http://identifiers.org/hco/7/GRCh38#16791884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36055067-C-A

16791884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36055067-C-T

16791888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36055063-A-G

http://identifiers.org/hco/7/GRCh38#16791894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36055061-C-A

16791895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36055060-A-G

16791899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36055056-G-A

16791899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36055056-G-T

16791913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36055052-G-T

16791946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36055021-A-G

http://identifiers.org/hco/7/GRCh38#16792037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36054944-C-A

16792079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36054907-G-A

16792079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36054907-G-T

16792124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36054869-A-G

16792505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36054428-T-C

16792541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36054386-T-C

16792596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36054338-G-A

16792596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3 prime UTR variant
orthologous variants: 36054338-G-T

16792980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36053827-G-T

16793007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36053800-C-T

16793008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36053799-G-A

16793008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36053799-G-T

16793421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36053324-G-A

16793946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36052687-T-C

16793957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36052676-C-T

16793994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36052640-G-A

http://identifiers.org/hco/7/GRCh38#16794008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36052630-A-C

http://identifiers.org/hco/7/GRCh38#16794052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36052582-A-C

16794179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36052496-C-T

16794191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36052484-A-G

16794196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36052479-G-A

16794264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36052438-G-T

16794552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, undefined
orthologous variants: 36052159-T-C

16794553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, undefined
orthologous variants: 36052158-G-A

16794553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, undefined
orthologous variants: 36052158-G-T

16794605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, undefined
orthologous variants: 36052084-A-T

16794617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, undefined
orthologous variants: 36052073-C-G

16794646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, undefined
orthologous variants: 36052043-G-A

http://identifiers.org/hco/7/GRCh38#16794656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#36052034-C-A

16794656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, undefined
orthologous variants: 36052034-C-G

16794656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, undefined
orthologous variants: 36052034-C-T

16794682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36052007-G-C

16794682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36052007-G-T

http://identifiers.org/hco/7/GRCh38#16794693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#36051997-C-A

16794693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36051997-C-G

16794693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36051997-C-T

http://identifiers.org/hco/7/GRCh38#16794697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#36051993-C-A

16794726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36051964-T-G

16794727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36051963-T-G

16794729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36051961-A-G

16794729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36051961-A-T

http://identifiers.org/hco/7/GRCh38#16794755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36051932-A-C

16794755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 36051932-A-T

16794771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36051921-G-A

16794771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36051921-G-T

16794786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36051906-G-A

16794786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 36051906-G-T

http://identifiers.org/hco/7/GRCh38#16794809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36051883-C-A

16794860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, missense_variant
orthologous variants: 36051833-C-T

16794937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 36051765-C-T

16795027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 36051675-G-C

16795027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 36051675-G-T

16795092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36051623-A-G

16795102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36051613-C-T

16795135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36051583-G-A

16795135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36051583-G-T

16795162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36051559-T-C

16795181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36051539-C-T

http://identifiers.org/hco/7/GRCh38#16795359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36051348-C-A

16795359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36051348-C-T

16795414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36051289-C-G

16795670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36050361-A-G

http://identifiers.org/hco/7/GRCh38#16795810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36049807-C-A

16795810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36049807-C-G

16795834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36049786-C-T

16795925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36049703-C-T

16796060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36049596-C-G

16796060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36049596-C-T

16796136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36049520-T-A

16796144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36049512-T-C

16796318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36049353-C-T

16796336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36049336-T-A

16796392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36049309-T-C

16796633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36049062-G-A

16797414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36048898-T-A

16797449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36048865-G-A

16797651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: missense variant
orthologous variants: 36048623-A-G

16799499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36047805-A-G

16799507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36047797-G-A

16799507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36047797-G-T

16799519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36047784-T-A

16799519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36047784-T-G

16799550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36047758-A-G

16799550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36047758-A-T

16799618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36047609-T-C

16799618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36047609-T-G

16799656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36047573-T-A

16799656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36047573-T-G

16799701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36047538-T-C

16800008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36047244-C-T

16800015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36047237-C-G

16800078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36047170-C-T

16800096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36047156-A-T

16800302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36046943-G-A

16800517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36046716-T-C

16800677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36046572-T-C

http://identifiers.org/hco/7/GRCh38#16801009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36046254-C-A

16801009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36046254-C-T

http://identifiers.org/hco/7/GRCh38#16801225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36046046-C-A

16801225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36046046-C-G

16801225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36046046-C-T

16801261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36046014-T-C

16801276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36045999-C-G

16801276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 36045999-C-T

16801296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36045979-G-C

16801303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36045972-G-A

16801344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36045931-T-G

16801353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 36045922-G-A

16801399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36045876-T-A

16801399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36045876-T-C

http://identifiers.org/hco/7/GRCh38#16801483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36045808-A-C

16801525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36045770-A-G

16801909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36045438-G-A

16801909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36045438-G-C

16801909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36045438-G-T

16803148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36044711-A-G

16803206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36044651-A-G

16803221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36044630-G-T

16803232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36044619-T-C

16803380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36044479-C-T

16803668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36044187-C-T

16803674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36044181-A-G

http://identifiers.org/hco/7/GRCh38#16803695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36044152-C-A

16803695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36044152-C-G

16803731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36044116-T-C

http://identifiers.org/hco/7/GRCh38#16803737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36044112-C-A

16803775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36044071-C-T

16803957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043895-G-C

16803958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043894-G-A

16803958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043894-G-T

16804060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043800-G-C

16804088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043772-G-C

16804111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043750-G-A

16804377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043470-T-G

16804496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043391-A-G

16804620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043269-G-T

16804731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043155-C-T

16804807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043081-A-G

http://identifiers.org/hco/7/GRCh38#16804822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36043067-C-A

16804822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043067-C-G

16804823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043066-T-C

16804823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043066-T-G

16804833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043056-T-C

16804834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043055-G-T

16804855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36043033-G-A

http://identifiers.org/hco/7/GRCh38#16804893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36043000-C-A

16804954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36042948-T-C

16805035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36042869-G-A

16805096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36042808-T-A

16805154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36042734-A-G

16805429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36042433-T-C

16805460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36042402-A-G

http://identifiers.org/hco/7/GRCh38#16805532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36042350-C-A

16805555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36042327-G-A

16805559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36042323-G-A

16805559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36042323-G-T

16807223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36040046-G-C

16807250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36040026-A-G

16808041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36039368-G-A

16808121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36039290-G-A

16808144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36039269-G-A

16808303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36039117-G-T

16808339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36039060-C-T

http://identifiers.org/hco/7/GRCh38#16808453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36038928-C-A

16808453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36038928-C-T

16808497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36038886-T-C

16808912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36038494-A-G

16808970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36038433-A-G

16808977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36038426-C-T

16809387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36038039-G-C

http://identifiers.org/hco/7/GRCh38#16809421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36037995-C-A

16809421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36037995-C-G

16809435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36037981-G-C

http://identifiers.org/hco/7/GRCh38#16809471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36037945-A-C

16809593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36037786-G-A

16809719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36037661-G-A

16809757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36037626-A-G

16809893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36037496-C-T

http://identifiers.org/hco/7/GRCh38#16809894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36037495-C-A

16809894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36037495-C-T

16809899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36037493-G-A

16809905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36037487-A-G

16810171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36037040-A-G

16810176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36037035-C-T

16810189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36037022-T-C

http://identifiers.org/hco/7/GRCh38#16810347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36036847-C-A

16810609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36036594-T-C

16810751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36036486-A-G

16810751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36036486-A-T

16810831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36036407-T-C

16810889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36036353-T-C

16811063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36036133-A-G

16811130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36036069-C-G

16811130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36036069-C-T

16811344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36035813-T-C

16811743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 5 prime UTR variant
orthologous variants: 36034965-G-C

http://identifiers.org/hco/7/GRCh38#16812844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36034234-A-C

16812921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36034152-T-C

16812986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36034084-A-G

16813058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36034012-A-G

16813254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033816-T-A

16813476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033602-G-T

16813531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033547-A-G

16813540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033538-G-A

16813669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033440-G-A

16813669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033440-G-T

16813681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033428-G-A

16813781-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033346-G-C

16813781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033346-G-T

16814027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033310-G-A

16814027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033310-G-T

16814042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033307-T-C

16814246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36033155-T-C

http://identifiers.org/hco/7/GRCh38#16814401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36033019-C-A

16814474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36032947-A-G

16815355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36031726-C-G

16815585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36031504-A-G

16822122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36029834-A-T

16822206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36029750-T-A

16822553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36029410-G-A

16822659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36029291-G-C

http://identifiers.org/hco/7/GRCh38#16823037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36029018-A-C

16823151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36028825-A-G

16823222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36028682-T-A

16823614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36028290-C-T

16824011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36027989-C-G

16824184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36027820-T-C

16824447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36027574-A-G

16824567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36027481-A-G

16824753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36027293-T-A

16824872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36027201-C-G

16824872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36027201-C-T

16825232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36026858-A-G

16825285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36026798-T-C

16825304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36026777-C-T

http://identifiers.org/hco/7/GRCh38#16833107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36026666-C-A

http://identifiers.org/hco/7/GRCh38#16833153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#36026612-C-A

16833153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36026612-C-T

16833222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: intron variant
orthologous variants: 36026541-A-G

16833308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 5 prime UTR variant
orthologous variants: 36026449-T-C

16833378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 5 prime UTR variant
orthologous variants: 36026390-T-C

16833403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 328
most severe consequence: 5 prime UTR variant
orthologous variants: 36026358-A-G