95077155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980766-A-G

95077243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980688-G-A

95077257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980666-A-G

95077323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980594-G-A

95077380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980549-G-T

95077431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980502-G-T

95077446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980487-A-G

95077618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980381-T-C

95077623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980376-A-G

95077639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980357-G-A

95077639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980357-G-T

95077695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980290-A-G

95077857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980091-C-T

95077925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93980069-A-G

95078163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979898-G-T

95078169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979892-G-A

95078169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979892-G-T

95078189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979872-A-G

95078245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979829-G-A

95078338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979767-G-T

95078351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979754-G-A

95078352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979753-C-T

http://identifiers.org/hco/12/GRCh38#95079609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93979457-C-A

95079609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979457-C-G

95079667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979405-T-C

95079729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979342-A-G

http://identifiers.org/hco/12/GRCh38#95079795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93979285-A-C

95079795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979285-A-G

95079851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979199-G-A

95079851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979199-G-T

95080279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93979109-G-A

http://identifiers.org/hco/12/GRCh38#95080396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93979003-C-A

http://identifiers.org/hco/12/GRCh38#95080412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93978987-C-A

95080590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93978682-C-T

95080640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93978634-G-T

95080737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93978536-G-A

95081049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93978107-G-T

95081176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93977987-T-C

95081222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93977940-A-T

95081301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93977864-G-T

95081385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: 93977784-A-G

http://identifiers.org/hco/12/GRCh38#95081392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93977777-C-A

http://identifiers.org/hco/12/GRCh38#95081400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93977769-A-C

95081400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 93977769-A-G

95081400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 93977769-A-T

95081460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 93977709-T-C

95081467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 93977702-T-C

http://identifiers.org/hco/12/GRCh38#95081980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93977557-C-A

95082012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93977526-A-G

95082042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93977492-C-T

95082157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93977175-T-C

95082212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93977116-C-G

95082212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93977116-C-T

95082291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93977037-T-C

95082684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93976952-A-G

95083945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93976165-G-T

95084183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93975978-G-T

95084378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93975854-A-G

95084404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93975828-G-A

95084404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93975828-G-T

95084427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93975805-G-T

95084462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93975779-T-C

95084465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93975776-T-C

95084465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93975776-T-G

95084516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93975729-T-C

http://identifiers.org/hco/12/GRCh38#95084528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93975717-A-C

95084531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93975714-A-G

http://identifiers.org/hco/12/GRCh38#95084612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93975633-C-A

95084612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93975633-C-T

95084614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 93975631-T-C

95084662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93975583-A-G

95084669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93975575-G-A

95084683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93975561-G-T

95085576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 93974829-A-G

95085590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 93974817-T-C

95085602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 93974805-T-A

95085608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 93974799-G-T

95085874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 93974178-C-G

95085930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93974121-A-G

95085932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93974119-G-C

95085955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93974096-A-G

95085971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93974070-T-C

http://identifiers.org/hco/12/GRCh38#95089337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93973617-A-C

http://identifiers.org/hco/12/GRCh38#95089483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93973474-C-A

95089483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93973474-C-T

95089892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93973134-C-G

95090486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93972373-T-A

95091172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93971763-G-A

95091426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93971312-C-T

95091523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93971200-C-G

95091630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93971050-G-T

95091820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93970866-A-G

http://identifiers.org/hco/12/GRCh38#95091851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93970843-A-C

95091851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93970843-A-G

95091854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93970840-T-A

95091887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93970807-T-G

95091913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93970780-G-A

95091913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93970780-G-T

95091939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93970756-G-A

95091939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93970756-G-T

95092123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93970609-T-A

http://identifiers.org/hco/12/GRCh38#95092151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93970563-A-C

95092670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93970032-C-T

95092679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93970023-T-C

95092851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 93969855-G-A

http://identifiers.org/hco/12/GRCh38#95092881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93969827-C-A

http://identifiers.org/hco/12/GRCh38#95092889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93969819-C-A

95092889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93969819-C-T

http://identifiers.org/hco/12/GRCh38#95094482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93969363-C-A

http://identifiers.org/hco/12/GRCh38#95094524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93969321-C-A

95094524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93969321-C-G

95094524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93969321-C-T

95094555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93969285-A-T

95094574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93969260-A-G

95094581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93969253-G-A

95094581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93969253-G-T

95094583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93969251-A-G

95094593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 93969241-T-A

95094593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: 93969241-T-C

95094600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 93969234-G-A

95094600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 93969234-G-T

95094740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93969093-C-T

95096232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93966515-C-T

95096324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93966350-C-T

95096334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93966340-A-G

95096473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93966213-C-T

http://identifiers.org/hco/12/GRCh38#95096475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93966211-C-A

95096783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93965925-T-C

95096791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93965917-G-T

95096836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93965877-T-A

95096883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93965830-A-G

http://identifiers.org/hco/12/GRCh38#95105103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93963212-C-A

95105103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93963212-C-T

http://identifiers.org/hco/12/GRCh38#95105230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93963082-C-A

95105230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93963082-C-T

95105453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93962809-A-G

http://identifiers.org/hco/12/GRCh38#95105570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93961763-C-A

95105570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93961763-C-T

95105713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93961627-A-G

95105713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93961627-A-T

95107051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93961395-C-T

95107107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93961342-A-G

95107296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93961077-A-G

95107410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93960950-T-C

95107440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93960927-G-A

95107440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93960927-G-T

95107466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93960902-T-C

95107474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93960894-G-A

95107474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93960894-G-T

95107531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93960843-C-G

95107531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93960843-C-T

95107676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93960705-A-G

http://identifiers.org/hco/12/GRCh38#95107700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93960676-C-A

95107709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93960667-T-C

95107765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93960622-T-C

95107820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93960565-A-G

95107840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93959933-T-C

95107925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93959854-G-A

95107925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93959854-G-T

95108051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93959746-C-T

95108114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93959675-T-A

http://identifiers.org/hco/12/GRCh38#95108294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93959526-A-C

95108295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93959525-T-C

95108295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93959525-T-G

95108352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 93959471-C-G

95108455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93959274-G-A

95108456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93959273-G-A

95108472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93959242-C-T

95108698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93958966-G-A

95108698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93958966-G-T

95108749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93958882-C-G

95110289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93958869-C-T

95110290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93958868-A-G

95111565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93958186-C-T

95111763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93957998-A-G

95113578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93956429-A-G

95113615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93956396-A-T

95113670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 93956344-T-C

95113717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93956297-A-G

95113743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93956275-G-A

95115873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93954483-T-C

95115947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93954414-C-T

95116051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93954295-A-G

95116211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93954000-C-G

95116211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93954000-C-T

95116246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93953918-G-C

95116317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93953604-A-G

95116323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93953598-T-C

95116890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 93952899-G-A

95116905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, start_lost, undefined
orthologous variants: 93952883-C-T

95116914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93952874-G-A

http://identifiers.org/hco/12/GRCh38#95117289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93952340-C-A

95117359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93952276-G-A

95117359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93952276-G-C

95118592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93951991-T-A

95123458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93948701-A-G

95124271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93948526-T-C

95124385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93948411-C-T

95124455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93948337-G-T

95124506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93948289-T-G

http://identifiers.org/hco/12/GRCh38#95124572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93948223-C-A

95124645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93948154-G-T

95126999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93947373-A-G

95127008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93947364-T-A

95127136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93947264-A-T

95127609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93946935-A-G

95127610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93946934-T-C

95127621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93946923-T-C

95127622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93946922-A-T

http://identifiers.org/hco/12/GRCh38#95127683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93946861-C-A

95127713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93946832-T-C

95127779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93946763-T-C

95127820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93946721-C-G

95127846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93946698-T-G

95127880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93946662-G-C

95127884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93946658-T-A

95128071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93946471-A-G

http://identifiers.org/hco/12/GRCh38#95128711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93946298-A-C

95128883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93946095-T-C

95128937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93945982-A-G

95129073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93945838-T-C

95129081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93945822-G-T

95129101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93945804-T-C

95129106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93945799-T-C

95129108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93945797-G-A

95129329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93945646-A-G

95130033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93945266-A-G

95130036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93945263-C-T

95130085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93945213-A-G

95130228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93944992-T-C

95130238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93944981-C-G

95130238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93944981-C-T

95130284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93944943-T-C

95130505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93944738-G-A

95130521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93944722-G-A

95130521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93944722-G-T

http://identifiers.org/hco/12/GRCh38#95130607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93944632-A-C

95130607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93944632-A-G

95131906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93944299-G-A

http://identifiers.org/hco/12/GRCh38#95132008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93944206-A-C

95132018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93944196-T-A

http://identifiers.org/hco/12/GRCh38#95132029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93944184-A-C

95132047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93944166-A-G

http://identifiers.org/hco/12/GRCh38#95133478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93942906-A-C

95133604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93942780-C-T

95133672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93942708-T-C

95134100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93942352-C-T

95134580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93942045-G-A

95134633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93942027-G-A

95134633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93942027-G-T

95134636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93942024-G-A

95134730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93941941-G-A

95134871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93941795-G-A

95134871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93941795-G-C

95134876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93941790-G-A

95134876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93941790-G-C

95135104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93941629-C-T

95135127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93941612-G-C

95135269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93941481-T-C

95135328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93941423-A-T

http://identifiers.org/hco/12/GRCh38#95135507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93941171-C-A

95135580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93941108-A-G

95135671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93941032-C-T

95136053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93940799-T-C

95136056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93940796-T-C

95136135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93940749-G-A

95136479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93940562-G-A

95136825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93940254-C-T

http://identifiers.org/hco/12/GRCh38#95136963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93940136-C-A

95136963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93940136-C-T

95137352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93939629-T-C

95137425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93939526-T-C

95137429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93939522-T-C

http://identifiers.org/hco/12/GRCh38#95137432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93939353-C-A

95137432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93939353-C-T

95137507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93939273-G-C

95137507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93939273-G-T

95137691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93939089-A-G

http://identifiers.org/hco/12/GRCh38#95141287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93936514-A-C

95141304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93936497-A-T

95141314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93936486-G-C

95141314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93936486-G-T

95141331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93936469-T-C

95141344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93936456-A-G

95141351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93936449-G-T

95141354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93936446-A-G

95141578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93936223-T-C

95141578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93936223-T-G

http://identifiers.org/hco/12/GRCh38#95141640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93936161-C-A

95141640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93936161-C-G

95141640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93936161-C-T

95143067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93933051-G-T

95143755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93932049-A-G

95143778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93932017-T-C

http://identifiers.org/hco/12/GRCh38#95143970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93931864-A-C

95144065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931788-C-T

95144105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931750-T-C

95144229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931629-G-C

95144232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931626-T-A

95144232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931626-T-C

95144254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931604-G-A

95144254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931604-G-T

95144282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931576-A-G

95144293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931566-G-A

95145407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931233-C-T

95145408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931232-C-T

95145464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931173-A-G

95145694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93931017-T-C

95145702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93930999-G-C

95146269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93930505-A-T

95146334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93930420-C-G

95146357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93930397-T-C

95146445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93930299-A-G

95146745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93929932-T-C

95146850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93929837-C-G

http://identifiers.org/hco/12/GRCh38#95146893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93929793-A-C

95146910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93929776-C-G

95146910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93929776-C-T

95146949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93929737-G-A

95147070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93929617-A-G

95147320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93929263-T-C

95147441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93929165-A-T

95147995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93928687-A-G

95148134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93928562-G-A

95148249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93928459-G-A

95151942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93926239-T-C

95152749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93925686-G-A

95152749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93925686-G-C

95152749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93925686-G-T

95152888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93925542-G-A

95153005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93925424-A-G

95153039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93925392-A-T

http://identifiers.org/hco/12/GRCh38#95153054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93925377-C-A

95153054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93925377-C-T

95153056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93925375-A-G

95153105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93925338-A-G

http://identifiers.org/hco/12/GRCh38#95153130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93924693-A-C

95153130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93924693-A-G

95154422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93923963-T-C

95154565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93923841-A-G

95154808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93923356-A-G

95155152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93922978-A-G

95159224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93920618-G-A

95162967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-G

95162981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-G

95163248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93918096-G-A

http://identifiers.org/hco/12/GRCh38#95163341-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93917997-A-C

95163480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93917877-G-C

95163914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93917085-A-G

95163959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93917041-C-T

http://identifiers.org/hco/12/GRCh38#95164048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93916946-C-A

95164084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93916913-T-C

95168284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93914538-C-G

95168712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93914426-T-C

95168712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93914426-T-G

95168970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93914169-A-G

95169011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93914123-A-G

95169020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93914114-G-A

95169037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93914088-G-C

95169498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93913641-G-A

95169571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93913571-T-C

95169616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93913537-T-C

95169814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93913377-T-C

95171362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93912186-G-A

95171468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93912069-A-G

95172495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93910312-A-T

http://identifiers.org/hco/12/GRCh38#95172524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93910286-C-A

http://identifiers.org/hco/12/GRCh38#95172720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93910067-C-A

95172724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 93910063-T-C

95172819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93909976-A-G

http://identifiers.org/hco/12/GRCh38#95172821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93909974-C-A

95172821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93909974-C-G

http://identifiers.org/hco/12/GRCh38#95172857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93909939-A-C

95172857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93909939-A-G

http://identifiers.org/hco/12/GRCh38#95172959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93909806-A-C

95173034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93909731-C-T

http://identifiers.org/hco/12/GRCh38#95173322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93909334-C-A

95173686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93908952-T-A

95173700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93908839-A-G

95173800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93908738-C-T

95181248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93904834-G-A

95181645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93904436-T-G

http://identifiers.org/hco/12/GRCh38#95182935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93902881-C-A

95182935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93902881-C-T

95182988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93902825-G-A

95183311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93902563-T-C

95183859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93902335-A-G

95183893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93902303-G-A

95183920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93902275-G-A

95183927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93902268-A-G

95184000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93902195-T-C

95184154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93902043-A-G

95184164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93902034-A-G

95184824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93901574-T-A

95184824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93901574-T-C

95184930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93901503-G-A

http://identifiers.org/hco/12/GRCh38#95185265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93901325-C-A

95185265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93901325-C-T

95185281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93901298-C-T

95185352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93901227-C-T

95185959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93900916-G-A

http://identifiers.org/hco/12/GRCh38#95187728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93898933-C-A

95187728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93898933-C-T

95187756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93898913-C-T

95187994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93898700-G-A

95188021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93898680-C-G

95188758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93898120-A-G

95188892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93898003-C-T

95189171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93897714-A-G

95189196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93897689-G-A

95189241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93897642-A-G

95189893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93897227-T-C

95191532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93896154-C-T

95191618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93896071-G-C

95192350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93895997-G-A

95192366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93895981-T-C

95192483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93895896-T-C

95192550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93895826-G-C

http://identifiers.org/hco/12/GRCh38#95192731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93895665-C-A

http://identifiers.org/hco/12/GRCh38#95197657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93891585-A-C

95197688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93891544-G-A

95197696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93891532-G-A

95197781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93891458-G-A

95197843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93891422-T-C

http://identifiers.org/hco/12/GRCh38#95197899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93891370-A-C

95198166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93891157-A-T

95198216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93891108-T-C

95198216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93891108-T-G

95199090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93890395-A-G

95200454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93889412-T-G

95201035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93888325-A-T

95201117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93888247-G-C

95201184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93888178-T-A

95201266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93888104-T-C

95202752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93886048-T-C

95202924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93885892-T-G

95203185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93885623-T-A

95203315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93885487-A-G

95203600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93885137-C-T

95203608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93885124-G-C

95203697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93885044-G-A

95203697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93885044-G-C

95204105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93884300-C-T

http://identifiers.org/hco/12/GRCh38#95204253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93884167-C-A

95204336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93884091-T-A

95204654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93883821-C-T

http://identifiers.org/hco/12/GRCh38#95205572-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93883197-A-C

http://identifiers.org/hco/12/GRCh38#95207744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

95207744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

95207765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

95207776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

95208396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93881923-A-G

95208423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93881899-G-A

95208480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93881840-C-G

95208713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93881636-G-T

95208719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93881630-T-A

95208719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93881630-T-C

95208719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93881630-T-G

http://identifiers.org/hco/12/GRCh38#95208722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93881627-C-A

95208722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93881627-C-T

http://identifiers.org/hco/12/GRCh38#95208733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93881612-A-C

95208733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93881612-A-G

95208733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 93881612-A-T

95208757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93881591-T-C

95208763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93881585-C-T

http://identifiers.org/hco/12/GRCh38#95208769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93881579-C-A

95208769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93881579-C-T

95208809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93881535-A-G

95208888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93881448-G-A

95208903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93881433-T-C

95208912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93881424-T-C

95208912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93881424-T-G

95208986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 93881350-A-G

95209099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93881258-G-A

95209099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93881258-G-C

95209100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 93881257-G-A

95209138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93881219-C-T

95209248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93881115-A-T

95209311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93881052-G-T

http://identifiers.org/hco/12/GRCh38#95209320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93881043-C-A

95209320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93881043-C-T

95209538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93880825-G-T

95209656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93880704-T-C

95209664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 93880696-G-A

95209717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93880649-A-G

95209898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 93880483-A-G

http://identifiers.org/hco/12/GRCh38#95210087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#93880321-A-C

95210157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93880251-T-C

95210219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93880189-A-T

95210566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93879857-T-C

95210591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 93879832-G-A

95210594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 93879829-G-A

95210594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 93879829-G-T

95210691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93879732-T-C

95210774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 93879649-A-G

95211072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93879357-G-A

95211075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 93879354-G-A

95211075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 93879354-G-T

95211910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93878731-C-T

95212246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93878379-C-G

95212778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93877544-T-C

95212794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93877528-C-T

95213104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93877244-T-A

95213206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93877133-C-T

95213907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93875921-C-T

95213909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93875919-T-G

95214296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93875003-A-G

95214402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93874903-T-C

95214768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93874205-G-A

95215911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93873464-C-T

95216756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93872552-G-A

95217088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93872266-T-C

95217132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93872260-T-C

http://identifiers.org/hco/12/GRCh38#95217133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93872259-C-A

95217165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93872231-C-T

95217187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 93872209-A-G

95217205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 93872190-G-A

95217278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 93872129-C-G

95217316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 93872091-T-C

95217379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 93872039-T-A

95217379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 93872039-T-C

95217379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 93872039-T-G

http://identifiers.org/hco/12/GRCh38#95217420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#93871997-C-A

95217420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21740
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 93871997-C-T