207821518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64828508-A-G

207821540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64828530-A-G

http://identifiers.org/hco/2/GRCh38#207821640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64828625-C-A

207821640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64828625-C-T

207822134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64828763-G-T

http://identifiers.org/hco/2/GRCh38#207822374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64828975-C-A

207822398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64828998-A-G

207822695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 64829264-T-C

http://identifiers.org/hco/2/GRCh38#207822920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64829462-C-A

207822920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64829462-C-T

207822927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64829469-G-A

207822941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64829483-T-C

207823019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64829563-A-G

207823053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64829583-C-G

207823070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64829600-T-G

207823097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64829627-T-C

207823852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64829881-G-A

207823852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64829881-G-T

207823861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64829890-A-G

207824007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830044-A-G

207824107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830116-A-G

207824112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830121-G-A

207824112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830121-G-T

207824119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830128-A-G

http://identifiers.org/hco/2/GRCh38#207824148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64830170-C-A

207824148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830170-C-G

207824159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830179-G-C

207824498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830497-G-A

207824498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830497-G-T

207824503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830502-T-C

207824556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830556-C-T

http://identifiers.org/hco/2/GRCh38#207824570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64830570-C-A

207824702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830717-A-G

207824813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830807-C-T

http://identifiers.org/hco/2/GRCh38#207824827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64830820-C-A

207824827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830820-C-T

http://identifiers.org/hco/2/GRCh38#207824933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64830921-A-C

http://identifiers.org/hco/2/GRCh38#207824950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64830938-C-A

207824950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830938-C-T

207825044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64830991-T-A

http://identifiers.org/hco/2/GRCh38#207825213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64831159-C-A

207825377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831319-A-G

207825384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831326-A-T

207825620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831525-G-T

207825648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831553-G-A

207825707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831615-G-A

207825805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831688-C-T

207825899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831774-G-A

207825939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831817-G-A

207825939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831817-G-C

207825939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831817-G-T

207825989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831866-G-A

207825989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831866-G-T

207826022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831890-C-T

207826066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64831925-G-T

207826453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64832310-G-A

207826622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64832465-G-A

207826622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64832465-G-T

http://identifiers.org/hco/2/GRCh38#207826731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64832545-C-A

207826731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64832545-C-G

207826731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64832545-C-T

207826734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64832548-G-T

207826910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64832721-T-A

207826976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64832793-C-T

http://identifiers.org/hco/2/GRCh38#207827001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64832818-C-A

207827243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64833230-T-C

207827290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64833278-G-T

207827407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64833385-G-A

207827430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64833408-A-G

207827451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64833430-G-T

http://identifiers.org/hco/2/GRCh38#207827489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64833465-A-C

207827489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64833465-A-G

207827564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64833541-A-G

http://identifiers.org/hco/2/GRCh38#207827580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64833556-C-A

207827610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64833592-T-C

http://identifiers.org/hco/2/GRCh38#207827662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64833633-C-A

207827662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64833633-C-G

207827982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64833896-G-C

207827998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64833912-A-T

207828090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64834003-G-T

207828134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64834046-G-A

207828134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64834046-G-T

http://identifiers.org/hco/2/GRCh38#207828162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64834077-A-C

207828162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64834077-A-G

207828162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64834077-A-T

207828168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64834083-T-C

http://identifiers.org/hco/2/GRCh38#207828248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64834151-C-A

http://identifiers.org/hco/2/GRCh38#207828250-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64834153-A-C

207828250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64834153-A-T

207828272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3 prime UTR variant
orthologous variants: 64834169-T-C

207828326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 64834203-T-C

207828328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 64834205-C-T

207828623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64834452-G-A

207828623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64834452-G-T

207828897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64834744-G-A

207829070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64834888-A-T

http://identifiers.org/hco/2/GRCh38#207831088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64836237-C-A

207831860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64836867-A-G

http://identifiers.org/hco/2/GRCh38#207831984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64836968-A-C

http://identifiers.org/hco/2/GRCh38#207833433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64840241-C-A

207833441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64840247-G-A

207833544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64840336-G-A

207833862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64840617-T-C

http://identifiers.org/hco/2/GRCh38#207833863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64840618-A-C

207834033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64840912-G-A

http://identifiers.org/hco/2/GRCh38#207834800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64841264-C-A

207834859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64841317-C-T

207836638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64841973-T-C

207836743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64842077-G-T

207836749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64842083-C-T

207836902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64842233-C-T

207836922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64842254-G-T

207836934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64842266-A-G

207836936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64842268-G-A

207837014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64842345-C-T

http://identifiers.org/hco/2/GRCh38#207837202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64842541-C-A

207837245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64842597-G-A

207838574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64843693-G-C

207839212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64844276-A-G

207844263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64845204-C-T

http://identifiers.org/hco/2/GRCh38#207844297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64845240-A-C

207844297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64845240-A-T

207844312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64845255-T-C

207844717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64845416-C-G

http://identifiers.org/hco/2/GRCh38#207844799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64845493-C-A

207844892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64845578-G-T

207844900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64845586-G-A

207844942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64845628-T-A

207845065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64845772-A-T

207845166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64845865-A-G

207845649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64846359-C-G

207845947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64846685-G-T

207846984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64847447-T-C

207847117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64847575-C-T

207847219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, undefined
orthologous variants: 64847643-G-A

207847511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, undefined
orthologous variants: 64848004-C-T

207847524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, undefined
orthologous variants: 64848008-C-T

207847608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64848078-A-G

207847782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, undefined
orthologous variants: 64848229-C-T

http://identifiers.org/hco/2/GRCh38#207848424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64848839-C-A

207848563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64849153-G-A

207848657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, undefined
orthologous variants: 64849254-C-T

207848678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64849275-G-T

http://identifiers.org/hco/2/GRCh38#207850785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64850530-C-A

207850793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64850538-T-G

207851222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64850638-T-C

207851354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64850752-T-C

207851361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64850755-G-T

207851441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64850828-A-G

207852139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64851119-T-C

207852145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64851125-G-A

207852145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64851125-G-T

207852663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64851829-A-G

207854766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, undefined
orthologous variants: 64852917-A-G

http://identifiers.org/hco/2/GRCh38#207855118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64853218-C-A

207855471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64853535-T-A

207855471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64853535-T-C

207855475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64853539-T-C

207855680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64853724-T-C

207855826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64854042-C-T

207856484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64854598-A-G

207856745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64854789-T-C

207856758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64854802-T-G

207856777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64854821-C-T

207860233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64856915-C-G

207860266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64856948-C-T

207860362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64857032-C-T

207860495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64857166-G-C

207860775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64857463-T-C

207860855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64857546-C-T

207860924-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64858927-T-A

207860939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64858942-A-G

207861050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64859042-G-A

207861050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64859042-G-C

207861064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64859056-A-G

207861209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 64859199-G-A

http://identifiers.org/hco/2/GRCh38#207861294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64859283-A-C

207862053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64860035-C-T

207862178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64860172-T-C

207864043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64860539-T-G

207864048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64860544-A-G

207864358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64860849-T-C

207865148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64861479-G-T

207865378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64861704-C-T

207866192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64862029-G-C

http://identifiers.org/hco/2/GRCh38#207866275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64862101-C-A

http://identifiers.org/hco/2/GRCh38#207866304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64862129-A-C

207866312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64862138-T-C

207866760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64862595-T-C

207866966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64862794-T-C

207866974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64862802-A-G

http://identifiers.org/hco/2/GRCh38#207867497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64863226-A-C

http://identifiers.org/hco/2/GRCh38#207867945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64863561-A-C

207868335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64864268-C-G

207868339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64864272-T-A

207868339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64864272-T-C

207868631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64864544-G-A

207868631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64864544-G-T

207868645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64864554-G-A

207868685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64864586-T-C

207868775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 64864673-C-T

207869075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64864882-G-A

207869075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 64864882-G-T

207869845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 64865579-T-C

http://identifiers.org/hco/2/GRCh38#207869869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64865602-C-A

207870000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64865728-T-A

http://identifiers.org/hco/2/GRCh38#207870419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#64866151-A-C

207870531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, undefined
orthologous variants: 64866254-A-G

207871414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64866887-G-C

207871639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64867077-T-C

207871676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64867108-G-A

207871717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64867141-G-A

207873215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64868301-G-A

207873772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64868827-A-G

207874071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64869133-C-T

207875341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64869681-A-G

207875981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64869859-A-G

207876264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64870065-A-G

207876787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64870537-A-G

207876888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64870725-C-G

207877219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64871053-G-T

207877347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64871147-C-G

207877439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64871207-C-T

207877515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64871265-G-A

207877524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64871271-G-C

207877524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64871271-G-T

207879493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64872511-G-A

207879533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64872551-C-T

207879565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64872582-G-T

207879677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, undefined
orthologous variants: 64872693-G-T

207879790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, undefined
orthologous variants: 64872786-T-C

http://identifiers.org/hco/2/GRCh38#207879817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64872813-A-C

207879898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64872890-A-G

207880128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64873007-C-T

207880142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64873021-C-G

http://identifiers.org/hco/2/GRCh38#207880781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64874239-A-C

http://identifiers.org/hco/2/GRCh38#207880810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64874268-A-C

http://identifiers.org/hco/2/GRCh38#207880824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64874282-C-A

http://identifiers.org/hco/2/GRCh38#207880890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64874341-C-A

207881444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64874826-G-A

http://identifiers.org/hco/2/GRCh38#207882634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64875607-C-A

207882634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64875607-C-G

207882634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64875607-C-T

207882640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64875613-T-G

207885923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64876514-C-T

207886042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64876656-T-G

http://identifiers.org/hco/2/GRCh38#207886784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64877699-C-A

207886821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64877732-G-A

207886957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64877863-G-A

207886993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64877897-T-A

207887224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64878074-C-T

http://identifiers.org/hco/2/GRCh38#207887502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64878342-C-A

207887636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64878472-T-C

207887820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64878655-G-C

http://identifiers.org/hco/2/GRCh38#207888871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64879343-C-A

207889359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64880088-T-C

207889408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64880138-T-A

207891578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64881894-G-C

http://identifiers.org/hco/2/GRCh38#207892080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64882498-C-A

207892686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64883081-C-T

207892748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64883144-C-G

http://identifiers.org/hco/2/GRCh38#207894385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64884297-C-A

207894471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64884367-G-A

207894538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64884429-T-C

207895041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64884914-G-C

207895247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64885117-C-G

http://identifiers.org/hco/2/GRCh38#207895625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64885441-C-A

207896097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64886343-T-C

207896102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64886349-G-A

207896520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64886722-T-C

207896600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64886801-T-C

207896604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64886805-T-C

207896658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64886859-A-G

207896966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64887155-T-C

207896967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64887156-G-T

207897014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64887268-C-G

207897270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64887520-T-C

207897741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64888060-G-A

207898039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64888356-G-T

207898387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64888697-A-G

207899150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64889335-T-G

207899242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64889417-T-A

http://identifiers.org/hco/2/GRCh38#207899279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64889453-C-A

207899800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64889900-C-G

207899851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64889950-A-G

207899962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64890055-G-A

207900098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64890143-T-C

207900209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64890242-G-A

207900209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64890242-G-T

207900525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64890528-G-A

http://identifiers.org/hco/2/GRCh38#207900970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64891940-C-A

207900970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64891940-C-G

207900975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64891945-G-A

207900975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64891945-G-T

207901012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64891990-G-A

207901012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64891990-G-T

207901181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64892141-T-C

207901270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 64892234-T-C

207901296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 64892260-T-A

207901296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 64892260-T-C

207901298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, missense_variant
orthologous variants: 64892262-G-C

http://identifiers.org/hco/2/GRCh38#207901387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64892353-C-A

207901393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64892359-G-A

http://identifiers.org/hco/2/GRCh38#207901412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64892380-C-A

207901459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64892454-G-A

http://identifiers.org/hco/2/GRCh38#207901703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64892705-C-A

http://identifiers.org/hco/2/GRCh38#207901785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64892788-C-A

207901785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64892788-C-T

http://identifiers.org/hco/2/GRCh38#207901810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64892813-C-A

207902552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64893586-G-A

207902569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64893653-C-G

http://identifiers.org/hco/2/GRCh38#207902602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64893712-A-C

207902602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64893712-A-G

207902831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64894010-T-A

207902831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64894010-T-C

207902863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64894040-T-C

207903236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64894500-C-T

207903329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64894629-A-T

207903330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64894630-G-A

207903330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64894630-G-C

207903341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64894637-G-A

207903349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64894645-G-A

207903349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64894645-G-C

207903465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64894763-G-T

207903678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64894948-T-C

207903745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64895011-G-A

207903768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64895035-G-C

207903768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64895035-G-T

207903877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64895130-T-A

207904389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64896591-C-T

207904391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64896593-C-T

207904421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64896625-T-G

http://identifiers.org/hco/2/GRCh38#207904790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64896858-C-A

207905199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64897384-C-T

207905267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64897453-T-A

207905681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64897933-T-C

207905734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64897984-T-C

207905962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64898211-C-T

207906012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64898254-C-T

207906711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64898725-C-T

http://identifiers.org/hco/2/GRCh38#207907085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64899182-A-C

207907189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64899289-T-G

207907624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64899403-A-G

207907832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64899595-G-A

207908057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64899812-T-C

207908517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 64900349-C-T

207908550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 64900382-T-C

http://identifiers.org/hco/2/GRCh38#207908675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64900499-C-A

207908675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64900499-C-T

207908707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64900527-G-T

207908772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64900586-G-A

http://identifiers.org/hco/2/GRCh38#207909012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64901303-A-C

207909307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64901605-G-A

207909624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64902176-T-C

207909710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64902253-T-A

207909774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64902302-A-T

207909879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64902406-T-C

207910322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64902821-G-C

207910444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64902954-C-T

207910514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64903040-G-A

207910807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64903774-G-A

207910954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64903921-G-A

207910954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64903921-G-C

207911073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64904033-G-C

207911132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64904077-A-G

207911404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64904299-C-T

207911850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64904805-G-T

207912643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64905570-A-G

http://identifiers.org/hco/2/GRCh38#207914917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64908004-C-A

207915011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64908108-G-T

207915050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64908134-G-A

207915050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64908134-G-C

207915088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64908172-T-C

207915088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64908172-T-G

207915116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64908200-G-C

207915254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64908291-C-G

http://identifiers.org/hco/2/GRCh38#207915320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64908353-A-C

http://identifiers.org/hco/2/GRCh38#207915322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64908355-A-C

207915530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64908572-A-G

207915536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64908613-C-G

207915799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64912077-C-T

207916008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64912270-A-T

207916035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64912297-T-C

207916078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64912340-G-A

207916314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64912576-G-A

http://identifiers.org/hco/2/GRCh38#207917387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64913333-C-A

http://identifiers.org/hco/2/GRCh38#207918940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64914649-C-A

http://identifiers.org/hco/2/GRCh38#207918948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64914657-A-C

207918952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64914661-C-T

207918967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64914672-A-T

207919036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64914745-G-A

207919054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64914763-G-A

207919381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64914986-C-T

207919427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915038-T-C

207919490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915085-G-A

207919784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915340-A-G

207919784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915340-A-T

207920041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915456-C-T

207920124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915531-T-A

207920145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915552-G-A

207920358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915732-C-T

207920366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915740-G-C

207920410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915779-G-C

207920411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915780-A-G

207920475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915838-C-T

207920577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915925-G-A

207920603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64915954-T-C

http://identifiers.org/hco/2/GRCh38#207920677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64916023-C-A

207920677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64916023-C-T

207920764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64916109-T-C

207920764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64916109-T-G

207920815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64916160-G-A

207920827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64916172-C-G

207922951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64917013-A-G

207922998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64917047-G-A

207923169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64917168-G-A

207923272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64917251-T-C

207923279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64917258-C-T

207926665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64918054-T-C

207926815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64918203-G-A

207928464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64919803-C-G

207928507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64919842-G-A

207928737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64920076-G-T

207928743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64920082-T-C

207928922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64920354-T-C

207929569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64920989-A-G

207929621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64921261-C-T

207929726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64921346-T-C

http://identifiers.org/hco/2/GRCh38#207930012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64921648-A-C

207930074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64921711-G-T

207930191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64921831-G-A

207930645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64922096-G-C

207930798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64922199-G-C

207930798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64922199-G-T

207930928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 64922290-G-A

207930954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: missense variant
orthologous variants: 64922316-C-G

207931020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: synonymous variant
orthologous variants: 64922382-G-A

207931081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: synonymous variant
orthologous variants: 64922443-G-A

http://identifiers.org/hco/2/GRCh38#207931189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64922555-C-A

207931189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64922555-C-T

207931291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64922651-G-C

207931397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64922764-T-C

207931401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64922768-C-T

207931414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64922787-C-T

207931627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64923031-T-C

207931632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64923036-A-G

207932439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64923198-T-G

207932914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64923658-G-A

207932966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64923710-A-G

207933657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64924438-G-A

207934223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64925064-A-G

http://identifiers.org/hco/2/GRCh38#207934256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64925089-C-A

207934683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64925554-G-A

http://identifiers.org/hco/2/GRCh38#207934937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64925808-C-A

207935111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64925968-T-C

207935290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64926241-C-T

207935332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64926336-T-C

207935388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, undefined
orthologous variants: 64926389-G-A

207935418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64926418-C-T

207935485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64926469-C-G

207935552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64926520-G-A

207935733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64926691-A-G

207935733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64926691-A-T

207938302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64927386-C-G

207938559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64927632-G-C

207938559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64927632-G-T

207938973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64928014-C-T

207939078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64928093-G-A

207939201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64928186-G-A

207939317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64928299-G-A

207939449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64928439-T-C

207939598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64928569-C-T

207939787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64928723-G-C

207939866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64928804-T-A

207939866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64928804-T-C

207939866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64928804-T-G

207939869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64928807-C-T

207940103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64929058-A-G

207944360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64929965-T-G

207944427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64930032-T-C

207944530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64930107-C-T

207944599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64930167-T-C

http://identifiers.org/hco/2/GRCh38#207944612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64930180-A-C

207944612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64930180-A-G

207945198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64930727-C-T

207945617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64931152-T-C

207945791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64931392-C-G

207945872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64931462-G-C

207945876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64931466-G-C

207945912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64931515-G-A

207945912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64931515-G-C

207945915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64931518-G-A

207946400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: synonymous variant
orthologous variants: 64931944-G-A

207946430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: synonymous variant
orthologous variants: 64931974-G-A

207946430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: missense variant
orthologous variants: 64931974-G-C

207946460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: synonymous variant
orthologous variants: 64932004-G-A

207946542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64932084-T-C

207946559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64932099-A-G

207946622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64932117-G-A

207946712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64932198-G-T

207947059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64932982-G-A

207947374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64933303-C-T

207947512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64933419-G-A

207948006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64933874-A-G

207948147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64934085-T-C

207948167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64934098-T-C

207949006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64934283-T-A

207950602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64935804-G-A

http://identifiers.org/hco/2/GRCh38#207951047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64936254-A-C

207951107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64936312-A-G

207951806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64936995-T-C

207952023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64937188-C-T

207952125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64937299-A-G

207952298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64937735-C-T

207952646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64938352-T-C

207953138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64938803-G-A

207953333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64942519-G-A

207953454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64942641-T-C

207954491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64943018-G-C

207954561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64943087-T-C

http://identifiers.org/hco/2/GRCh38#207954617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64943143-C-A

207954665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64943185-A-G

207954761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64943309-C-T

207954798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64943342-C-T

207955000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64943785-T-C

207955159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64943946-T-C

207955170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64943957-G-A

207958011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64944592-T-C

207958189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64944747-C-T

207958205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64944764-A-G

http://identifiers.org/hco/2/GRCh38#207958242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64944814-A-C

207958242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64944814-A-G

207958302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64944862-C-T

207959217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64945318-C-T

207960024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64946076-C-T

207960442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64946568-G-A

207961382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64947454-T-C

207961595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64947646-A-T

207961634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64947683-G-A

207961861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64947866-C-T

207961911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64947914-T-G

207961918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64947921-C-T

207961927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64947930-C-G

207961946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64947949-G-T

207962078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64948070-C-T

207962201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64948179-G-C

207962332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64948323-A-G

207962366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64948355-G-A

207962377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64948366-C-T

207962494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64948444-A-G

207962552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64948488-T-G

207962806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64948692-T-C

http://identifiers.org/hco/2/GRCh38#207962910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64948786-C-A

207962910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64948786-C-T

207963413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64949492-A-G

207963484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64949566-G-C

207963893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64949939-C-T

http://identifiers.org/hco/2/GRCh38#207964203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64950079-C-A

207964307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64950197-G-T

207964753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64950618-C-T

207965042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64951009-T-C

207965140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64951104-A-G

207965155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64951119-C-G

207965167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64951130-A-G

207965204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64951167-G-A

207965250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64951213-G-A

207965261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64951224-C-G

207965930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64951871-T-G

207966365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64952437-A-G

207966813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64952742-A-G

207966833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64952761-G-T

207966850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64952776-C-T

207966851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64952777-A-G

207966885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64952809-A-G

207967564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64953307-A-G

207967564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64953307-A-T

207967713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64953370-C-T

207968061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64953682-T-A

207968210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64953806-T-C

207968258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64953862-C-G

http://identifiers.org/hco/2/GRCh38#207968913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64954496-C-A

207969140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64954717-C-T

207969189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64954766-A-G

http://identifiers.org/hco/2/GRCh38#207969260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64954821-C-A

207969353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64954902-A-G

207969445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64954998-G-A

207969469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64955022-T-C

207969753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64955309-C-T

207970171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64955676-T-C

207970532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64956061-A-G

207970867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64956389-A-G

207970953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64956474-T-C

207971009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64956520-T-G

207971140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64956641-T-C

207972251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64957448-A-G

http://identifiers.org/hco/2/GRCh38#207972332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64957466-C-A

207972333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64957467-A-G

207972333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64957467-A-T

207972519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64957498-G-A

207972558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64957500-G-A

207972923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64957809-C-G

207973316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64958156-A-T

207974204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64958672-C-T

207974316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64958763-C-G

207974710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64959148-T-C

207975284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64959554-A-G

207975305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64959575-C-T

207975591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64959834-T-A

207976697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 64960755-A-G

207976954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, missense_variant
orthologous variants: 64961012-T-C

http://identifiers.org/hco/2/GRCh38#207976970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64961028-C-A

207976994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 64961052-T-C

207977003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 64961061-G-A

207977552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 64961607-C-G

207977688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64961722-G-T

207977690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64961724-A-G

207978277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64961942-T-C

207978413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64961996-G-C

207978530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64962102-C-T

207978586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64962157-C-G

207978677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64962243-A-T

207978682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64962248-G-A

207978754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64962318-C-T

207978919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64962474-G-C

http://identifiers.org/hco/2/GRCh38#207979123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64962836-C-A

207979674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64963371-T-C

http://identifiers.org/hco/2/GRCh38#207979801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64963504-C-A

207979989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64963693-G-T

207980340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64963984-G-C

http://identifiers.org/hco/2/GRCh38#207981096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64964114-A-C

http://identifiers.org/hco/2/GRCh38#207981209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64964206-C-A

http://identifiers.org/hco/2/GRCh38#207981336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64964330-C-A

http://identifiers.org/hco/2/GRCh38#207983655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64964978-C-A

207983655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64964978-C-G

207989037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64966273-A-G

207989151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64966388-T-C

207989258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64966481-G-A

http://identifiers.org/hco/2/GRCh38#207989514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64966725-C-A

207989514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64966725-C-T

207989923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64967203-T-C

207990098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64967370-C-G

207990386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64967641-G-A

207990510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64967761-T-C

207990770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64968596-C-T

207990849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64968672-T-C

207990865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64968687-T-G

207991030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64968797-G-A

207991030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64968797-G-C

207991300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64968989-C-T

207991530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64969207-T-A

207991853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64969453-T-A

207991879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64969480-C-G

207991908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64969508-A-G

http://identifiers.org/hco/2/GRCh38#207992578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64971345-A-C

http://identifiers.org/hco/2/GRCh38#207992703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64971469-C-A

207992816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64971577-G-A

207992920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64971685-G-C

207992920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64971685-G-T

207993023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64972005-T-C

207993122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64972100-A-G

207993130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64972111-T-C

207993323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64972298-C-T

207993442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64972416-G-C

207993529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64972507-G-A

207994084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64973047-G-A

207994215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64973283-A-G

207994344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64973421-G-A

207994652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64974090-C-T

207998150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 64974993-G-A

207998353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 64975149-C-G

207998882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 64975522-T-C

208000399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64976325-T-A

208000642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64976544-C-T

208000769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64976686-C-T

208001098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: missense variant
orthologous variants: 64976924-G-A

208001098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: missense variant
orthologous variants: 64976924-G-C

208001098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: missense variant
orthologous variants: 64976924-G-T

208001256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: synonymous variant
orthologous variants: 64977085-G-A

208001344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: missense variant
orthologous variants: 64977173-C-T

http://identifiers.org/hco/2/GRCh38#208001499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64977328-C-A

208001520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: synonymous variant
orthologous variants: 64977349-C-T

208001528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: missense variant
orthologous variants: 64977357-C-G

http://identifiers.org/hco/2/GRCh38#208001529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#64977358-A-C

http://identifiers.org/hco/2/GRCh38#208001571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64977400-C-A

208001571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: synonymous variant
orthologous variants: 64977400-C-T

208001586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: synonymous variant
orthologous variants: 64977415-T-C

208001607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: synonymous variant
orthologous variants: 64977436-T-C

208001992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64977733-G-A

208001992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64977733-G-T

http://identifiers.org/hco/2/GRCh38#208002009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64977750-A-C

208002009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64977750-A-G

208002011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64977752-T-C

http://identifiers.org/hco/2/GRCh38#208002098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64977842-C-A

208002098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64977842-C-T

208002239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64977985-C-T

http://identifiers.org/hco/2/GRCh38#208002368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64978107-A-C

208002383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64978122-G-C

208002486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64978215-G-C

208002526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64978259-C-T

208002581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64978317-C-G

208002695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64978466-G-A

208003438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64978831-T-C

208003467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64978860-T-C

208003584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64979192-G-C

208003909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64979450-T-C

208005791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64979981-T-C

http://identifiers.org/hco/2/GRCh38#208005830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64980101-C-A

208005830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64980101-C-T

208007185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64981474-C-T

208007191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64981480-G-A

208007328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64981625-G-A

http://identifiers.org/hco/2/GRCh38#208007347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64981641-C-A

208007378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64981670-C-T

http://identifiers.org/hco/2/GRCh38#208008527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64983141-A-C

208010898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64984459-G-C

208010899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64984460-A-G

208014415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64985800-G-A

208015321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64986754-A-T

208015415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64986845-C-T

208015896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64987294-A-G

208020358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64990548-C-G

208020392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64990591-T-C

208020411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64990778-G-T

208020589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 64990950-C-T

208020604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 64990965-G-A

208020812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64991156-G-C

208020837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64991181-T-C

208021109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64991442-G-A

208021109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64991442-G-C

208021298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64991650-C-G

208021298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64991650-C-T

208021542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64992266-C-G

208021542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64992266-C-T

208021811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64992499-G-C

208022826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64993805-T-C

208022891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64993878-C-G

208023141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64994113-C-T

http://identifiers.org/hco/2/GRCh38#208024151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64994655-A-C

208024347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64994820-T-C

208024397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64994870-T-G

http://identifiers.org/hco/2/GRCh38#208024536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64994999-A-C

208024817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64995256-C-T

208025190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64995603-A-G

208025254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64995665-T-C

208025353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64995744-G-A

208025353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: intron variant
orthologous variants: 64995744-G-T

208025441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 5 prime UTR variant
orthologous variants: 64995817-T-C

http://identifiers.org/hco/2/GRCh38#208025454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#64995831-C-A

208025511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34006
most severe consequence: 5 prime UTR variant
orthologous variants: 64995888-G-T