56719060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873814-A-G

56719070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873804-T-C

56719323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873629-C-G

56719345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873608-A-G

56719507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873459-T-G

56719509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873457-A-T

56719556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873435-A-G

56719562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873434-T-C

56719562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873434-T-G

56719607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873392-G-A

56719607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873392-G-T

56719625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873375-G-A

56719625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873375-G-T

56719658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873360-G-T

56719664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873354-G-A

56719664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 104873354-G-T

56719711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104873306-A-G

56719897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104873184-A-G

56719897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104873184-A-T

56719944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104873161-G-A

56719967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104873141-T-C

56720002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104873100-T-C

http://identifiers.org/hco/1/GRCh38#56720006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104873096-A-C

56720006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104873096-A-G

56720150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104872974-G-T

56720187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104872947-T-A

56720187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104872947-T-C

56720316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104872818-A-G

http://identifiers.org/hco/1/GRCh38#56720477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104872682-A-C

http://identifiers.org/hco/1/GRCh38#56720578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104872590-C-A

56720751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104872587-T-A

56720831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104872568-C-T

http://identifiers.org/hco/1/GRCh38#56721245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104872264-A-C

56721278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104872233-A-G

56721847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104871882-T-A

56722001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104871754-A-G

56722228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104871596-C-G

56722228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104871596-C-T

56722370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104871461-G-A

56722370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104871461-G-T

56722439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104871421-G-C

56722571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104871296-A-G

56722720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104871160-G-A

56722774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104871111-A-G

56722884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104871042-C-T

56722950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870983-T-C

56723429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870716-G-A

56723505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870666-A-T

56723507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870664-A-G

56723534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870639-T-G

http://identifiers.org/hco/1/GRCh38#56723552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104870623-A-C

56723552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870623-A-G

56723552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870623-A-T

56723582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870582-A-G

http://identifiers.org/hco/1/GRCh38#56723587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104870577-C-A

56723587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 104870577-C-G

56723640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104870524-A-G

56723654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 104870510-G-A

56723654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 104870510-G-C

56723654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 104870510-G-T

http://identifiers.org/hco/1/GRCh38#56723750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104870414-A-C

56723776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870388-G-A

56723776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870388-G-T

56723801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870363-T-G

56723805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870359-A-G

56723805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870359-A-T

56723843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104870353-A-G

56726191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104868008-C-G

56726455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104867769-T-G

56726462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104867762-G-C

56726512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104867717-G-C

56726512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104867717-G-T

56726578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104867651-T-G

56726689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104867524-A-G

http://identifiers.org/hco/1/GRCh38#56726812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104867438-A-C

56726974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104867262-T-C

56737017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104861209-T-A

56737019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104861207-A-G

56737051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104861177-T-C

56737078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104861150-A-G

56737152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104861063-G-T

56737154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104861061-T-C

56737184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104861035-A-G

http://identifiers.org/hco/1/GRCh38#56737276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104860952-C-A

56737288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104860945-A-G

56737295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104860938-A-G

http://identifiers.org/hco/1/GRCh38#56737354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104860890-A-C

http://identifiers.org/hco/1/GRCh38#56737489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104860794-A-C

56737577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104860712-T-C

56737598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104860628-T-C

56737767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104860226-A-G

56737822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104860064-T-G

56737890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104859986-G-C

56738022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104859875-C-T

56738045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104859855-A-G

http://identifiers.org/hco/1/GRCh38#56738233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104859695-A-C

56738455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104859509-A-G

http://identifiers.org/hco/1/GRCh38#56738478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104859488-C-A

56738478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104859488-C-G

56738499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104859467-T-G

http://identifiers.org/hco/1/GRCh38#56738522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104859444-C-A

http://identifiers.org/hco/1/GRCh38#56738563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104859418-C-A

56738563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104859418-C-T

56738575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104859406-A-G

56738686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104859288-G-A

http://identifiers.org/hco/1/GRCh38#56738726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104859254-C-A

56738748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104859212-G-T

56738770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104859183-T-C

56738920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104858966-G-A

56739592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104858329-A-G

56740488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104857888-T-C

56740629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104857791-G-T

56740739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104857672-T-C

http://identifiers.org/hco/1/GRCh38#56741483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104857175-C-A

56741486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104857172-T-C

56741511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104857150-T-C

56741620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104857059-C-T

56741699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856985-C-T

56742025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856685-T-C

56742091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856650-C-T

http://identifiers.org/hco/1/GRCh38#56742131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104856609-C-A

56742131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856609-C-T

56742152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856593-G-T

56742168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104856577-T-G

56742211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 104856531-T-C

56742236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856506-A-G

56742316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856472-G-T

56742583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856219-G-A

56742653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856174-C-T

56742657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856170-T-A

56742657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856170-T-C

56742727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856100-T-A

56742768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104856061-A-G

56743748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104853364-T-C

56743782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104853330-A-G

http://identifiers.org/hco/1/GRCh38#56743799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104853301-C-A

56743883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104853248-A-G

56743929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104853211-A-T

56743963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104853178-A-G

56744025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 104853137-C-G

56744044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104853118-A-T

56744049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104853113-G-T

56744089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104853074-C-T

56744096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104853062-T-A

http://identifiers.org/hco/1/GRCh38#56744282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104852876-A-C

56744319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852842-G-T

56744363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852799-G-A

56744367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852795-G-T

56744406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852403-A-G

56744508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852313-T-A

http://identifiers.org/hco/1/GRCh38#56744511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104852310-A-C

56744513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852308-T-C

56744515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852306-C-T

56744570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852254-G-A

56744593-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852236-C-G

56744651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852185-T-A

56744651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852185-T-C

56744700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852080-C-T

56744758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852030-A-G

56744782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104852005-A-G

56744836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104851943-G-T

http://identifiers.org/hco/1/GRCh38#56744843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104851934-C-A

56744873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104851906-C-T

56750471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104848069-C-T

56750662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847906-G-A

56750948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847645-T-A

56750948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847645-T-G

56750950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847643-A-G

56750958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847635-T-C

56750958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847635-T-G

56751031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847565-A-T

56751043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 104847553-C-T

56751236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847359-G-A

56751236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847359-G-T

http://identifiers.org/hco/1/GRCh38#56751286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104847309-A-C

http://identifiers.org/hco/1/GRCh38#56751345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104847255-C-A

56751345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847255-C-T

56751348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847252-T-A

56751348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847252-T-G

56751349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847251-A-G

56751560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104847065-C-G

http://identifiers.org/hco/1/GRCh38#56751827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104846794-C-A

56751874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104846728-A-T

56751888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104846714-T-C

56752124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104846471-G-A

56752137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104846450-G-A

56752240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104846353-T-C

56752263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104846330-C-T

56753824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104846276-G-A

56753824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104846276-G-T

56753875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104846225-G-T

56753880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 104846220-T-A

56753886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 104846214-T-A

56753886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104846214-T-G

http://identifiers.org/hco/1/GRCh38#56753908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104846192-C-A

56753926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 104846168-A-G

56753926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 104846168-A-T

56753950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104846146-G-A

56753950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104846146-G-T

56754100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104846020-T-C

56754110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104846010-T-C

http://identifiers.org/hco/1/GRCh38#56754237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104845903-C-A

56754343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845805-T-A

56754452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845702-C-G

56755731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845560-G-A

56755809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845486-C-T

56755853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845442-C-T

56755862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845433-G-A

56755862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845433-G-T

56755958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845286-A-G

56755958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845286-A-T

56755960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845284-A-G

56755981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845263-T-C

http://identifiers.org/hco/1/GRCh38#56756054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104845196-C-A

56756054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845196-C-T

http://identifiers.org/hco/1/GRCh38#56756070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104845180-A-C

56756071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845179-A-G

56756154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845110-G-T

56756222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104845057-A-G

56756422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104844859-G-A

56756599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104844687-A-G

56756689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104844615-A-G

http://identifiers.org/hco/1/GRCh38#56756690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104844614-C-A

56756691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104844613-A-T

56756714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104844590-C-T

56756744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104844560-G-A

56756852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104844487-C-T

56756921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104844406-T-C

56756938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104844389-A-G

56757051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104844289-A-T

56758204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104843973-T-C

56758205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104843972-G-A

56758511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104843655-C-G

56758565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104843605-G-A

56758565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104843605-G-T

http://identifiers.org/hco/1/GRCh38#56758567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104843603-C-A

56758567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104843603-C-T

http://identifiers.org/hco/1/GRCh38#56758668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104843537-C-A

56758668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104843537-C-G

56758668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104843537-C-T

56758671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104843534-G-A

56758671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104843534-G-T

http://identifiers.org/hco/1/GRCh38#56758681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104843524-C-A

56758701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104843505-A-G

56760495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104842236-A-T

56760534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104842155-A-T

56760701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104842003-T-C

56760882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104841793-T-A

56761039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104841576-G-A

56761041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104841574-A-G

56761071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104841544-G-A

56761347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104841339-G-C

56761846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104840896-T-C

56761846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104840896-T-G

56762087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104840683-G-A

56762110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104840664-A-G

56762343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104840423-G-A

56763180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104839739-G-A

56765985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104838053-A-G

56766036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104838001-T-C

56766977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104837213-C-G

56767014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104837176-C-G

56767014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104837176-C-T

http://identifiers.org/hco/1/GRCh38#56767361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104836847-C-A

56767361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104836847-C-T

http://identifiers.org/hco/1/GRCh38#56767527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104836700-A-C

56767656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104836450-T-A

56767722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104836386-G-C

56767722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104836386-G-T

56767726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104836382-G-A

56767726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104836382-G-T

56767758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104836350-G-C

56767814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104836297-G-T

56767821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 104836289-A-G

56767844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104836266-T-C

56767885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104836225-T-C

56767894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104836216-G-C

56767959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104833042-T-A

56768550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104832563-G-A

56770501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104831465-A-G

56770501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104831465-A-T

56770540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104831412-T-C

56770619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104831334-T-G

56770689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104831270-G-A

56770955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104831007-T-C

56771126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104830824-T-A

56771221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104830765-G-A

56771237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104830750-A-G

http://identifiers.org/hco/1/GRCh38#56771297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104830693-C-A

56771602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104830476-G-C

56771628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104830472-G-C

56771698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104830436-T-C

56771771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104830365-T-C

56771771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104830365-T-G

56771929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104830173-T-G

56771930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104830172-G-A

56772020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104829904-G-A

56772022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104829902-T-C

56772022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104829902-T-G

56772174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104829745-C-T

56772318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104829597-A-G

56772395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104829487-A-T

56772492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104829367-C-T

56772729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104829156-A-G

56772808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104829077-T-C

56773185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104828721-A-G

56773264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104828645-C-T

56773536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104828402-G-A

56773536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104828402-G-C

56773662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104828300-T-C

56773787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104828198-T-G

56773850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104828135-T-C

56774068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104827706-T-C

56774145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104827632-G-A

56774145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104827632-G-C

56774145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104827632-G-T

56774151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104827626-A-G

http://identifiers.org/hco/1/GRCh38#56774194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104827585-A-C

56774305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104827486-T-C

56774346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104827450-C-T

56774350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104827446-G-A

56774393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104827414-C-T

56775313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104825037-A-G

http://identifiers.org/hco/1/GRCh38#56775362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104824986-A-C

56775563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104824772-A-G

56775750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104824586-A-G

56776638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104818501-C-T

56776820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104818325-T-C

56776911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104818245-T-A

http://identifiers.org/hco/1/GRCh38#56776950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104818203-C-A

56776950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104818203-C-T

http://identifiers.org/hco/1/GRCh38#56777485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104817790-C-A

56777679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104817614-A-G

56777701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104817592-T-C

56777722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104817572-T-C

http://identifiers.org/hco/1/GRCh38#56777842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104817454-A-C

56777863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104817433-C-T

56777967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104817065-T-A

56777971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104817061-A-G

56778120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816926-G-A

56778120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816926-G-T

56778148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816899-T-C

56778354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816721-T-C

56778435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816530-T-C

http://identifiers.org/hco/1/GRCh38#56778499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104816434-C-A

56778529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816404-T-A

56778537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816396-G-C

56778559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816374-T-C

56778591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816343-G-A

http://identifiers.org/hco/1/GRCh38#56778716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104816249-A-C

56778756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816209-A-T

56778783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816185-A-G

56778784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816184-T-C

56778846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816131-C-G

56778900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816111-G-A

56778925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104816087-T-C

56779036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815973-G-A

56779228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815830-T-C

56779234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815822-A-G

56779675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815417-G-A

56779675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815417-G-C

56779735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815368-A-G

56779735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815368-A-T

56779798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104815307-C-T

http://identifiers.org/hco/1/GRCh38#56779917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104815215-C-A

http://identifiers.org/hco/1/GRCh38#56780242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104814948-C-A

56780242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814948-C-T

56780259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814930-C-G

56780439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814853-T-A

56780439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814853-T-C

56780476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814830-G-A

http://identifiers.org/hco/1/GRCh38#56780582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104814736-C-A

56780595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814716-G-A

56780714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814619-G-A

http://identifiers.org/hco/1/GRCh38#56780800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104814517-C-A

56780800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814517-C-T

56780802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814515-A-T

56780811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814506-C-G

56780960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814360-G-A

56780980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814340-G-A

56781070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814253-G-A

56781077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814246-T-C

56781090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814233-A-G

56781174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814162-T-C

56781223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814116-T-A

56781332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104814002-A-G

56781350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104813978-C-T

56781657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104813687-A-G

56781675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104813669-T-A

56781675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104813669-T-C

56781939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104813406-G-T

56782591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104812622-T-C

56782594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104812619-G-C

56782610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104812603-C-T

http://identifiers.org/hco/1/GRCh38#56782852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104812329-A-C

56782852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104812329-A-T

56782983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104812195-C-G

56782983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104812195-C-T

56783366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104811821-C-T

56783557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104811626-G-T

56783589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104811594-T-C

56783591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104811592-G-T

http://identifiers.org/hco/1/GRCh38#56783612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104811571-A-C

56783799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104811471-T-C

56784532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810993-A-G

56784532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810993-A-T

56784575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810944-T-C

56784640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810548-C-T

56784742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810359-T-C

56784837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810280-A-G

http://identifiers.org/hco/1/GRCh38#56784885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104810226-A-C

56784892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810219-C-G

56784892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810219-C-T

56784902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810207-C-T

56785104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104810008-C-G

56785686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809506-C-G

56785990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809197-G-A

56786027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809159-T-C

56786042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809144-G-A

56786155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104809054-C-T

56786241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808997-C-T

http://identifiers.org/hco/1/GRCh38#56786290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104808953-A-C

56786644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808621-G-A

56786706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808567-G-A

56786722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808551-A-G

56786845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808430-C-T

56786903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808375-G-T

56787030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808241-C-G

56787030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808241-C-T

56787060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808213-G-A

56787060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808213-G-C

56787060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808213-G-T

56787124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104808146-T-A

56787395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104807931-A-G

http://identifiers.org/hco/1/GRCh38#56787485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104807872-C-A

56787485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104807872-C-G

56787531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104807831-G-A

56787594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104807770-A-T

56788620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806369-C-T

56788693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806306-T-C

56788705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806294-G-A

http://identifiers.org/hco/1/GRCh38#56788737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104806262-C-A

56788772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806227-G-A

56788772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806227-G-T

http://identifiers.org/hco/1/GRCh38#56788832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104806171-C-A

56788832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806171-C-T

http://identifiers.org/hco/1/GRCh38#56788839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104806164-C-A

56788839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806164-C-T

56788841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806162-C-G

56788841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806162-C-T

56788878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806129-T-C

56788902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806112-A-G

56788910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104806104-G-C

56789047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104805953-G-A

56789059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104805941-G-A

56789105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104805895-G-A

56789105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104805895-G-C

56789121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104805879-A-T

56789192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104805822-G-T

56789407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104805631-C-T

56789598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104805578-G-A

56789799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104805372-G-A

56789799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104805372-G-T

56790185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804993-G-T

56790189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804989-T-C

56790235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804948-C-T

56790275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804908-C-T

http://identifiers.org/hco/1/GRCh38#56790276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104804907-C-A

56790343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804837-T-A

56790409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804766-T-C

56790418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804757-T-C

56790527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804643-C-T

56790658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104804537-T-A

http://identifiers.org/hco/1/GRCh38#56791857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104803211-C-A

56791934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104803149-G-A

56791934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104803149-G-T

http://identifiers.org/hco/1/GRCh38#56791941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104803142-C-A

56791941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104803142-C-T

56792192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104802910-A-G

56792192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104802910-A-T

56792297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 104802805-T-C

56792361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104802741-C-G

http://identifiers.org/hco/1/GRCh38#56792530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104802572-C-A

56792576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104802526-T-C

56792629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104802473-G-A

56792629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104802473-G-C

56792629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104802473-G-T

56792688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 104802414-C-T

56792828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104802291-A-G

56792880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104802266-T-A

56793174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104802021-C-T

56793959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104801427-C-G

http://identifiers.org/hco/1/GRCh38#56794055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104801334-C-A

56794055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104801334-C-G

56794085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104801308-C-T

56794178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104801231-T-C

56794252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104801144-C-T

56794519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104800688-T-C

56794952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104800122-A-T

56795005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104800092-T-C

56795034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104800076-C-G

http://identifiers.org/hco/1/GRCh38#56795063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104800065-A-C

56795082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104800046-T-C

56795427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104799680-G-T

56795610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104799497-T-C

56795917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104799198-T-C

56795958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104799156-A-G

56796013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104799084-G-T

56796361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798758-C-T

56796617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798514-G-A

56796617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798514-G-T

56796652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798479-A-G

http://identifiers.org/hco/1/GRCh38#56796669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104798462-C-A

56796669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798462-C-T

56796706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798429-C-G

56798052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798309-T-C

56798078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798294-G-T

56798138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798234-G-A

56798158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104798214-C-T

56798251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104798127-T-A

56798636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104797777-T-C

56800239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104797458-G-C

56802260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104796999-A-G

56802305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104796953-G-A

56802340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104796910-C-T

56802923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104795753-C-T

56803440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104795336-A-G

http://identifiers.org/hco/1/GRCh38#56803563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104795209-A-C

56803571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104795200-G-T

56803725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104794541-G-A

56803735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104794528-A-G

56803879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104794386-C-T

56804000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104794267-A-G

56804002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104794265-T-A

56804002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104794265-T-C

56804156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104794136-T-C

56804248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104794044-T-C

56804820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104793817-G-T

http://identifiers.org/hco/1/GRCh38#56804857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104793781-C-A

56804890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104793759-C-T

http://identifiers.org/hco/1/GRCh38#56805060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104793565-C-A

56805103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104793521-G-A

56805180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104793443-A-G

http://identifiers.org/hco/1/GRCh38#56805286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104793318-C-A

56805286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104793318-C-T

56805376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104793258-T-C

56805463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104793171-T-C

56805474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104793160-A-G

56805490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104793144-G-C

56805512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104793134-A-G

56805533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104793113-G-A

56805612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104793034-G-A

56806133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104792925-T-C

56806176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104792885-G-A

56806222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104792836-G-C

56806383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104792724-T-C

56806553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104792407-T-C

56806575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104792346-C-T

56807352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104791356-C-T

56807455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104791278-A-G

56807467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104791266-G-C

56807644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104791051-G-A

56807660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104791031-G-T

56807675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104791016-A-T

56807718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104790977-C-T

56807880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104790828-A-G

http://identifiers.org/hco/1/GRCh38#56808105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104790302-C-A

56808165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104790222-G-A

56808306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104790095-C-T

http://identifiers.org/hco/1/GRCh38#56808348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104790054-A-C

56808349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104790053-C-G

56808355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104790047-G-A

56808678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104789354-G-A

http://identifiers.org/hco/1/GRCh38#56809927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104789082-A-C

56809990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104789020-G-A

56810155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104788936-T-C

56810167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104788924-A-G

http://identifiers.org/hco/1/GRCh38#56810199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104788892-A-C

56810199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104788892-A-G

56810225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104788864-G-A

http://identifiers.org/hco/1/GRCh38#56812457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104778241-A-C

http://identifiers.org/hco/1/GRCh38#56812965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104777756-A-C

56813061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104777677-C-G

56813061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104777677-C-T

56813687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104777444-T-C

http://identifiers.org/hco/1/GRCh38#56813688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104777443-C-A

56813688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104777443-C-T

56814127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104777035-G-A

56814162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104777002-A-G

56814226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104776953-A-G

56814469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104776745-G-A

56814510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104776711-A-G

56814540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104776683-A-G

56814594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104776631-T-C

56814637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104776590-T-C

56814901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104776173-T-C

56814967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104776115-C-T

http://identifiers.org/hco/1/GRCh38#56815057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104776023-C-A

56815104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104775980-C-T

http://identifiers.org/hco/1/GRCh38#56815128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104775948-C-A

56815248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104775845-G-A

56815248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104775845-G-T

56815374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104775733-T-C

56815511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104775605-T-C

56815599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104775538-G-A

56815615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104775522-A-G

56816154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774378-T-G

56816222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774311-G-A

56816265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774269-T-G

56816302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774233-T-G

56816336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774199-G-T

56816521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104774028-T-G

56816547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104773996-G-T

56816558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104773986-C-T

56816619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104773937-C-T

56817262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104773030-C-T

56817389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104772906-C-T

56817429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104772869-C-T

56817463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104772836-T-G

56817507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104772790-G-C

56817538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104772759-G-A

56817637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104772552-T-C

56817654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104772521-T-C

56817750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104772421-G-T

56817843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104772338-C-T

56818089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104772070-T-G

56818136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104772011-C-T

56818154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104771993-T-C

56818209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104771918-G-A

56818287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104771762-A-G

56818497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104771584-C-T

56818653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104771452-G-C

http://identifiers.org/hco/1/GRCh38#56819157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#104770994-A-C

56819157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 104770994-A-G

56819186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104770972-C-T

56819217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 104770938-G-A

56819314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104770853-G-T

56819344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104770823-T-A

56819349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104770818-G-A

http://identifiers.org/hco/1/GRCh38#56819403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104770766-A-C

56819418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104770751-G-T

http://identifiers.org/hco/1/GRCh38#56819491-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#104770686-A-C

56819491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 104770686-A-G

56819500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104770677-G-T

56819521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104770665-G-A

56819521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104770665-G-T

56819524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104770662-G-A

56819742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron variant
orthologous variants: 104770439-T-C

http://identifiers.org/hco/1/GRCh38#56819769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104770412-C-A

http://identifiers.org/hco/1/GRCh38#56819777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104770404-C-A

http://identifiers.org/hco/1/GRCh38#56819797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104770384-C-A

http://identifiers.org/hco/1/GRCh38#56819809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104770372-A-C

56819809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron variant
orthologous variants: 104770372-A-G

56819843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron variant
orthologous variants: 104770343-G-T

56823647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron variant
orthologous variants: 104763057-G-A

56823750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104762521-G-A

56823750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104762521-G-T

http://identifiers.org/hco/1/GRCh38#56823952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104762319-C-A

56824042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104762231-T-C

http://identifiers.org/hco/1/GRCh38#56824277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#104762007-C-A

56824277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27295
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 104762007-C-T