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45447985-C-G

186656401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45447985-C-T

186656422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45447973-C-G

186656424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45447971-G-A

186656465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45447928-G-A

186656696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45447724-A-G

186656759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45447659-C-T

186656830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45447581-A-T

186656851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45447560-G-A

http://identifiers.org/hco/4/GRCh38#186656939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45447461-C-A

http://identifiers.org/hco/4/GRCh38#186657083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45447357-C-A

186657083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45447357-C-T

http://identifiers.org/hco/4/GRCh38#186657149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45447289-A-C

186657274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45447182-A-G

186657328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45447127-G-A

186657497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45446967-G-T

186657704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45446800-G-A

http://identifiers.org/hco/4/GRCh38#186657802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45446720-C-A

186657984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45446575-T-A

http://identifiers.org/hco/4/GRCh38#186658304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45446256-A-C

186658305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45446255-G-A

http://identifiers.org/hco/4/GRCh38#186658539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45446048-C-A

186660029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45445440-C-T

186660033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45445436-C-G

186660034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45445435-C-T

186660215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45445258-G-A

186660314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45445148-C-T

http://identifiers.org/hco/4/GRCh38#186660334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45445134-A-C

186660334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45445134-A-G

186660424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45445047-T-C

http://identifiers.org/hco/4/GRCh38#186663166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45442411-A-C

186663166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45442411-A-T

186663258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45442321-G-T

186663262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45442317-A-G

186663268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45442311-A-G

186663328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45442251-T-C

186663454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45442125-G-A

186663454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45442125-G-T

186663472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45442107-G-A

186663583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45441996-C-T

186663630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45441956-A-G

186663631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45441955-A-G

http://identifiers.org/hco/4/GRCh38#186663668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45441914-C-A

186663683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45441899-A-G

186663688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45441894-T-C

186663788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45441844-G-A

186663922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45441639-T-C

http://identifiers.org/hco/4/GRCh38#186663996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45441488-A-C

186664056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45441431-C-T

186664136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45441378-T-C

186664240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45441256-A-G

186664323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45441179-C-T

http://identifiers.org/hco/4/GRCh38#186664505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45441013-C-A

186664542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45440977-T-C

186664582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45440961-T-C

186666612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45440737-A-G

186668547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45439926-C-T

186668571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45439902-G-A

186668823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45439784-C-T

186668853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45439751-T-C

186669255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45439256-C-T

186669308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45439200-G-T

186669383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45439139-G-A

186669383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45439139-G-C

186669405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45439117-A-G

186669428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45439095-G-T

186669797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45438166-C-T

186670096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45437873-T-G

186670124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45437841-G-C

186670125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45437840-T-G

186670129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45437836-G-T

186672470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45436750-T-G

186673189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45436288-G-A

186673483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45435722-A-T

186673780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45435424-A-G

186673880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45435348-T-G

http://identifiers.org/hco/4/GRCh38#186674198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45434917-A-C

186674239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45434878-T-G

http://identifiers.org/hco/4/GRCh38#186674277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45434844-A-C

186674422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45434689-A-G

186674503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45434596-T-C

186674579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45434526-A-G

186674757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45434237-G-C

186674807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45434188-G-A

http://identifiers.org/hco/4/GRCh38#186674819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45434171-A-C

186674868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45434103-T-C

186674889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45434082-C-G

186675842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45433968-T-A

186675915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45433890-T-C

186675972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45433833-G-C

186676511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45433477-A-T

186676609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45433378-T-C

186676750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45433243-G-C

186676793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45433194-G-A

186676894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45433088-T-C

186677019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45432969-C-T

186677076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45432931-T-G

186677280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45432753-T-C

186677312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45432713-G-C

186677328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45432697-T-C

186677330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45432695-T-A

186677492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45432548-T-C

186677492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45432548-T-G

186677528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45432516-G-A

http://identifiers.org/hco/4/GRCh38#186677861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45432231-A-C

186682604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45430433-A-G

186682640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45430391-T-C

186682893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45430145-C-G

186683085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45429960-C-G

http://identifiers.org/hco/4/GRCh38#186683390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45429667-C-A

186683390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45429667-C-T

http://identifiers.org/hco/4/GRCh38#186683472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45429575-A-C

186683528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45429517-C-G

186683621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45429311-T-G

186683644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45429283-T-A

186683708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45429232-G-C

186683735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45429205-C-T

186683895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45429067-A-T

186684172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45428807-T-A

http://identifiers.org/hco/4/GRCh38#186684457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45428544-A-C

186684671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45428329-A-G

186685280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45427775-T-A

186685522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45427482-T-C

186685774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45427233-T-C

186685889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45427104-T-C

186685906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45427087-A-T

186686097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45426880-A-G

186686184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45426792-C-T

186686302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45426683-C-T

186686394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45426616-A-G

186686417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45426593-G-C

186686485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45426519-T-A

186686831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45425882-T-C

186687287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45425412-C-G

186687293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45425406-G-C

186687785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45425121-A-G

186687829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45425077-A-G

186688078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45424854-G-A

186688078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45424854-G-T

186688219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45424719-T-A

http://identifiers.org/hco/4/GRCh38#186688247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45424691-C-A

186688247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45424691-C-T

186688385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45424564-C-T

http://identifiers.org/hco/4/GRCh38#186688400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45424547-C-A

186688658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45424303-C-T

http://identifiers.org/hco/4/GRCh38#186688670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45424291-C-A

186689249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45423690-T-C

186689349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45423613-A-G

186689545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45423458-C-T

186689695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45423328-C-G

186689705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45423318-G-C

186689799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45423245-G-A

186689808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45423237-C-T

http://identifiers.org/hco/4/GRCh38#186690060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45422998-C-A

186692158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45421860-A-G

186692166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45421858-A-G

186692262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45421777-T-C

186692319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45421678-A-T

http://identifiers.org/hco/4/GRCh38#186692537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45421434-C-A

186692537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45421434-C-T

186693216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45421148-C-T

186694442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45420314-C-T

186694457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45420299-G-A

186694534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45420206-T-C

http://identifiers.org/hco/4/GRCh38#186695057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45419605-A-C

186695133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45419529-G-A

186695178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45419478-A-G

186695359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45419299-C-G

186695359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45419299-C-T

186695366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45419292-T-C

186695614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45419037-G-A

186696218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45417851-T-A

http://identifiers.org/hco/4/GRCh38#186696232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45417837-A-C

186696232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45417837-A-G

186696420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45417566-G-A

186696420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45417566-G-C

186696450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45417536-T-C

186697116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45416724-C-T

186698047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45416187-G-A

186698252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45416006-A-G

186698344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45415925-G-A

186698545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45415760-C-T

186698661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45415611-C-T

186698880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45415380-A-G

186698940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45415325-T-C

186699014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45415249-C-T

186699020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45415243-T-C

186699116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45415138-G-A

186699139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45415115-C-T

186699155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45415090-A-G

186699184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45415049-T-C

186699504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45414758-T-C

186699670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45414598-T-A

186699720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45414553-G-A

186700244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45414026-G-C

186700295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413970-G-A

186700307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413958-C-G

186700307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413958-C-T

186700649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413479-G-C

186700660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413469-A-T

http://identifiers.org/hco/4/GRCh38#186700776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45413356-C-A

186700776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413356-C-T

186700777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413355-G-A

186700777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413355-G-C

186700821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413311-G-A

186700843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413289-T-A

186700970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413108-A-T

186701071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413017-C-T

186701102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413000-G-A

186701102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45413000-G-T

http://identifiers.org/hco/4/GRCh38#186701104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45412998-A-C

186701105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45412997-T-A

http://identifiers.org/hco/4/GRCh38#186701141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45412960-A-C

186701206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45412898-T-G

186701212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45412892-T-G

186701381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45412757-G-C

186701426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45412716-T-C

186701614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45412514-C-T

186701793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 45412356-T-A

186701862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45412305-G-A

186701903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45412265-C-G

186701903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45412265-C-T

186701918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45412249-C-T

186702335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45411744-A-G

186702417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45411663-C-T

186702422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45411662-C-G

186702648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45411474-G-A

186702694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45411431-C-T

186702734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45411408-C-T

186702831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 45411331-G-C

186703188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45410657-C-T

186703562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45410332-A-G

186703563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45410331-G-A

186703563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45410331-G-C

186703726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: -C-T

186703883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: -G-A

186703989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45409165-G-A

186704012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45409145-T-C

186704016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 45409141-T-C

http://identifiers.org/hco/4/GRCh38#186704096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45409068-A-C

http://identifiers.org/hco/4/GRCh38#186704111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45409052-C-A

186704213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45408945-A-G

186704583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45408580-T-C

186704860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45408336-T-C

186705270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45408234-T-C

186705447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45408066-T-C

186705700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45407838-T-C

186706234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45406743-A-G

186706442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45406619-A-G

http://identifiers.org/hco/4/GRCh38#186706454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45406607-A-C

http://identifiers.org/hco/4/GRCh38#186706456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45406605-C-A

186706456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45406605-C-T

186706552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45406526-A-T

http://identifiers.org/hco/4/GRCh38#186706554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45406525-C-A

186706661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45406418-A-G

186706664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45406415-G-A

186706664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45406415-G-T

186706679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45406400-C-G

186706679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45406400-C-T

186706702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45406377-T-C

186706702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45406377-T-G

186706715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45406364-A-G

186706736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45406343-G-A

186706825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45406254-C-T

186706834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45406245-A-G

186706834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45406245-A-T

186706949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45406130-C-G

186706961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: stop gained
orthologous variants: 45406118-A-T

186707109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45405970-G-A

186707109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405970-G-T

186707161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45405918-A-G

186707294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405785-T-G

186707330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405749-T-A

186707393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405686-A-T

186707408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405671-A-T

186707461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45405618-G-T

186707528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405551-A-G

186707546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405533-T-C

186707673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405406-T-C

186707673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405406-T-G

186707693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405386-T-A

186707756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405323-T-C

186707779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45405300-C-G

186707779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45405300-C-T

186707885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405194-G-A

186707885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405194-G-C

186707920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45405159-T-C

186708035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405044-T-C

http://identifiers.org/hco/4/GRCh38#186708056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45405023-A-C

186708056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45405023-A-G

186708164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45404915-G-C

186708212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45404867-C-T

186708275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45404804-G-A

186708287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45404792-T-C

186708366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45404713-C-T

http://identifiers.org/hco/4/GRCh38#186708392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45404687-C-A

186708399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45404680-G-A

186708488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45404591-G-C

186708661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45404418-T-C

186708769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45404310-A-G

186708830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45404249-T-C

186708836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45404243-C-T

186708860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45404219-A-G

186708868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45404211-G-A

186708914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45404165-G-C

186709007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45404072-G-A

186709066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45404013-A-G

186709142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45403937-A-G

186709212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: synonymous variant
orthologous variants: 45403867-A-G

186709246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45403833-C-T

186709280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45403799-T-A

186709439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45403640-T-C

186709475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: stop gained
orthologous variants: 45403604-A-T

186709584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45403495-G-C

186709584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45403495-G-T

http://identifiers.org/hco/4/GRCh38#186709604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45403475-A-C

186709640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45403439-A-G

186709643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45403436-T-C

186709737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45403339-G-A

186709737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: missense variant
orthologous variants: 45403339-G-C

186709857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45403212-G-T

http://identifiers.org/hco/4/GRCh38#186709962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45403117-A-C

186709962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45403117-A-T

186710003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45403100-T-G

186710338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45402620-T-C

186710351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45402607-C-T

186710586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45402363-T-C

186711416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45401543-A-T

186712041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45401167-T-C

186712102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45401108-A-T

186712155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45401045-A-T

186712162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45401038-G-A

186712232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45400970-A-G

186712373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45400848-G-C

186712577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45400617-C-T

http://identifiers.org/hco/4/GRCh38#186712629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45400575-C-A

186715412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45398325-T-A

186715412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45398325-T-C

186715426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45398311-C-T

186715477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45398248-C-T

186715512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45398210-C-T

186715543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45398181-G-C

186715678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45398043-C-G

186715678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45398043-C-T

186715695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45398026-A-G

186715725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45397996-A-T

http://identifiers.org/hco/4/GRCh38#186715835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45397898-A-C

186715881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45397849-A-G

186715889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45397841-T-C

186715925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45397806-C-T

186715969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45397768-G-A

186716009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45397729-G-T

186716012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45397726-G-A

http://identifiers.org/hco/4/GRCh38#186716021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45397717-A-C

186716021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45397717-A-G

186716022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45397716-C-T

186716041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45397697-T-C

186717605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45397138-A-G

186717606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45397137-G-A

186717855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45396903-C-G

186717969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45396801-A-G

http://identifiers.org/hco/4/GRCh38#186717985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45396784-A-C

186718122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45396649-A-G

http://identifiers.org/hco/4/GRCh38#186718696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45396457-A-C

186718767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45396392-C-T

186718768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45396391-G-A

186718768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45396391-G-T

186718843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45396294-T-A

186718948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45396113-G-A

186718948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45396113-G-C

186718960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45396101-T-C

186718960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45396101-T-G

186719106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45395991-C-G

186719133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45395974-C-G

http://identifiers.org/hco/4/GRCh38#186719155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45395949-C-A

186719155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45395949-C-T

186719196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45395908-G-A

http://identifiers.org/hco/4/GRCh38#186719206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45395898-A-C

186719268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45395856-C-G

http://identifiers.org/hco/4/GRCh38#186720051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45394910-C-A

186720051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45394910-C-G

186720146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45394819-A-G

186720455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45394515-C-T

186720624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45394363-G-A

186720977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45394035-T-C

http://identifiers.org/hco/4/GRCh38#186721093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45393920-A-C

186721136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45393879-T-C

186721247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45393774-G-A

186721302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45393528-T-G

186722262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45392712-T-C

186722311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45392650-G-C

http://identifiers.org/hco/4/GRCh38#186723066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45391921-A-C

186723220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45391791-T-A

186723599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45391414-G-C

186723620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45391406-A-T

http://identifiers.org/hco/4/GRCh38#186723726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#45391299-C-A

186723726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45391299-C-G

186723729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45391296-C-G

186723729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45391296-C-T

186723833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 45391212-G-C

http://identifiers.org/hco/4/GRCh38#186723863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45391185-C-A

186723863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45391185-C-G

186723863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45391185-C-T

186723947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45391091-G-A

186723994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45391044-C-T

186724024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45391019-G-A

186724143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45390914-G-T

186724173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45390881-T-A

186724188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45390859-A-G

186724225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45390801-A-G

186724435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45390578-T-C

186724459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45390546-G-A

http://identifiers.org/hco/4/GRCh38#186724475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#45390507-C-A

186724475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45390507-C-T

186724501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45390480-T-C

186724796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45390195-G-A

186725183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45389812-C-T

186725281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45389713-C-T

186725417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45389553-G-A

186725678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45389331-C-T

186725877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45389143-C-T

186725937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45389076-T-C

186725942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45389069-G-C

186726194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron variant
orthologous variants: 45388813-G-T

186726255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45388752-G-A

186726255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45388752-G-T

186726273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: intron_variant, undefined
orthologous variants: 45388735-A-G

186726369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 5 prime UTR variant
orthologous variants: 45388641-C-T

186726513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 5 prime UTR variant
orthologous variants: 45388493-C-G

186726513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3595
most severe consequence: 5 prime UTR variant
orthologous variants: 45388493-C-T