http://identifiers.org/hco/15/GRCh38#53513853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74192316-A-C

53513914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74192231-G-A

53514042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74192112-G-A

http://identifiers.org/hco/15/GRCh38#53514264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74191887-A-C

53514350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74191805-A-G

53514597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74191580-A-G

53514716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74191463-T-C

http://identifiers.org/hco/15/GRCh38#53514758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74191424-C-A

53514788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74191379-T-C

53514872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74191307-A-G

53514996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74191190-T-C

53515074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74191177-T-C

53515076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74191175-T-C

53515225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74191060-A-G

53515345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74190979-G-A

53515738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74190588-A-T

http://identifiers.org/hco/15/GRCh38#53515993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74190350-C-A

53515993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74190350-C-G

http://identifiers.org/hco/15/GRCh38#53516038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74190323-C-A

53516208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74190186-C-T

53516394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74189991-A-T

53516414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74189972-C-G

http://identifiers.org/hco/15/GRCh38#53516420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74189966-C-A

53516420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74189966-C-G

53516456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74189939-T-C

53516664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74189893-T-C

53516780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74189795-G-A

53517416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74189244-T-C

53517612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74189093-A-G

53517915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188841-C-G

53518102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188666-T-A

53518366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188403-T-C

53518516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188228-T-C

53518651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188097-C-T

http://identifiers.org/hco/15/GRCh38#53518691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74188059-C-A

53518691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188059-C-T

53518727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74188023-T-C

http://identifiers.org/hco/15/GRCh38#53518777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74187973-A-C

53519489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74186987-G-T

53519860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74186623-C-T

53520367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74186126-G-T

53520387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74186106-G-T

53520615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74185902-C-T

53520804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74185712-C-T

http://identifiers.org/hco/15/GRCh38#53521167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74185345-C-A

53521594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184921-C-T

53521706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184819-G-T

53521960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184569-G-A

53522334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184199-A-G

53522417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74184117-T-C

http://identifiers.org/hco/15/GRCh38#53522774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74183768-A-C

53522947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74183587-C-G

http://identifiers.org/hco/15/GRCh38#53523085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74183449-A-C

53523227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74183311-C-G

53523227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74183311-C-T

http://identifiers.org/hco/15/GRCh38#53523402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74183144-C-A

53523402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74183144-C-T

53523422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74183124-T-A

53523495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74183053-C-T

53523884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74182660-G-T

53524142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74182396-C-T

53524367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74181581-A-G

53524470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74181499-T-C

53524615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74181381-A-G

53524862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74181080-T-C

53524939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74181003-T-C

53525377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74180605-A-G

53525439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74180535-T-A

53525439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74180535-T-C

53525448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74180526-C-T

53525493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74180481-G-A

53525593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74180076-T-C

http://identifiers.org/hco/15/GRCh38#53525672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74180010-C-A

53525894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74179790-A-T

53526295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74179387-A-G

53526295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74179387-A-T

53526514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74179175-T-C

53526998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74178661-G-A

53527185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74178243-G-A

53527185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74178243-G-T

53527191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74178237-T-C

53527257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74178171-C-T

53528680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74173892-C-T

53530277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74172228-C-T

53530393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74172069-A-G

http://identifiers.org/hco/15/GRCh38#53530507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74171957-C-A

53530614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74171865-G-T

53530672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74171807-G-A

53530781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74171691-G-A

53530819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74171630-C-T

53532019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74170343-T-C

http://identifiers.org/hco/15/GRCh38#53535358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74168398-A-C

53535370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74168386-G-A

53535370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74168386-G-C

53536707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74166224-T-C

53536811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74166147-G-A

53537022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74165963-T-A

53537138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74165847-G-C

53537276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74165709-C-T

53537498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74165494-T-A

53537672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74165328-T-G

53537680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74165320-A-G

53537991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74165029-T-A

53538002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74165018-G-C

53538008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74165012-T-C

53538042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74164978-A-G

http://identifiers.org/hco/15/GRCh38#53538051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74164969-A-C

53538079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74164942-A-G

53538140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74164889-A-G

http://identifiers.org/hco/15/GRCh38#53538164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74164871-C-A

53548066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74162373-T-A

53548427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74162044-A-T

53548611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74161644-G-C

53548997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74161301-G-A

53549219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74161092-G-A

53549308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74161005-G-T

53549350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74160973-A-G

53549533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74160795-C-G

http://identifiers.org/hco/15/GRCh38#53549539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74160789-A-C

53549539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74160789-A-T

53550689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74159785-G-T

http://identifiers.org/hco/15/GRCh38#53550854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74159601-C-A

53550854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74159601-C-T

53551184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74159322-G-T

53551493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74158715-A-G

53551995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74158216-G-A

53552305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74157951-A-T

53552325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74157932-T-C

53552474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74157780-G-A

53552807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74157460-C-G

53553127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74157139-G-A

53553171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74157092-T-C

53553231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74157030-C-T

53553755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74156544-G-A

http://identifiers.org/hco/15/GRCh38#53553896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74156389-A-C

53554014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74156281-C-G

53554488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74155836-A-G

53554495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74155829-A-T

53554751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74155592-G-A

53554751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74155592-G-T

53554836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74155498-T-A

53555312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74155189-G-A

53555426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74155097-G-C

53555910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74153626-A-G

53556331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74153398-T-A

53556662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74153064-C-G

http://identifiers.org/hco/15/GRCh38#53556831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74152915-C-A

53556831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74152915-C-T

53556863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74152859-C-T

53556915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74152612-T-C

53556985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74152432-C-T

53557058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74152365-A-T

53557230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74152220-A-T

53557236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74152214-G-A

53557554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74151770-C-T

http://identifiers.org/hco/15/GRCh38#53557587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74151744-A-C

53557588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74151743-G-A

53557992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74150874-T-A

53558121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74150763-C-T

53558391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74150249-G-A

53558429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74150211-C-G

53558429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74150211-C-T

53558436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74150204-T-C

53558446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74150194-T-C

53558594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74150046-A-G

53558688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74149954-G-A

53558824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74149845-G-C

53559202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74149415-C-T

53559606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74148806-T-C

53559630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74148782-C-G

53559682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74148730-G-A

53559847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74148566-G-C

53559933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74148492-T-C

53560000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74148435-G-A

53560035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74148400-T-C

53560118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74148313-A-T

53560156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74148273-T-C

53562626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74147909-T-C

53562666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74147869-T-C

53562721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74147821-T-G

53562875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74147676-A-G

53562943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74147610-A-T

53562961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74147592-G-A

53563233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74147327-C-G

53563664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74147034-C-T

53566605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74144748-A-G

53566739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74144623-C-T

53566957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74144411-T-C

53567038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74144329-T-C

53567038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74144329-T-G

53567229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74144135-G-T

53567839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74143403-C-T

53567972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74143277-G-T

53568001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74143249-G-A

53568001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74143249-G-T

http://identifiers.org/hco/15/GRCh38#53568106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74143144-C-A

53568106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74143144-C-T

53568149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74143103-T-C

http://identifiers.org/hco/15/GRCh38#53575184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74141494-A-C

53575211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74141471-C-T

53575449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74141234-G-A

53575512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74141169-A-G

53575619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74140821-T-C

53575882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74140539-G-A

53575932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74140500-C-T

53576018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74140415-T-C

53576092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74140341-A-G

53576093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74140340-G-A

53576138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74140294-C-G

53576162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74140269-C-T

53576347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74140092-T-A

53576347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74140092-T-C

53576947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74139747-T-C

53577060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74139661-T-C

53577588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74139159-A-G

53577894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74138423-G-A

53577957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74138365-G-T

53578256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74137778-C-T

53578289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74137751-T-C

53578292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74137748-G-A

53578298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74137742-T-C

http://identifiers.org/hco/15/GRCh38#53578323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74137717-C-A

53578323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74137717-C-T

53578443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74137603-T-C

53578443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74137603-T-G

53578461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74137585-T-C

53578498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74137549-T-C

53578592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74137497-G-C

53578681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74137409-T-A

53578682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74137408-C-G

53580246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74136120-A-G

53580526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74135815-G-C

53580549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74135792-G-A

53580549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74135792-G-T

53581167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74134957-G-A

53581167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74134957-G-C

53581250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74134834-A-T

53581659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74134184-G-C

53581668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74134175-A-T

53581691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74134152-G-C

http://identifiers.org/hco/15/GRCh38#53581853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74133792-A-C

53581862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74133783-T-A

53581862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74133783-T-C

53582661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74133013-T-G

53582875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74132790-A-G

53582936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74132733-A-T

53582950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74132719-A-T

53582967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74132702-A-G

53582967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74132702-A-T

53583050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74132566-T-A

53583050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74132566-T-C

http://identifiers.org/hco/15/GRCh38#53583091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74132493-C-A

53583193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74132395-T-C

53583447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74132135-A-G

53583591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74132037-T-C

53583591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74132037-T-G

53583696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74131934-C-T

53583881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74131748-T-C

53583898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74131731-C-T

http://identifiers.org/hco/15/GRCh38#53584394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74130977-C-A

53584431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74130949-C-T

53590830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74129008-G-A

53591020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74128892-G-C

53591057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74128847-A-G

http://identifiers.org/hco/15/GRCh38#53591131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74128773-A-C

53591131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74128773-A-G

53591293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74128560-G-A

53591319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74128534-A-G

53591393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74128466-A-T

53591765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74128229-G-A

53591805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74128202-T-C

53591807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74128200-T-G

53591946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74128068-G-A

http://identifiers.org/hco/15/GRCh38#53591976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74128038-A-C

53591976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74128038-A-G

53592091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74127919-A-G

53592110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74127902-T-A

53592355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74127672-A-G

53592364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74127655-G-A

53592440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74127577-G-A

53592862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74126640-T-C

53592976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74126528-C-T

53593155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74126349-T-C

53593174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74126330-G-A

53593186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74126318-A-G

http://identifiers.org/hco/15/GRCh38#53597102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74126029-A-C

53597140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74125991-T-C

53597234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74125897-T-A

53597296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74125834-G-A

53597296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74125834-G-T

53597384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74125753-G-A

http://identifiers.org/hco/15/GRCh38#53597411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74125726-C-A

53597411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74125726-C-G

53597411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74125726-C-T

53609325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124809-C-T

53609398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124731-G-A

53609398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124731-G-T

53609426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124690-T-C

53609436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124674-A-G

http://identifiers.org/hco/15/GRCh38#53609459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74124652-C-A

53609514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 74124598-T-C

53609514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 74124598-T-G

53609523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74124589-T-C

53609523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74124589-T-G

53609574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74124538-A-T

53609575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74124537-C-T

53609588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74124524-C-G

http://identifiers.org/hco/15/GRCh38#53609724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74124398-C-A

53609724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124398-C-G

53609724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124398-C-T

53609737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124385-T-C

53609738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124384-T-C

53609738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124384-T-G

53609756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124372-G-A

53609767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124356-G-A

53609981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124214-A-G

53609993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124204-C-T

53610108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74124098-A-G

http://identifiers.org/hco/15/GRCh38#53610450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74123766-C-A

53610450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74123766-C-T

53610568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74123655-T-C

53610592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74123627-A-G

53610597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74123622-T-G

53610633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74123576-G-T

53610701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74123510-T-C

53610801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74123418-T-G

53611108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74123114-C-T

53611535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74122531-C-T

53611627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74122297-G-A

53612004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74121920-G-A

53612082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74121858-G-A

53612154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74121787-T-C

53612225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74121719-T-G

53612637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74121402-G-A

53613568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120743-T-A

http://identifiers.org/hco/15/GRCh38#53613585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74120734-C-A

53613585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120734-C-T

http://identifiers.org/hco/15/GRCh38#53613590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74120729-C-A

53613590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120729-C-T

http://identifiers.org/hco/15/GRCh38#53613606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74120712-A-C

53613606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120712-A-T

http://identifiers.org/hco/15/GRCh38#53613630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74120688-A-C

53613630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120688-A-T

53613729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 74120589-T-A

53613774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120539-T-C

53613807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120507-T-C

53613828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120486-T-C

53613832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120482-G-C

53613832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120482-G-T

53613925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120407-C-T

http://identifiers.org/hco/15/GRCh38#53613975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74120394-C-A

53614055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120333-C-T

53614073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74120310-T-C

53614933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74118858-T-C

53615100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74118678-G-T

53615108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74118670-G-A

53615326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74118164-G-T

53615394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74118099-T-C

53615415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74118078-G-A

53615415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74118078-G-T

53615429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74118064-C-T

53615510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74117983-T-A

53615510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74117983-T-C

http://identifiers.org/hco/15/GRCh38#53615519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74117974-C-A

53615519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74117974-C-T

http://identifiers.org/hco/15/GRCh38#53615554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74117939-A-C

53615675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74117821-G-A

53615846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74117650-T-A

53615870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74117626-T-G

53615871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 74117625-G-A

53615963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74117533-T-G

53616137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74117359-A-G

53616137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74117359-A-T

http://identifiers.org/hco/15/GRCh38#53616357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74117153-A-C

53616358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74117152-A-T

53618192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74116462-C-T

53618375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74115774-C-T

53618446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74115715-C-T

53618527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74115627-T-C

53618580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74115570-C-G

53618580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74115570-C-T

53618984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74115377-T-G

53619351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74115186-G-C

53619363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74115174-T-G

53619398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74115141-A-G

53619525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74115026-G-C

53619595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74114932-T-C

53619726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74114813-C-T

53619774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74114766-T-C

53619957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74114587-G-A

53620128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74114431-T-A

53620201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74114358-T-C

53620392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74114171-T-C

53640287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74113198-T-A

53640346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74113139-C-T

53640678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74112839-A-G

53640781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74112760-A-T

53640790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74112751-T-C

http://identifiers.org/hco/15/GRCh38#53643097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74108777-A-C

53643153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74108734-A-G

53643490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74108411-T-G

53643890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74107040-A-G

53644007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74106925-T-C

53644148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74106787-G-A

53644148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74106787-G-T

53644214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74106683-C-G

53644214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74106683-C-T

http://identifiers.org/hco/15/GRCh38#53644786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74105929-A-C

53644899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74105819-A-T

53645070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74105648-G-A

53645200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74105518-T-C

53645543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74105205-T-C

53646335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74103634-T-A

53646370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74103604-A-G

53646499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74103337-A-G

53647725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74102409-A-G

http://identifiers.org/hco/15/GRCh38#53647935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74102235-C-A

53647942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74102228-T-G

53648444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74101789-A-G

53650002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74100615-T-C

53650044-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74100573-T-G

53650078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74100538-T-C

http://identifiers.org/hco/15/GRCh38#53650138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74100483-A-C

53650234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74100365-A-G

53650459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74100176-A-G

53652381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74099162-C-T

53652387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74099094-C-T

53652390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74099091-C-T

53652397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74099084-G-C

53652494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74098989-T-C

53652502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74098981-G-A

http://identifiers.org/hco/15/GRCh38#53652870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74098622-C-A

53654616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74098081-C-T

53654821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74097910-C-T

53654880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74097854-T-C

53655259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74097792-A-G

53655259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74097792-A-T

53655568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74097486-G-C

53655594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74097460-C-T

http://identifiers.org/hco/15/GRCh38#53655600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74097454-C-A

53655617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74097437-G-A

53655684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74097382-G-A

53655964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74097314-T-G

53656223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74097120-T-C

53656283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74097091-G-A

53656283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74097091-G-C

53656559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74096806-G-C

http://identifiers.org/hco/15/GRCh38#53656883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74096592-A-C

53656885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74096590-C-T

http://identifiers.org/hco/15/GRCh38#53657012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74096551-C-A

53657196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74096478-A-G

53657411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74096281-T-C

53657775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74095893-C-G

53658383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74095243-C-T

53658642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74094973-T-C

http://identifiers.org/hco/15/GRCh38#53659224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74094392-C-A

53659224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74094392-C-T

53659402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74094212-G-A

http://identifiers.org/hco/15/GRCh38#53660209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74093466-A-C

53660215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74093460-G-A

53660215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74093460-G-T

http://identifiers.org/hco/15/GRCh38#53661867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74090786-C-A

53661872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74090781-G-A

http://identifiers.org/hco/15/GRCh38#53662194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74090453-C-A

53662366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74090270-C-T

53663476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74089175-T-C

53664030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74088502-A-G

53664053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74088479-A-T

53664065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74088467-G-A

53664233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74088324-T-C

53664344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74088195-G-A

53664887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74087481-A-G

53664940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74087430-G-A

53665361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74087195-C-T

http://identifiers.org/hco/15/GRCh38#53665422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74087128-A-C

53665482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74087070-G-A

53665482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74087070-G-T

53665532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74087036-G-A

53666203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74086352-T-C

http://identifiers.org/hco/15/GRCh38#53666430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74086119-A-C

53666661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74085038-T-G

53666731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74084940-A-G

53667818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74084110-C-T

53667905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74084032-A-T

53667934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74084001-T-C

53668181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74083775-G-C

53669932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74082346-T-G

53669939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74082339-A-T

53670260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74081599-T-G

53670396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74081437-G-T

53670441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74081392-C-G

53670465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74081362-T-C

53670525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74081295-G-A

53671022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74080334-G-A

53671428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74079590-C-T

53671504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74079509-A-T

53671578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74079438-T-C

53671759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74079274-G-C

53671853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74079170-T-C

53672097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078987-T-C

53672191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078893-A-G

53672306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078772-G-A

53672306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078772-G-C

53672309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078769-G-A

53672309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078769-G-T

53672429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078660-A-G

53672434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078655-G-A

53672434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078655-G-C

53672491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078598-C-T

53672514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078563-C-T

53672702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078409-T-C

53673171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078259-T-C

53673176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078254-A-G

53673386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078040-C-G

53673426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74078000-T-G

53673648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74077825-T-G

53673675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74077797-G-A

53673675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74077797-G-C

53674059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74077748-T-C

53674187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74077622-G-C

53674254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74077552-T-G

53674788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74077017-C-G

53675571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74076533-T-C

53675581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74076524-A-G

53676186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74075969-C-G

53676276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74075880-A-G

53677378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74075086-G-T

53678145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74073714-G-C

53678145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74073714-G-T

53678330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74073543-A-G

53678407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74073480-T-C

53680979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74072683-C-G

53681112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74072559-T-C

http://identifiers.org/hco/15/GRCh38#53681453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74072241-C-A

53681455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74072239-G-A

53681455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74072239-G-C

53681553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74072141-C-T

53693037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74071245-A-T

53693096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74071186-C-G

53693296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74071023-T-C

53694218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74070309-T-G

53694320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74070232-T-C

53694371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74070193-T-C

53694733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74069843-T-G

53694928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74069000-G-A

53695136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74068808-C-T

http://identifiers.org/hco/15/GRCh38#53695150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74068794-C-A

53695256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74068667-T-C

53695560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74068378-G-A

53695560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74068378-G-T

http://identifiers.org/hco/15/GRCh38#53696387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74067809-C-A

53696469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74067741-G-A

53696529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74067675-T-C

53696674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74067523-A-T

http://identifiers.org/hco/15/GRCh38#53696743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74067450-A-C

53696889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74067147-C-T

53696961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74067055-C-T

http://identifiers.org/hco/15/GRCh38#53697133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74066896-C-A

53697133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74066896-C-T

53697240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74066746-T-C

53697293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74066698-T-A

53697548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74066493-G-A

53698274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74066107-T-C

http://identifiers.org/hco/15/GRCh38#53698358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74066024-A-C

http://identifiers.org/hco/15/GRCh38#53698513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74065874-C-A

53698920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74065533-G-A

53699180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74065306-G-T

53699697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74064779-T-A

53699697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74064779-T-C

53699719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74064760-A-G

53699942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74064537-T-C

http://identifiers.org/hco/15/GRCh38#53700074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74064421-C-A

53700245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74064245-A-G

53700465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74064028-C-T

53700835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74063615-T-G

53700836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74063614-G-A

53700885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74063565-G-A

53701941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74062607-T-C

http://identifiers.org/hco/15/GRCh38#53701949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74062599-A-C

53701998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74062550-C-T

53702127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74062431-G-A

53702127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74062431-G-T

53702207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74062346-T-G

53702549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74062049-G-T

53702563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74062035-G-T

53702573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74062025-C-T

53703641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74061546-G-A

53703674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74061495-C-T

53704835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74060078-T-A

53704843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74060070-T-C

53704867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74060047-G-A

53704867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74060047-G-C

53704867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74060047-G-T

http://identifiers.org/hco/15/GRCh38#53704873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74060041-A-C

53704873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74060041-A-T

http://identifiers.org/hco/15/GRCh38#53704894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74060020-A-C

53704910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74060004-A-G

http://identifiers.org/hco/15/GRCh38#53704987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74059935-C-A

53704987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 74059935-C-T

http://identifiers.org/hco/15/GRCh38#53705253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74059668-A-C

53705253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74059668-A-G

53705253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74059668-A-T

53705330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74059589-A-G

53705330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74059589-A-T

53705386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74059495-A-G

53705791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74059112-G-A

53705791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74059112-G-T

53705803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74059100-T-C

http://identifiers.org/hco/15/GRCh38#53705805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74059098-C-A

53705805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74059098-C-T

http://identifiers.org/hco/15/GRCh38#53705938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74058991-C-A

53706177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74058766-T-C

53706192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74058751-C-T

53706307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74058617-C-T

53706364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74058573-A-G

53706365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74058572-T-C

53706389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74058565-T-C

53706411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74058543-T-A

53706411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74058543-T-G

53706437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74058517-C-T

53706446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74058504-A-T

http://identifiers.org/hco/15/GRCh38#53706456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74058493-A-C

53708536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74058170-G-T

53708573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74058127-A-G

53709658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74057206-G-A

53709658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74057206-G-C

53709690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74057187-A-G

53709801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74057022-C-G

53709882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74056955-C-G

53710120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74056724-A-G

53710188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74056655-A-G

53710198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74056645-G-C

53710428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74056448-G-A

53710467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74056409-T-C

53710630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74056272-T-C

53710785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74056139-A-G

53710794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74056134-G-C

53710794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74056134-G-T

53710934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74056020-A-G

53711062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74055900-T-C

53711312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74055651-T-C

53711429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74055534-C-G

53711558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74055382-T-C

53711692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74055236-A-G

53711822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74055111-T-C

53711986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74054964-T-C

53712045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74054906-G-A

53712618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74054474-T-A

53712618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74054474-T-C

http://identifiers.org/hco/15/GRCh38#53712649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74054443-C-A

53712649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74054443-C-T

53712764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74054339-T-A

http://identifiers.org/hco/15/GRCh38#53712800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74054303-A-C

http://identifiers.org/hco/15/GRCh38#53712903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74054200-A-C

53712981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74054148-A-T

http://identifiers.org/hco/15/GRCh38#53712998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74054127-C-A

53712998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74054127-C-T

53713379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053913-A-G

53713379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053913-A-T

53713831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053820-C-T

53713938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053720-T-C

53714119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053575-G-A

53714144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053549-A-G

http://identifiers.org/hco/15/GRCh38#53714207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74053479-A-C

53714485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74053237-T-G

53714551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053167-T-G

53714557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053161-T-C

53714585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053136-T-C

53714602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053119-G-A

53714602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053119-G-C

53714602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053119-G-T

53714611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053110-A-G

53714661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053071-T-C

53714666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74053066-C-T

53714811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052946-T-C

53714892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052762-T-C

53714968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052681-C-T

53714969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052680-T-G

53715014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052640-C-T

53715050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052604-G-A

53715050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052604-G-T

53715061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052593-A-G

53715140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052522-G-A

53715140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052522-G-T

53715174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052497-G-A

53715261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74052414-C-T

53715463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052206-A-G

53715491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052178-G-A

53715491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052178-G-T

53715510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052164-G-A

53715510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74052164-G-T

53716251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74051196-G-A

http://identifiers.org/hco/15/GRCh38#53716300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74051163-A-C

53716573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74050875-C-T

53716614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74050839-G-A

53716614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74050839-G-T

53716633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74050820-G-T

53716715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74050739-T-C

53716781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74050658-A-G

53716817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74050617-A-G

53716823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74050611-T-C

53716847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74050587-A-G

53717167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74050116-C-T

53717395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74049835-T-C

53717609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74049371-G-T

53717838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74049182-C-G

53717838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74049182-C-T

53717955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74049048-G-A

53719357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74048489-T-C

53719463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74048393-T-C

53719463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74048393-T-G

53719516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74048341-G-A

http://identifiers.org/hco/15/GRCh38#53719747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74048124-C-A

53719822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74048055-C-T

53719978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74047884-A-T

53720020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74047834-G-A

53720049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74047808-G-T

53720063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74047794-G-T

53720139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74047711-T-C

53722783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74047032-G-A

53722789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74047026-A-G

53722791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74047024-A-T

http://identifiers.org/hco/15/GRCh38#53722823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74046992-A-C

http://identifiers.org/hco/15/GRCh38#53723074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74046711-C-A

53723125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74046661-G-T

53726938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74044761-A-G

53727026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74044650-G-A

53727026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74044650-G-C

http://identifiers.org/hco/15/GRCh38#53727052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74044626-C-A

53727465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74044255-T-C

53727465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74044255-T-G

53727473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74044247-C-G

53727481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74044239-T-C

http://identifiers.org/hco/15/GRCh38#53727535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74044189-C-A

53727535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74044189-C-T

53731131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74043586-G-C

http://identifiers.org/hco/15/GRCh38#53731175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74043535-C-A

53731379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74043336-C-T

53731380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74043335-A-T

53731715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74043044-T-A

53731741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74043018-G-A

53731754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74043005-C-G

53731834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74042943-C-G

53731950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74042830-T-C

53732061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74042723-G-A

53732089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74042697-T-C

53732946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74041891-G-T

53732950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74041887-G-A

53732950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74041887-G-C

53732950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74041887-G-T

http://identifiers.org/hco/15/GRCh38#53732976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74041880-A-C

53732976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74041880-A-G

53732980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74041876-C-T

53732981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74041875-A-G

53733184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74041668-A-G

53733192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74041660-T-A

53733192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74041660-T-C

http://identifiers.org/hco/15/GRCh38#53744995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74032378-C-A

53745066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74032310-A-T

53745117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74032259-C-G

53745117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74032259-C-T

http://identifiers.org/hco/15/GRCh38#53745125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74032251-C-A

53745174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74032205-T-G

53745190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74032189-G-A

53745204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74032175-G-A

http://identifiers.org/hco/15/GRCh38#53745338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74032047-A-C

53745351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74032034-T-C

53745351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74032034-T-G

53745494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74031901-A-G

53745708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74031301-A-G

53745724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74031285-G-A

53745730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74031279-C-T

53746377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74030610-T-C

53746506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74030486-T-C

53746708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74030300-T-G

53746757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74030253-T-C

53747036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74029743-G-C

53747095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74029679-G-A

53747095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74029679-G-T

53747470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74028482-G-T

53747547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74028403-C-T

53747576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74028373-A-G

53747782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74028189-G-T

53748030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74027745-T-C

53748097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74027642-G-C

53748097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74027642-G-T

53748320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74027420-T-A

53748354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74027386-C-T

53753483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74025259-G-T

53753511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74025228-T-A

53753569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74024559-T-A

53753737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74024400-G-A

http://identifiers.org/hco/15/GRCh38#53753872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74024267-A-C

53753872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74024267-A-T

53754119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74024058-G-A

http://identifiers.org/hco/15/GRCh38#53754130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74024048-A-C

53754182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74023988-C-T

53754336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74023847-G-A

53754484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74023751-G-A

53754485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74023750-T-C

53754883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74023357-G-A

53755172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74023067-C-G

53755216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74022966-T-A

53755244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74022938-C-G

53755303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74022876-T-C

53755527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74022668-T-C

53755656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74022554-T-C

53755656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74022554-T-G

53755667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74022542-C-T

53755963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74022252-A-G

53756660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74020210-C-T

53756690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74020181-A-G

http://identifiers.org/hco/15/GRCh38#53756792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74020088-C-A

53756792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74020088-C-T

53756798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74020083-T-C

53756919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74020008-A-G

53756919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74020008-A-T

53757690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74019390-T-C

53757740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74019315-C-T

53757814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74019247-A-G

http://identifiers.org/hco/15/GRCh38#53758811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26790
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#74018150-C-A