20359232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119085861-G-T

http://identifiers.org/hco/16/GRCh38#20359254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119085883-A-C

20359254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119085883-A-G

http://identifiers.org/hco/16/GRCh38#20359385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119086013-C-A

20359385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119086013-C-G

20359386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119086014-A-G

20359395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119086020-T-C

20359413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119086038-T-A

20359413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119086038-T-C

20359422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119086047-G-A

20359591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119086240-A-G

20359594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119086243-A-T

20359642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119086277-G-A

20359642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119086277-G-T

20359843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119086440-C-T

20359887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119086485-G-A

20359887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119086485-G-T

20360053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119086631-A-G

20360136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119086717-A-G

20360221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119086804-G-A

20360221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119086804-G-T

20360324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119086918-C-G

20360425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087001-T-G

http://identifiers.org/hco/16/GRCh38#20360441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119087017-C-A

20360441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087017-C-G

20360441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087017-C-T

20360467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087046-C-T

20360561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119087145-C-G

20360664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119087248-T-A

20360664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119087248-T-G

20360675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087259-C-G

20360675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087259-C-T

20360678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087262-G-A

20360678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087262-G-T

20360682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087266-A-G

20360682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087266-A-T

20360741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087324-T-C

http://identifiers.org/hco/16/GRCh38#20360749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119087332-C-A

20360749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087332-C-T

20360764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087346-A-G

20360808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087393-G-A

20360994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087561-T-C

20361571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087807-A-G

20361657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087876-G-A

20361745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119087958-C-G

20362145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119088364-C-T

20362225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119088449-G-C

20362280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119088486-A-G

20362358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119088551-T-C

20362382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119088572-G-A

20362599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119088785-A-G

http://identifiers.org/hco/16/GRCh38#20362658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119088838-C-A

20362658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119088838-C-G

20362658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119088838-C-T

20362726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119088895-G-T

20362727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119088896-A-T

http://identifiers.org/hco/16/GRCh38#20363605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119089174-A-C

20364006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119089553-T-A

20364270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119089816-C-G

20364270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119089816-C-T

20364508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119089984-C-G

20364690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119090127-C-T

20364691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119090128-G-A

20364716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119090152-G-A

20364860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119090282-T-C

20364976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119090397-G-A

20365272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119090739-T-C

20365272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119090739-T-G

20365298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119090765-G-T

http://identifiers.org/hco/16/GRCh38#20365310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119090777-C-A

20365310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119090777-C-G

20365310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119090777-C-T

http://identifiers.org/hco/16/GRCh38#20365340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119090794-A-C

20365340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119090794-A-G

20365560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119091012-G-A

20365570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119091027-T-C

20365580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119091037-G-C

20365610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119091065-G-T

20365644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119091094-T-A

20365644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119091094-T-C

20365655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119091105-C-T

20365736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119091185-G-T

20365737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119091186-G-T

20367367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119092380-T-C

20367427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119092433-T-A

20367427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119092433-T-G

20367651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119092670-T-C

20367652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119092671-G-T

20367671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119092690-G-A

20368147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119093256-G-A

20368244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119093350-G-T

http://identifiers.org/hco/16/GRCh38#20368319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119093408-C-A

20368483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119093544-A-G

20368603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119093651-G-A

20368603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119093651-G-C

20368603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119093651-G-T

http://identifiers.org/hco/16/GRCh38#20368947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119093710-C-A

20369161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119093858-A-G

20369286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119093961-A-G

20369365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119094046-T-C

20369365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119094046-T-G

20369458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119094109-G-T

20369462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119094113-T-C

20369480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119094131-G-T

20369482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119094133-A-G

20369541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119094192-T-C

20369574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119094225-G-A

20369725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119094377-C-T

http://identifiers.org/hco/16/GRCh38#20369797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119094451-C-A

20369832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119094472-G-A

20369832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119094472-G-T

20369960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119094585-T-C

20370029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119095060-G-A

20370330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119095308-T-C

20370352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119095323-A-G

http://identifiers.org/hco/16/GRCh38#20370379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119095348-C-A

20370379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119095348-C-T

20370400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119095369-G-T

20371154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119095539-T-A

20371154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119095539-T-C

20371159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119095544-G-A

20371159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119095544-G-C

20371559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119095968-A-G

20371671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119096066-T-C

20371698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119096093-G-A

20371712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119096107-T-A

20371712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119096107-T-C

20371733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119096323-A-T

20371885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119096460-T-A

20372183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119096642-C-T

20372567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119096959-T-C

20372567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119096959-T-G

20372593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119096976-G-A

http://identifiers.org/hco/16/GRCh38#20372669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119097047-C-A

20372669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119097047-C-G

20372669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119097047-C-T

http://identifiers.org/hco/16/GRCh38#20372689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119097069-C-A

20372689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119097069-C-T

20372701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119097081-G-T

20372947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119097326-A-G

20372962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119097341-C-T

http://identifiers.org/hco/16/GRCh38#20372997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119097371-C-A

20372997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119097371-C-T

20373045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119097419-G-A

20373166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119097540-G-T

20373208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119097616-T-A

20373250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119097658-T-C

http://identifiers.org/hco/16/GRCh38#20373378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119097738-C-A

20373421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119097771-T-A

http://identifiers.org/hco/16/GRCh38#20373494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119097844-A-C

20374836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 119099609-G-C

20374976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119099749-G-A

http://identifiers.org/hco/16/GRCh38#20375000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119099773-C-A

20375000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119099773-C-G

20375038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119099811-T-C

20375166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119099937-A-G

20375337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100124-T-A

20375457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100236-G-A

20375476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100255-T-C

20375496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100275-A-T

http://identifiers.org/hco/16/GRCh38#20375587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119100366-A-C

20375593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100372-G-A

20375595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100374-A-G

20375822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100535-T-C

20375842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100555-T-A

20375863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100575-T-G

20375954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100708-A-G

20375954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100708-A-T

20376030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100778-T-C

20376036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119100784-G-C

20376060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119100808-C-T

20376122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119100870-C-T

20376206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119100954-A-T

20376297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119101013-T-C

20376333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119101047-G-T

20376626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119101311-A-G

20376714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119101388-T-A

20376714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119101388-T-C

20376714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119101388-T-G

20376744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119101424-G-A

20376764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119101444-C-T

20376878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119101548-G-A

20376878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119101548-G-C

20380830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119110381-T-G

20380853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119110404-G-A

20380929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119110471-C-T

http://identifiers.org/hco/16/GRCh38#20380994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119110541-C-A

20380994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119110541-C-T

20381085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119110634-T-A

20382352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119111212-C-T

20382496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119111530-A-T

20382693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119111716-G-A

20382954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119111930-C-T

20383203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119112158-C-G

20383349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119112305-C-G

20383349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119112305-C-T

http://identifiers.org/hco/16/GRCh38#20383727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119112764-A-C

20383757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119112796-T-C

http://identifiers.org/hco/16/GRCh38#20383925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119113195-C-A

http://identifiers.org/hco/16/GRCh38#20383943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119113214-A-C

20383943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119113214-A-G

20384049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119113457-G-A

20384119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119113579-T-C

20384268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119113750-C-T

20384423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119113894-G-A

20384501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119113955-G-A

20384501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119113955-G-T

20384528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119113981-T-G

20384539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119113992-G-A

20384539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119113992-G-T

20384562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114013-G-A

20384562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114013-G-T

http://identifiers.org/hco/16/GRCh38#20384569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119114020-C-A

http://identifiers.org/hco/16/GRCh38#20384575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119114026-C-A

20384575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114026-C-T

20384591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114042-G-A

20384611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114064-G-A

20384611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114064-G-T

20384633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114085-A-G

20384733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 119114185-C-T

http://identifiers.org/hco/16/GRCh38#20384855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119114307-A-C

20384893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114341-C-G

20384893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114341-C-T

http://identifiers.org/hco/16/GRCh38#20384944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119114384-C-A

20384944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114384-C-T

20384948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114388-T-C

http://identifiers.org/hco/16/GRCh38#20385292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119114623-A-C

http://identifiers.org/hco/16/GRCh38#20385909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#119114837-A-C

20385926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119114854-G-T

20386003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 119114903-G-C

20386014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119114910-G-A

20386014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 119114910-G-T

20386072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114962-A-G

20386089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114989-C-G

20386089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114989-C-T

20386097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119114997-C-G

20386301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119115178-G-A

20386447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119115298-G-T

20386539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119115370-G-A

20386550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119115381-C-G

http://identifiers.org/hco/16/GRCh38#20386618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119115453-C-A

20386618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119115453-C-G

20386618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119115453-C-T

20386634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 119115469-A-G

20386912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119115694-A-T

http://identifiers.org/hco/16/GRCh38#20391390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#119117288-C-A

20391533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119117433-G-A

20391533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119117433-G-T

20391787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119117706-T-G

20391802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119117716-G-A

20391802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119117716-G-C

20392041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119117927-G-T

20392567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119118407-C-T

20392694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119118532-T-G

20399054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119118821-G-A

20399054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119118821-G-C

20399054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119118821-G-T

20403955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119121960-C-G

20403955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119121960-C-T

20404057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119122068-T-C

20404123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119122155-C-G

20404123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119122155-C-T

20404430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119122412-G-A

20404430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 119122412-G-T

20404525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119122506-T-C

20404608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119122575-A-G

20404715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119122683-A-G

20404723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119122691-C-G

20404723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27338
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 119122691-C-T