http://identifiers.org/hco/1/GRCh38#54780524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106497431-A-C

54780524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497431-A-G

54780527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497428-T-A

54780527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497428-T-C

54780535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497420-G-A

54780535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497420-G-C

54780572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497394-A-G

54780675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497293-G-T

54780700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497268-G-T

54780721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497248-C-T

http://identifiers.org/hco/1/GRCh38#54780734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106497236-C-A

54780734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497236-C-T

54780741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497229-G-A

54780741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497229-G-T

54780742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497228-C-T

54780846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497155-G-C

54780846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497155-G-T

54780872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497129-G-A

54780909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106497108-G-T

54781047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106496976-T-C

http://identifiers.org/hco/1/GRCh38#54781115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106496898-C-A

54781115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106496898-C-T

54781192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106496704-G-A

54781192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3 prime UTR variant
orthologous variants: 106496704-G-T

54781292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense variant
orthologous variants: 106496610-T-C

54781292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense variant
orthologous variants: 106496610-T-G

54781379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense variant
orthologous variants: 106496523-G-A

54781379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense variant
orthologous variants: 106496523-G-C

54781379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense variant
orthologous variants: 106496523-G-T

http://identifiers.org/hco/1/GRCh38#54781469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106496433-C-A

54781469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense variant
orthologous variants: 106496433-C-T

54781478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense variant
orthologous variants: 106496424-T-C

http://identifiers.org/hco/1/GRCh38#54781593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106496309-A-C

54781607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106496295-G-A

54781607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106496295-G-T

54781643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106496259-A-G

54781691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106496211-T-C

54782203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106495884-T-G

http://identifiers.org/hco/1/GRCh38#54782282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106495840-A-C

http://identifiers.org/hco/1/GRCh38#54782542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106495604-C-A

54782542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106495604-C-T

http://identifiers.org/hco/1/GRCh38#54782568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106495570-C-A

54782568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106495570-C-T

54782587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106495551-G-T

54782662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106495443-A-G

54782735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106495374-A-G

54784227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106494942-G-A

http://identifiers.org/hco/1/GRCh38#54784427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106494788-A-C

http://identifiers.org/hco/1/GRCh38#54784454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106494761-C-A

54784454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106494761-C-T

http://identifiers.org/hco/1/GRCh38#54784476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106494744-C-A

54784476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106494744-C-T

54784641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106494604-C-T

54784652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106494593-G-A

http://identifiers.org/hco/1/GRCh38#54784653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106494592-A-C

54784653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106494592-A-G

54784707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106494558-G-C

54784746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106494519-G-A

54784769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106494493-G-A

54784769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 106494493-G-T

54784852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106494401-G-A

54784852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106494401-G-T

54784855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106494398-G-T

54784873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106494380-G-A

54784876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106494377-G-A

54784876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106494377-G-T

http://identifiers.org/hco/1/GRCh38#54784919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106494335-C-A

54784919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106494335-C-T

54784925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106494328-G-T

54785865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106494153-G-A

54785865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106494153-G-T

http://identifiers.org/hco/1/GRCh38#54785869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106494149-C-A

54785869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106494149-C-G

54785987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106494055-G-C

http://identifiers.org/hco/1/GRCh38#54786059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493983-A-C

54786059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106493983-A-G

54786065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106493977-A-G

54786075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106493967-T-C

54786079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106493963-C-T

54786128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106493914-T-C

54786156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493886-A-G

54786241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493851-C-G

54786241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493851-C-T

http://identifiers.org/hco/1/GRCh38#54786245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493847-C-A

54786245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493847-C-T

http://identifiers.org/hco/1/GRCh38#54786333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493773-C-A

54786333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493773-C-G

http://identifiers.org/hco/1/GRCh38#54786367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493739-C-A

54786367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493739-C-T

54786395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493725-T-A

http://identifiers.org/hco/1/GRCh38#54786447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493710-A-C

54786447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493710-A-G

54786472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493686-G-A

54786472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493686-G-T

54786478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493680-G-T

http://identifiers.org/hco/1/GRCh38#54786484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493674-A-C

54786484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493674-A-G

http://identifiers.org/hco/1/GRCh38#54786485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493673-C-A

http://identifiers.org/hco/1/GRCh38#54786506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493656-A-C

54786506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493656-A-G

54786506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493656-A-T

http://identifiers.org/hco/1/GRCh38#54786534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493629-C-A

54786534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493629-C-G

54786534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493629-C-T

54786571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493592-G-A

54786571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493592-G-C

54786571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493592-G-T

54786661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493502-G-A

54786661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493502-G-C

54786665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493498-A-G

54786665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493498-A-T

http://identifiers.org/hco/1/GRCh38#54786667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493496-A-C

54786667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493496-A-G

54786667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493496-A-T

54786672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493491-G-T

54786710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493455-T-C

54786715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493450-G-A

54786715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493450-G-T

54786716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493449-G-T

54786741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493424-G-A

54786741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493424-G-T

54786753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493412-G-A

54786753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493412-G-T

54786754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493411-G-A

54786754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493411-G-T

http://identifiers.org/hco/1/GRCh38#54786767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493398-C-A

http://identifiers.org/hco/1/GRCh38#54786773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493392-A-C

54786812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493342-G-A

54786812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493342-G-T

54786892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493266-G-A

54786892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106493266-G-T

54786996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106493171-G-A

54786996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 106493171-G-T

http://identifiers.org/hco/1/GRCh38#54787039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493128-C-A

54787039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106493128-C-T

54787096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106493074-A-G

54787108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106493062-A-G

http://identifiers.org/hco/1/GRCh38#54787144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493016-A-C

http://identifiers.org/hco/1/GRCh38#54787147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106493010-C-A

54787147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106493010-C-T

54787156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106492998-A-G

http://identifiers.org/hco/1/GRCh38#54787263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106492925-C-A

54787270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106492918-G-A

54787270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106492918-G-T

54787676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106491761-G-A

http://identifiers.org/hco/1/GRCh38#54787677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106491760-A-C

54787677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106491760-A-G

54787679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106491755-G-T

http://identifiers.org/hco/1/GRCh38#54787680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106491754-C-A

54787680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106491754-C-T

http://identifiers.org/hco/1/GRCh38#54787699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106491736-C-A

54787699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106491736-C-G

54787740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106491695-A-G

54787740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106491695-A-T

54787865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106491579-C-T

54787939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106491524-C-T

http://identifiers.org/hco/1/GRCh38#54787956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106491509-C-A

54787956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106491509-C-T

54787973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106491492-C-T

http://identifiers.org/hco/1/GRCh38#54787987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106491481-C-A

54787987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106491481-C-T

http://identifiers.org/hco/1/GRCh38#54787995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106491473-C-A

54787995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106491473-C-T

54788090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, start_lost
orthologous variants: 106491371-A-G

54788090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, start_lost
orthologous variants: 106491371-A-T

54788109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106491353-G-C

54788126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106491332-C-T

54788195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106491267-A-G

http://identifiers.org/hco/1/GRCh38#54788221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106491242-A-C

54788267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106491211-C-G

54788267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106491211-C-T

54788321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106491148-G-T

54788339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106491130-A-G

54788361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106491105-T-A

54788361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106491105-T-C

54788434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106491035-G-C

http://identifiers.org/hco/1/GRCh38#54788436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106491033-C-A

http://identifiers.org/hco/1/GRCh38#54788699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106490763-C-A

54788699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106490763-C-T

http://identifiers.org/hco/1/GRCh38#54789250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106490309-C-A

54789250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106490309-C-T

54789377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106489968-G-A

54789413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106489928-A-G

54789489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106489751-G-A

54789674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106489587-G-A

54789720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106489527-C-T

54789855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106489392-G-T

54789959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106489292-T-G

54790014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106489242-G-C

54791510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106488889-G-T

54791593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106488828-C-T

54791689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106488769-T-A

54791714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106488744-C-T

54791861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106488539-G-A

54791887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106488513-A-G

54791956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106488452-C-T

54791995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106488424-A-G

54792045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106488386-A-G

54792077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106488347-A-T

54792336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106488126-A-G

http://identifiers.org/hco/1/GRCh38#54792863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106487931-C-A

54792875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106487919-T-A

54792875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106487919-T-C

54792960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106487849-G-T

54792989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106487836-T-C

http://identifiers.org/hco/1/GRCh38#54793234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106487654-C-A

54793398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106487514-G-A

54793460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106487447-G-C

54794052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106486751-A-G

http://identifiers.org/hco/1/GRCh38#54794100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106486717-A-C

54794100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106486717-A-G

54794238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106486605-G-A

54794466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106486461-T-C

54794471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106486455-A-G

http://identifiers.org/hco/1/GRCh38#54794777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106486187-C-A

54794777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106486187-C-T

54794841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106486122-T-C

54794895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106486101-G-A

54794944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106486048-G-A

54794944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106486048-G-T

54795032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106486020-G-A

54795032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106486020-G-T

54795765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106485425-G-A

54795914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106485296-T-A

54796218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106484887-G-A

54796477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106484623-G-A

54796477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106484623-G-C

54796515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106484587-A-T

54797255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106484050-T-C

54797298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 106484007-T-G

54797754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106483758-T-C

54798149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106483389-A-G

54798181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106483353-T-G

54798937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106482565-T-C

54798939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106482563-A-G

54799268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106482362-C-T

54799272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106482358-C-T

54799300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106482328-C-T

54799328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106482296-G-A

http://identifiers.org/hco/1/GRCh38#54799329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106482295-C-A

54799471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106482155-C-T

54799547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106482086-G-A

54799590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106482043-C-T

54799648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106481991-G-A

54799953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106481718-C-T

54800095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106481582-C-T

54800478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106480365-A-G

54800480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106480363-G-A

54800480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106480363-G-C

54800480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: 106480363-G-T

http://identifiers.org/hco/1/GRCh38#54800521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106480358-C-A

http://identifiers.org/hco/1/GRCh38#54800676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#106480233-C-A

54800676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense variant
orthologous variants: 106480233-C-T

54800694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, undefined
orthologous variants: 106480215-T-G

54800792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: synonymous variant
orthologous variants: 106480117-T-A

http://identifiers.org/hco/1/GRCh38#54800832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#106480077-C-A

54800832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, undefined
orthologous variants: 106480077-C-T

54800859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense_variant, undefined
orthologous variants: 106480050-G-C

54800978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: synonymous variant
orthologous variants: 106479931-G-A

54800981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: synonymous variant
orthologous variants: 106479928-G-A

54800981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: synonymous variant
orthologous variants: 106479928-G-C

54801005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: synonymous_variant, undefined
orthologous variants: 106479904-C-T

54801054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: stop gained
orthologous variants: 106479855-G-T

54801114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: missense variant
orthologous variants: 106479795-T-C

54801212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106479709-G-C

54801212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106479709-G-T

54801221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5 prime UTR variant
orthologous variants: 106479700-G-T

54801226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5 prime UTR variant
orthologous variants: 106479696-G-A

54801227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5 prime UTR variant
orthologous variants: 106479695-G-A

54801227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5 prime UTR variant
orthologous variants: 106479695-G-T

54801242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5 prime UTR variant
orthologous variants: 106479680-G-A

54801242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26067
most severe consequence: 5 prime UTR variant
orthologous variants: 106479680-G-T