96274386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3 prime UTR variant
orthologous variants: 127082666-A-G

96274518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3 prime UTR variant
orthologous variants: 127082549-G-A

96274518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3 prime UTR variant
orthologous variants: 127082549-G-T

96274537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3 prime UTR variant
orthologous variants: 127082530-G-T

96274544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3 prime UTR variant
orthologous variants: 127082523-G-A

96274544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3 prime UTR variant
orthologous variants: 127082523-G-T

96274583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3 prime UTR variant
orthologous variants: 127082490-A-G

96274685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3 prime UTR variant
orthologous variants: 127082405-G-T

96274797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127082306-T-C

96274799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127082304-C-T

http://identifiers.org/hco/2/GRCh38#96274838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127082269-A-C

96274838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127082269-A-G

96274838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127082269-A-T

http://identifiers.org/hco/2/GRCh38#96274890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127082203-C-A

96274890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127082203-C-G

96274890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127082203-C-T

96274926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 127082168-T-G

96275076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 127082066-C-T

96275239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127081907-G-A

96276817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080832-C-T

96276865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080785-G-T

96276881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080766-C-G

http://identifiers.org/hco/2/GRCh38#96277102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127080557-A-C

http://identifiers.org/hco/2/GRCh38#96277346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127080315-C-A

96277346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080315-C-G

96277346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080315-C-T

96277421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127080256-G-A

96277672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 127080020-T-C

http://identifiers.org/hco/2/GRCh38#96277726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127079967-A-C

96277973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127079718-C-T

http://identifiers.org/hco/2/GRCh38#96278181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127079546-C-A

96278181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127079546-C-T

http://identifiers.org/hco/2/GRCh38#96278184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127079543-A-C

96278379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127078988-G-T

96278432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127078909-T-C

96278441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127078902-C-T

96278771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127078603-A-G

http://identifiers.org/hco/2/GRCh38#96279060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127078316-C-A

96279172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127078212-A-G

96279351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127078048-G-C

96279351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127078048-G-T

http://identifiers.org/hco/2/GRCh38#96279446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127077991-C-A

96279446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077991-C-T

96279500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 127077937-A-G

96279572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077865-G-T

96279582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077855-A-G

96279655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077803-T-A

96279662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077796-G-A

96279662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077796-G-T

96279801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077656-T-C

96280089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127077576-T-C

http://identifiers.org/hco/2/GRCh38#96281379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127077328-C-A

96281379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077328-C-G

96281410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077306-C-T

96281436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077281-T-A

96281436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077281-T-C

96281437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077280-G-A

http://identifiers.org/hco/2/GRCh38#96281496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127077223-A-C

96281496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077223-A-G

96281751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077050-T-C

96281763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077038-T-A

96281782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127077019-C-T

96281817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 127076987-T-C

96281915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 127076889-G-T

96281929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 127076875-A-G

96281967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127076840-G-A

96281967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127076840-G-T

96282081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127076741-T-C

96282085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127076737-T-A

http://identifiers.org/hco/2/GRCh38#96282148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127076672-A-C

http://identifiers.org/hco/2/GRCh38#96282260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127076562-C-A

96282260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127076562-C-T

http://identifiers.org/hco/2/GRCh38#96282265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127076557-A-C

96282265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127076557-A-G

http://identifiers.org/hco/2/GRCh38#96282288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127076534-C-A

96282288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127076534-C-T

96282336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127076493-G-A

96282336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127076493-G-C

96282336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127076493-G-T

http://identifiers.org/hco/2/GRCh38#96282470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127076351-A-C

96282470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127076351-A-G

96283173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127075601-T-C

http://identifiers.org/hco/2/GRCh38#96283179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127075595-C-A

96283179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127075595-C-T

96283188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127075586-T-C

96283428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127075355-G-A

http://identifiers.org/hco/2/GRCh38#96283494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127075329-C-A

96283494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127075329-C-T

96283498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127075325-A-T

96283540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 127075271-C-T

96283750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127075065-C-G

96283770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127075045-T-C

96283982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 127074841-G-T

http://identifiers.org/hco/2/GRCh38#96284030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127074798-C-A

96284030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127074798-C-T

http://identifiers.org/hco/2/GRCh38#96284052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127074776-C-A

96284052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127074776-C-T

96284057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127074771-G-A

96284057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127074771-G-T

http://identifiers.org/hco/2/GRCh38#96284059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127074769-C-A

96284076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127074753-G-A

96284076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127074753-G-T

http://identifiers.org/hco/2/GRCh38#96284317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127074590-C-A

96284617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127074292-C-G

96284617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127074292-C-T

http://identifiers.org/hco/2/GRCh38#96284665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127074248-C-A

96284665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127074248-C-T

96284754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127074212-T-C

http://identifiers.org/hco/2/GRCh38#96284898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127074108-C-A

96284898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127074108-C-T

96285140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127073809-G-C

96285140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 127073809-G-T

96285205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 127073740-G-A

96285205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 127073740-G-T

96285383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073566-A-G

96285421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073530-A-G

96285422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073529-A-G

96285494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073482-A-T

http://identifiers.org/hco/2/GRCh38#96285498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127073478-C-A

96285498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073478-C-G

96285498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073478-C-T

96285518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073459-C-G

96285518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073459-C-T

96285619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073367-A-G

96285820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073195-T-C

96285889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127073127-T-G

96286294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127072622-G-C

96286587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127072336-A-G

96286656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127072273-G-A

96286657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127072272-T-C

http://identifiers.org/hco/2/GRCh38#96286659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127072270-C-A

96286873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 127072056-T-C

96286900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127072029-A-T

96286967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127071996-G-A

96286967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127071996-G-C

96287109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 127071855-T-C

96287333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127071621-G-T

96287522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 127071439-T-C

96287566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127071395-G-A

96287621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127071338-A-G

96287771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127071145-G-A

96288057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070916-G-A

96288057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070916-G-T

http://identifiers.org/hco/2/GRCh38#96288082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127070891-C-A

96288377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070781-G-A

96288475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070695-C-T

http://identifiers.org/hco/2/GRCh38#96288532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127070639-C-A

96288532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070639-C-T

96288580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070620-T-C

96288604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070598-A-T

http://identifiers.org/hco/2/GRCh38#96288777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127070431-A-C

96288777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070431-A-G

http://identifiers.org/hco/2/GRCh38#96288778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127070430-C-A

96288802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070403-G-A

96288802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070403-G-T

96288863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070342-A-T

96289027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 127070153-A-G

96289385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 127069789-G-C

96290075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127068659-A-G

http://identifiers.org/hco/2/GRCh38#96290099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127068635-C-A

96290099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127068635-C-T

96290194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127068546-G-A

96290194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127068546-G-C

96290194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127068546-G-T

96290267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127068461-T-C

96290290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127068438-G-T

96290426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: 127068301-G-A

http://identifiers.org/hco/2/GRCh38#96290447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127068280-C-A

96290447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: 127068280-C-T

96290535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127068192-C-G

96290596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127068140-G-A

96290628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127068109-G-T

96290644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127068093-T-C

96290736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: 127068003-T-C

96291036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127067710-A-T

http://identifiers.org/hco/2/GRCh38#96291110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127067642-A-C

96291144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127067611-G-A

96291371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127067130-A-G

96291529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127066978-G-A

96291702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127066685-G-T

96291711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127066676-G-T

96291875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: 127066524-T-C

96291995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127066393-G-A

96291995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127066393-G-T

http://identifiers.org/hco/2/GRCh38#96292313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127065969-C-A

96293179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127063967-A-G

96293241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127063927-G-A

96293247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127063922-C-G

96293349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: 127063823-T-G

96293442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: 127063730-C-T

96293604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127063616-T-C

96293605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127063615-G-T

96293625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127063598-G-T

96293642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127063576-G-A

96293642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127063576-G-T

96294815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127062444-T-C

96295070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127062182-A-G

96295072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127062180-G-A

96295082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127062170-G-A

96295461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127061144-T-C

96295914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127060835-C-G

96295914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127060835-C-T

http://identifiers.org/hco/2/GRCh38#96295981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127060806-A-C

96295981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127060806-A-G

96296111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127060746-C-T

96296313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127060608-T-C

http://identifiers.org/hco/2/GRCh38#96296459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127060500-C-A

96296459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127060500-C-T

96296466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127060493-G-A

http://identifiers.org/hco/2/GRCh38#96296502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127060457-C-A

96296502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127060457-C-T

96296918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059943-C-T

96297095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059768-T-C

96297144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059694-G-C

96297144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059694-G-T

96297151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059687-T-C

96297162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059676-T-A

96297162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059676-T-C

96297241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059601-T-C

http://identifiers.org/hco/2/GRCh38#96297242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127059600-C-A

96297339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059506-A-T

96297424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: 127059422-C-G

96297424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: 127059422-C-T

96297608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059253-C-T

96297610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059251-T-C

96297610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059251-T-G

http://identifiers.org/hco/2/GRCh38#96297757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127059111-C-A

96297778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059090-T-C

96297796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059072-T-A

96297831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127059039-G-T

http://identifiers.org/hco/2/GRCh38#96297914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127058939-A-C

96298182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127058725-A-G

96298557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127058417-C-T

http://identifiers.org/hco/2/GRCh38#96298558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127058416-A-C

96298558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127058416-A-G

http://identifiers.org/hco/2/GRCh38#96298766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127058212-C-A

96298766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127058212-C-T

96298772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127058157-C-G

96298772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127058157-C-T

96298903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: 127058031-G-A

96299031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127057922-C-T

96299080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127057878-G-C

96299080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127057878-G-T

96299090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127057867-A-G

http://identifiers.org/hco/2/GRCh38#96299116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127057841-C-A

96299290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127056858-G-A

96299290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127056858-G-T

96299313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127056839-A-G

96299315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127056837-C-G

96299315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127056837-C-T

96299345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: 127056807-C-T

http://identifiers.org/hco/2/GRCh38#96299487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127056654-C-A

http://identifiers.org/hco/2/GRCh38#96299508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127056635-A-C

http://identifiers.org/hco/2/GRCh38#96299543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127056600-A-C

http://identifiers.org/hco/2/GRCh38#96299554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127056589-C-A

96299554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127056589-C-T

96299555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127056588-T-C

96299568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127056587-G-T

96299771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127056385-G-A

96299852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127056318-T-C

96299885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127056304-G-A

96299890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127056298-C-T

96300896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127054414-A-G

96301455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127053774-C-G

96301455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127053774-C-T

96301482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127053749-A-G

http://identifiers.org/hco/2/GRCh38#96301811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127053436-C-A

96301811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127053436-C-T

96301955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127052905-C-G

96301955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127052905-C-T

96303202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: 127052740-T-C

96303226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: missense variant
orthologous variants: 127052716-T-C

96303502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127052466-T-C

http://identifiers.org/hco/2/GRCh38#96304096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127052188-A-C

96304636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127051127-T-C

96304636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127051127-T-G

96304640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127051123-G-T

96304657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127051109-A-T

96304666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127051100-T-C

96304684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127051076-T-A

96304684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127051076-T-C

http://identifiers.org/hco/2/GRCh38#96304934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127050827-C-A

96304934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127050827-C-T

96304985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127050802-G-A

96304985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127050802-G-T

96304986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127050801-T-A

96305000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127050787-T-A

96305016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127050767-A-G

96305088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127050712-G-C

96305088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127050712-G-T

96305127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, undefined
orthologous variants: 127050673-G-A

96305127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, undefined
orthologous variants: 127050673-G-T

96305161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, undefined
orthologous variants: 127050640-G-A

http://identifiers.org/hco/2/GRCh38#96305369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#127050480-A-C

96305370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127050479-T-A

96305370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127050479-T-C

96305377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, undefined
orthologous variants: 127050472-C-T

96305479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 127050370-A-G

96305594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127050260-A-G

96305602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, undefined
orthologous variants: 127050252-G-A

96305602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron_variant, undefined
orthologous variants: 127050252-G-T

96305697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30859
most severe consequence: intron variant
orthologous variants: 127050182-C-T