58231744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96251897-C-T

58231853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96252024-T-A

58231853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96252024-T-C

58231853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96252024-T-G

58231978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96252164-G-A

58232224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96252467-G-A

58232341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96252590-C-T

58233272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96252800-T-G

58233717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96253262-T-A

58233718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96253263-G-C

58233830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96253371-T-A

58233854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96253375-A-G

58234893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 5 prime UTR variant
orthologous variants: 96254342-G-A

58234927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 5 prime UTR variant
orthologous variants: 96254376-A-G

58234988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 5 prime UTR variant
orthologous variants: 96254438-G-T

http://identifiers.org/hco/16/GRCh38#58235016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96254465-C-A

http://identifiers.org/hco/16/GRCh38#58235057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96254506-C-A

http://identifiers.org/hco/16/GRCh38#58235161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96254635-C-A

58235161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96254635-C-T

http://identifiers.org/hco/16/GRCh38#58235201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96254712-C-A

http://identifiers.org/hco/16/GRCh38#58235225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96254736-C-A

http://identifiers.org/hco/16/GRCh38#58235250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96254765-C-A

58235540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96255073-T-C

58235687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96255214-T-A

58249773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 96260576-A-G

58249786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96260589-G-T

58249860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96260663-G-A

58249860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96260663-G-C

58249860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96260663-G-T

58249890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96260694-A-G

58249890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96260694-A-T

58249942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 96260747-G-A

http://identifiers.org/hco/16/GRCh38#58249984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96260781-C-A

58249984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 96260781-C-G

58249984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 96260781-C-T

58250137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 96260916-G-A

58250137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 96260916-G-T

58250331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96261116-A-G

58250331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96261116-A-T

58250332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96261117-G-A

58250332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96261117-G-T

58250352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96261137-G-A

58250352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96261137-G-T

http://identifiers.org/hco/16/GRCh38#58250421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96261195-A-C

58250421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96261195-A-G

58251193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96261654-C-T

58251208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96261669-A-G

58251252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96261720-C-G

58251863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96262515-G-A

58252018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96262673-A-G

58252630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96262998-G-T

58252716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 96263080-C-G

58252921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96263293-T-A

58252924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96263296-G-A

58252924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96263296-G-T

http://identifiers.org/hco/16/GRCh38#58252962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96263334-C-A

58252962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96263334-C-T

58253249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96263702-T-C

58253290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96263740-A-G

58253290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96263740-A-T

58253375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96263855-T-A

58253375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96263855-T-C

58253659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96264099-A-G

58253723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96264450-A-G

58253951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96264673-A-G

58253955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96264677-C-G

http://identifiers.org/hco/16/GRCh38#58253972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96264694-A-C

58253972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96264694-A-G

58254045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 96264767-G-T

58254176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96264899-G-A

58254176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96264899-G-C

58254180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96264903-A-G

58254189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96264912-T-G

58254201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96264925-C-T

http://identifiers.org/hco/16/GRCh38#58254205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96264929-C-A

58254205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96264929-C-G

58254205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96264929-C-T

58254257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96265028-T-A

58254270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96265041-G-A

58254270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96265041-G-T

58254320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96265119-T-C

58254530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96265305-A-G

http://identifiers.org/hco/16/GRCh38#58254609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96265390-C-A

58254609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96265390-C-T

58254730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96265545-T-G

58254750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96265564-G-A

58254750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96265564-G-T

58254753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96265567-C-T

58256674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96265785-A-T

58256811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96265897-T-C

58258182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96267266-T-C

58258191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96267275-G-A

58258225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96267295-G-T

http://identifiers.org/hco/16/GRCh38#58258294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96267360-C-A

58258294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96267360-C-T

http://identifiers.org/hco/16/GRCh38#58258316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96267382-A-C

58258316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96267382-A-G

58258421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 96267480-T-A

58259458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96268864-C-T

58259466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96268872-G-A

58259521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96268920-A-G

58259542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96268945-C-T

http://identifiers.org/hco/16/GRCh38#58259768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96269172-C-A

58259768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96269172-C-T

http://identifiers.org/hco/16/GRCh38#58259945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96269341-C-A

58259945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96269341-C-T

58260147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96270346-A-G

58260155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96270354-C-T

58260156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96270355-C-T

58260402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96270588-A-T

58260473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96270660-T-C

58260503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96270690-C-G

58260503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96270690-C-T

58260512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96270699-C-T

58260700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96270911-A-G

58260834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96271038-A-G

58260947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96271122-T-C

58260970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96271133-C-T

58261446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96271408-C-T

58261805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96271804-T-C

58261861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96271962-C-T

58262050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96272244-C-T

58262053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96272247-G-A

58262087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96272277-C-G

58262087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96272277-C-T

58262274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96272425-G-T

58262280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96272431-A-G

58262339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 96272473-A-G

58262461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 96272598-C-T

58262504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 96272641-A-G

http://identifiers.org/hco/16/GRCh38#58262556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96272694-A-C

http://identifiers.org/hco/16/GRCh38#58262571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96272701-C-A

58262571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272701-C-G

58262571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272701-C-T

http://identifiers.org/hco/16/GRCh38#58262589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96272713-A-C

58262597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272721-G-T

58262601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272724-A-G

http://identifiers.org/hco/16/GRCh38#58262622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96272745-C-A

58262622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272745-C-T

58262639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272764-T-C

58262639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272764-T-G

58262656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272791-G-A

58262656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272791-G-C

58262656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272791-G-T

http://identifiers.org/hco/16/GRCh38#58262690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96272839-C-A

58262690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272839-C-G

58262690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272839-C-T

58262749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96272895-T-C

http://identifiers.org/hco/16/GRCh38#58262981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96273042-C-A

58262981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96273042-C-T

58263232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96273286-A-G

58263263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96273318-T-A

58263358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96273689-C-G

58263569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96273906-C-T

58263664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96273937-A-G

58263693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96273949-G-A

http://identifiers.org/hco/16/GRCh38#58264018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96274223-C-A

58264018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96274223-C-T

58264045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96274235-C-T

http://identifiers.org/hco/16/GRCh38#58264442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96274608-C-A

58264442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96274608-C-T

58264510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96274787-A-G

58264873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96275107-T-C

58264960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96275191-C-G

58264976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96275207-G-A

58264976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96275207-G-C

58265092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96275325-C-G

58265092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96275325-C-T

58265128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96275359-G-A

58265133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96275364-T-G

58265147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96275378-G-A

58265161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96275387-C-T

58265184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96275409-G-C

58265347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96275579-G-C

http://identifiers.org/hco/16/GRCh38#58265454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96275685-C-A

58265454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96275685-C-T

58265533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96275754-C-T

http://identifiers.org/hco/16/GRCh38#58265745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96275975-A-C

58265760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron_variant, undefined
orthologous variants: 96275988-T-C

58265871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96276054-G-A

58266007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96276165-C-T

58266361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96276901-G-T

http://identifiers.org/hco/16/GRCh38#58266440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96276924-A-C

58266440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96276924-A-T

58266445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96276929-T-A

58266445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96276929-T-C

http://identifiers.org/hco/16/GRCh38#58266447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96276931-C-A

58266632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277090-G-A

58266834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277262-C-G

58266852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277279-A-G

58266866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277293-C-T

58266935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277364-C-T

58267067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277449-A-G

58267377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277742-G-A

58267377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277742-G-C

http://identifiers.org/hco/16/GRCh38#58267417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96277768-C-A

58267417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277768-C-T

58267428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277779-G-A

58267428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277779-G-T

58267596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277940-A-G

58267636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277968-A-G

58267648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96277974-G-A

58267736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96278064-G-A

58267736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96278064-G-T

58267933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96278232-T-C

58268066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96278342-C-T

http://identifiers.org/hco/16/GRCh38#58268298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96278520-C-A

http://identifiers.org/hco/16/GRCh38#58268368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96278589-C-A

58268368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96278589-C-T

58268619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96278792-G-T

58268699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96278846-G-A

58268791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96278896-T-C

58278312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96283686-G-T

58278360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96283725-G-C

58278360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96283725-G-T

58278369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96283734-A-T

58278406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96283770-A-G

58278447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96283787-G-A

58278447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96283787-G-T

http://identifiers.org/hco/16/GRCh38#58278562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/8/GRCm39#96283899-C-A

58278562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: stop gained
orthologous variants: 96283899-C-G

58278562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: synonymous variant
orthologous variants: 96283899-C-T

58278673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96284042-T-C

http://identifiers.org/hco/16/GRCh38#58278678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96284047-C-A

58278967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96284332-T-C

58279000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96284405-T-C

58279154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96284708-C-T

58279286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96284899-T-G

58279395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96285064-G-T

58279607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: intron variant
orthologous variants: 96285304-T-G

58279839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: 96285513-T-C

58279839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: 96285513-T-G

58279879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: 96285556-T-C

58279879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: 96285556-T-G

http://identifiers.org/hco/16/GRCh38#58279890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96285568-C-A

http://identifiers.org/hco/16/GRCh38#58279892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96285570-A-C

58279892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: 96285570-A-G

58279892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: 96285570-A-T

http://identifiers.org/hco/16/GRCh38#58279894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96285572-C-A

58279894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: 96285572-C-G

58279894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: 96285572-C-T

http://identifiers.org/hco/16/GRCh38#58279928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96285626-C-A

58280077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: 96285776-A-G

58280077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3 prime UTR variant
orthologous variants: 96285776-A-T

58280389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 96286085-C-T

58280505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 96286195-C-G

58280505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 96286195-C-T

http://identifiers.org/hco/16/GRCh38#58280541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: http://identifiers.org/mco/8/GRCm39#96286231-C-A

58280628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 96286321-T-C

http://identifiers.org/hco/16/GRCh38#58280706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96286399-C-A

http://identifiers.org/hco/16/GRCh38#58280857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96286544-C-A

http://identifiers.org/hco/16/GRCh38#58281018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96286988-C-A

58281018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96286988-C-G

58281018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96286988-C-T

http://identifiers.org/hco/16/GRCh38#58281048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96287008-C-A

58281048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287008-C-T

http://identifiers.org/hco/16/GRCh38#58281163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96287181-C-A

58281186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287217-T-C

58281188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287219-G-A

58281188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287219-G-T

http://identifiers.org/hco/16/GRCh38#58281194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96287225-C-A

58281194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287225-C-T

58281222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 96287251-G-A

58281238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 96287267-A-T

http://identifiers.org/hco/16/GRCh38#58281275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96287301-A-C

58281311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 96287357-T-G

58281316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 96287362-G-A

58281372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287429-T-C

http://identifiers.org/hco/16/GRCh38#58281379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96287436-C-A

58281379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287436-C-T

58281397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287448-G-T

http://identifiers.org/hco/16/GRCh38#58281437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96287488-C-A

http://identifiers.org/hco/16/GRCh38#58281452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96287508-C-A

58281452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287508-C-T

58281494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287552-G-T

http://identifiers.org/hco/16/GRCh38#58281588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96287643-C-A

58281588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287643-C-T

58281602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287657-G-A

58281602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287657-G-T

58281633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287679-G-A

58281698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287750-G-A

58281731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287787-A-G

58281745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287801-A-G

http://identifiers.org/hco/16/GRCh38#58281767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96287823-C-A

58281767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287823-C-T

58281786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287841-A-G

http://identifiers.org/hco/16/GRCh38#58281805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96287859-C-A

58281827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287881-T-C

58281828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287882-G-T

58281853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287907-G-A

58281853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96287907-G-C

58282698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288225-G-A

58282698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288225-G-T

58282892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288425-G-T

58282940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288470-G-A

http://identifiers.org/hco/16/GRCh38#58282949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96288480-C-A

58282949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288480-C-G

58282949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288480-C-T

58282950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288481-T-A

58282994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288544-G-A

58283012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288562-A-G

58283075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288623-T-C

58283078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288626-T-A

58283081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288629-A-G

58283092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288642-T-C

58283107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288657-C-T

58283201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288751-T-C

http://identifiers.org/hco/16/GRCh38#58283226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96288776-A-C

58283226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288776-A-G

58283226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288776-A-T

58283229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288779-T-G

58283230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96288780-G-A

58283524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96289330-G-A

58283524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96289330-G-T

58283536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96289343-T-A

58283561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96289368-G-T

58283613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96289420-T-G

58283662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25002
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 96289470-C-T