112160456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 121506491-A-G

http://identifiers.org/hco/12/GRCh38#112160836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121506143-C-A

112160836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121506143-C-T

112160907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 121506087-A-G

112160917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 121506077-G-T

http://identifiers.org/hco/12/GRCh38#112160984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121506003-C-A

http://identifiers.org/hco/12/GRCh38#112161104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121505905-C-A

112161168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505842-G-A

112161168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505842-G-T

112161201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505811-G-A

112161201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505811-G-T

112161264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505755-G-T

http://identifiers.org/hco/12/GRCh38#112161270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121505749-C-A

112161270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505749-C-T

112161285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505733-G-A

112161285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505733-G-T

112161308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505712-G-T

112161407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505633-C-T

112161487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505552-A-G

112161586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505471-G-A

112161586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505471-G-T

112161697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505364-G-A

112161697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505364-G-T

112161698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505363-G-A

112161699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505362-C-T

112161703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505358-A-G

112161703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505358-A-T

112161714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505352-G-T

112161717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505349-A-G

112161817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505224-T-C

112161817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505224-T-G

112161860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505181-C-G

112161915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505124-C-T

112162025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505010-T-C

112162025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121505010-T-G

112162039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121504996-T-G

112162265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121504786-T-A

112162265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121504786-T-C

112162294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121504759-C-G

112162294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 121504759-C-T

112162611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121504470-G-A

112162611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121504470-G-T

112162831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121503309-T-C

112162885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121503260-G-A

112162885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121503260-G-T

112162906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121503243-C-T

112163080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121503112-G-A

112163113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121503079-T-A

112163176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121503016-T-C

112163393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121502860-A-G

112163431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121502828-G-A

112163431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121502828-G-T

112163470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121502805-G-T

112163627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121502707-G-A

112163636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121502698-G-A

112163636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121502698-G-C

http://identifiers.org/hco/12/GRCh38#112163690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121502644-A-C

112163690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121502644-A-G

112163763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121502571-G-A

112163763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121502571-G-T

112163789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121502554-T-C

112164238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121501841-T-C

http://identifiers.org/hco/12/GRCh38#112167245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121501050-C-A

112167245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121501050-C-T

http://identifiers.org/hco/12/GRCh38#112167253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121501042-C-A

http://identifiers.org/hco/12/GRCh38#112167467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121500850-C-A

112167467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121500850-C-T

112167542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121500775-G-T

112167654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121500702-C-T

http://identifiers.org/hco/12/GRCh38#112167672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121500689-A-C

112167672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121500689-A-G

112167672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121500689-A-T

112167678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121500683-G-A

112167678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121500683-G-T

http://identifiers.org/hco/12/GRCh38#112167679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121500682-C-A

112167729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121500648-G-T

112169559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121498792-C-T

112169574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121498777-T-A

112169722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121498657-G-T

http://identifiers.org/hco/12/GRCh38#112170192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121498428-C-A

112170192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121498428-C-T

http://identifiers.org/hco/12/GRCh38#112170195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121498425-C-A

112170195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121498425-C-G

112170195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121498425-C-T

http://identifiers.org/hco/12/GRCh38#112170213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#121498407-C-A

112170213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121498407-C-T

http://identifiers.org/hco/12/GRCh38#112170218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#121498402-C-A

112170218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121498402-C-T

112170248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121498375-A-G

http://identifiers.org/hco/12/GRCh38#112170395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#121498223-A-C

112170395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 121498223-A-G

112170443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 121498175-A-G

112170449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 121498169-A-G

112171097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 121497530-G-A

112171097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 121497530-G-T

http://identifiers.org/hco/12/GRCh38#112171348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121497285-C-A

112171408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121497225-C-T

http://identifiers.org/hco/12/GRCh38#112171412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121497221-C-A

112171412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121497221-C-T

http://identifiers.org/hco/12/GRCh38#112171467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121497176-C-A

112171467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121497176-C-T

112171506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121497162-T-C

112171552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121497047-T-C

112171995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121496761-C-T

112171996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121496760-C-T

http://identifiers.org/hco/12/GRCh38#112172344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121496619-C-A

112172449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121496520-C-T

112175951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121494188-T-A

112175951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121494188-T-C

112175986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121494162-G-A

112175986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121494162-G-C

112175986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121494162-G-T

http://identifiers.org/hco/12/GRCh38#112175992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121494156-C-A

112176165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121494011-A-G

112176473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121493817-A-G

http://identifiers.org/hco/12/GRCh38#112176579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121493747-C-A

112176719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121493607-T-A

112176738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121493589-G-A

112176738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121493589-G-T

112177103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121493307-G-A

112177179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121493237-A-T

112179093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121491864-C-G

112179093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121491864-C-T

112179161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121491796-G-A

112179164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121491793-G-A

http://identifiers.org/hco/12/GRCh38#112179417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121491530-C-A

112179417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121491530-C-T

112180667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121490145-A-G

112183144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 121488613-T-C

112183144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 121488613-T-G

112183172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121488585-A-G

http://identifiers.org/hco/12/GRCh38#112183184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121488573-C-A

112183184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121488573-C-G

112183306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121488451-G-C

112183306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121488451-G-T

http://identifiers.org/hco/12/GRCh38#112183309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121488448-C-A

112183309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121488448-C-G

112183778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121488115-T-G

112183812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121488083-A-G

112183954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121487980-G-A

112183954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121487980-G-C

112183954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121487980-G-T

112184093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121487878-T-A

http://identifiers.org/hco/12/GRCh38#112184166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121487806-C-A

112184166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121487806-C-G

112184215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121487758-C-T

112184216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121487757-G-A

112184396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 121487577-G-A

112184464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121487509-G-A

112184464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121487509-G-C

112184464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121487509-G-T

112184545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121487428-G-T

112184621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121487352-C-G

112184621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121487352-C-T

112185097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121486876-T-A

112185415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121486558-G-A

112185415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121486558-G-C

112185415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121486558-G-T

112185513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121486463-T-A

112185527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121486448-A-G

http://identifiers.org/hco/12/GRCh38#112185548-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121486427-A-C

112185557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121486418-T-A

112188525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121484311-G-A

112190812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121482897-A-G

112190875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121482834-G-A

112190875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121482834-G-T

112190959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, undefined
orthologous variants: 121482750-G-T

112191018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121482692-T-A

http://identifiers.org/hco/12/GRCh38#112191022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121482688-C-A

112191022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121482688-C-T

http://identifiers.org/hco/12/GRCh38#112191039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121482672-C-A

112191039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121482672-C-T

112192505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121481799-G-A

112192505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121481799-G-T

http://identifiers.org/hco/12/GRCh38#112192534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121481771-A-C

112192595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121481710-A-G

112192627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 121481678-T-C

112192863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121481494-T-A

112192863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121481494-T-C

112192907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121481451-T-C

112192926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121481432-T-C

112193225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121481116-G-T

112193340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121481024-C-T

112193488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121480897-T-A

112193488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121480897-T-C

112193546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121480839-C-G

112193546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121480839-C-T

112193599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121480786-G-A

http://identifiers.org/hco/12/GRCh38#112194979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121480021-C-A

112194979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 121480021-C-G

112195007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121479993-T-C

http://identifiers.org/hco/12/GRCh38#112195070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121479930-C-A

112195081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121479919-G-A

112195081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121479919-G-T

http://identifiers.org/hco/12/GRCh38#112195161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121479827-C-A

112195161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121479827-C-T

112195163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121479825-T-A

112195163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121479825-T-C

112195166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121479822-G-T

112195202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121479786-G-A

http://identifiers.org/hco/12/GRCh38#112200549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121477692-C-A

112200625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121477659-G-A

112200625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121477659-G-T

112200919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121477400-A-G

112200935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121477387-T-A

112200955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121477367-T-C

http://identifiers.org/hco/12/GRCh38#112200985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121477327-C-A

112202045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121475935-C-T

112202240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121476115-C-T

112202882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121475464-T-C

112202921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121475432-G-T

112202924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121475429-G-T

112203670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121474753-A-G

112203718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121474705-A-G

http://identifiers.org/hco/12/GRCh38#112203940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121474553-C-A

112204521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121472500-T-G

112204698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121472323-G-T

112204817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121472234-T-C

http://identifiers.org/hco/12/GRCh38#112207818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121471656-A-C

112207818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121471656-A-T

112207987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121471497-G-A

http://identifiers.org/hco/12/GRCh38#112208360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121471175-C-A

112208360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121471175-C-T

112209577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121470378-C-T

112209584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121470371-C-T

112209594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121470361-G-C

112209765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121470151-T-C

112209808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121470106-G-A

http://identifiers.org/hco/12/GRCh38#112209990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121469990-C-A

112209990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121469990-C-T

112210470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121469553-T-A

112210470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121469553-T-C

112212332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467813-C-T

http://identifiers.org/hco/12/GRCh38#112212354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121467791-C-A

112212354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467791-C-T

112212403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467753-G-A

112212403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467753-G-T

112212407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467749-G-C

112212407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467749-G-T

112212418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467738-T-C

112212434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467734-A-G

112212539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121467630-T-A

112212608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121467561-G-A

112212608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121467561-G-T

112212624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121467545-T-C

112212624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121467545-T-G

112212667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467502-G-A

112212673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467496-A-T

112212677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467492-A-G

112212677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467492-A-T

112216118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467379-C-G

112216191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467305-G-T

112216232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467264-T-C

112216425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467061-G-A

112216425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467061-G-T

http://identifiers.org/hco/12/GRCh38#112216426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121467060-C-A

112216426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121467060-C-T

112216917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121466428-G-A

112216957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121466387-G-A

112216967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121466376-G-A

112216979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121466364-G-A

112216981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121466362-T-C

112217014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121466327-T-C

http://identifiers.org/hco/12/GRCh38#112217043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121466298-C-A

112217043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121466298-C-T

112217113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121466228-G-A

112217113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121466228-G-T

112217152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121466189-A-G

112217203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121466137-A-G

112218613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121464044-C-T

112218642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121464014-T-C

112218768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121463916-T-C

112218969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121463736-T-C

112219014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121463693-G-A

112219080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121463634-G-C

112226797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121461940-G-T

112226833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121461906-T-C

112226907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121461860-G-A

112226907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121461860-G-C

112226907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121461860-G-T

112227942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460940-G-A

112227942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460940-G-T

112227950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460932-A-G

112227950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460932-A-T

http://identifiers.org/hco/12/GRCh38#112227982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121460901-C-A

112227982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460901-C-T

112228127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121460828-C-T

112228562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460478-C-T

112228570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460470-C-T

http://identifiers.org/hco/12/GRCh38#112228612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121460434-C-A

112228720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121460344-T-C

http://identifiers.org/hco/12/GRCh38#112228918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121460167-C-A

112228918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121460167-C-T

112229615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121459718-C-T

112229650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121459688-T-C

112229650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121459688-T-G

112229792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121459547-A-T

112229980-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121458931-T-A

112230160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121458728-T-C

112230165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121458723-T-C

http://identifiers.org/hco/12/GRCh38#112230196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121458593-C-A

112230538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121458277-G-A

112230538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121458277-G-T

http://identifiers.org/hco/12/GRCh38#112230636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121458207-C-A

112230636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121458207-C-T

112230850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121457998-A-G

112231023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121457271-G-A

112231023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121457271-G-T

112231095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121457201-T-C

112231106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121457191-A-G

http://identifiers.org/hco/12/GRCh38#112231116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121457181-C-A

112231187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121457126-T-C

112231187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121457126-T-G

112231193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121457120-C-G

112231193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121457120-C-T

112231389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121456957-A-G

http://identifiers.org/hco/12/GRCh38#112231716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: splice acceptor variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121456623-C-A

112231746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121456596-T-C

http://identifiers.org/hco/12/GRCh38#112231834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121456541-C-A

112232917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121455453-T-G

112232992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121455356-T-G

112232996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 121455352-G-A

112232996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 121455352-G-T

112233152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121455199-T-C

http://identifiers.org/hco/12/GRCh38#112233173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121455178-A-C

112233173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121455178-A-G

112233173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121455178-A-T

http://identifiers.org/hco/12/GRCh38#112233191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121455160-A-C

112233191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121455160-A-T

112235137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121453507-G-A

112235447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121453267-G-T

112235614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121453099-G-T

112236809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121452215-T-G

112236899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121452129-G-T

112236929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121452103-G-C

112236929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121452103-G-T

112236939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121452094-G-A

112236939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121452094-G-C

112236939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121452094-G-T

112236984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121452049-G-A

112236987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121452046-T-A

112237102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 121451931-C-T

112237119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121451914-A-T

112237157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121451880-G-T

112237212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121451785-T-C

112237212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121451785-T-G

112239345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121449597-T-C

112239513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121449281-A-G

112239513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121449281-A-T

112239555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121449227-A-T

112239884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121448745-G-A

112239884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121448745-G-T

http://identifiers.org/hco/12/GRCh38#112240162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121448467-C-A

112242809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121447591-G-A

http://identifiers.org/hco/12/GRCh38#112242989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121447433-C-A

112242989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121447433-C-T

112243336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121446974-T-G

http://identifiers.org/hco/12/GRCh38#112243475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121446835-C-A

112243475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: synonymous variant
orthologous variants: 121446835-C-T

112243559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121446754-G-A

112243559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121446754-G-T

112244066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121446240-T-G

http://identifiers.org/hco/12/GRCh38#112244290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121446020-C-A

112244290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121446020-C-G

112246807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121445647-A-G

112247048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121445436-G-A

http://identifiers.org/hco/12/GRCh38#112247112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121445372-C-A

112247112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121445372-C-T

112247113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121445371-T-C

http://identifiers.org/hco/12/GRCh38#112247206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121445303-C-A

http://identifiers.org/hco/12/GRCh38#112247311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121445238-C-A

112247311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121445238-C-T

112247323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121445226-T-C

112247395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121445164-T-C

http://identifiers.org/hco/12/GRCh38#112247400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121445159-C-A

112247400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121445159-C-G

112247400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121445159-C-T

112247619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121444924-A-G

http://identifiers.org/hco/12/GRCh38#112247981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121444247-C-A

112247981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121444247-C-T

http://identifiers.org/hco/12/GRCh38#112247989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121444239-C-A

112247989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121444239-C-T

112248011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121444221-A-G

112248011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121444221-A-T

http://identifiers.org/hco/12/GRCh38#112248024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121444208-C-A

http://identifiers.org/hco/12/GRCh38#112248034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121444199-A-C

112248034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121444199-A-T

112248039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121444194-C-G

112248077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121444156-T-C

112248471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121443774-G-A

112249546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron variant
orthologous variants: 121443102-T-A

http://identifiers.org/hco/12/GRCh38#112249659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121443007-C-A

112249785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121442892-G-T

112249860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121442819-G-T

112249862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121442817-G-A

http://identifiers.org/hco/12/GRCh38#112249940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121442751-C-A

112249970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121442722-C-T

112250024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121442680-T-C

112250024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 121442680-T-G

http://identifiers.org/hco/12/GRCh38#112250348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121442308-A-C

112250381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121442275-A-G

112250489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121442160-T-A

112250739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121441966-T-C

112250793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121441913-T-G

112250894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121441830-G-A

112250894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121441830-G-T

112251264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121441463-G-A

112251264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121441463-G-C

112251264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121441463-G-T

112252156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121441053-T-C

112252299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121440928-A-T

112252411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121440814-T-C

112252599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121440626-T-C

112253841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121440207-T-C

112253922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121440124-C-T

112254149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121439843-G-A

112254435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121439537-G-A

112254647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121439349-A-G

112254917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121438874-T-C

112255408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121438448-C-T

112255482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121438379-T-C

112255487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121438374-T-G

112255524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121438344-G-A

112255979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121438001-C-T

112255990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121437990-G-C

112256209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121437798-T-C

112256209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121437798-T-G

112256537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121437485-A-G

112256537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121437485-A-T

112256560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121437466-G-A

112256560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121437466-G-C

112256560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121437466-G-T

112256587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121437418-T-C

112256587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121437418-T-G

112258219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121436442-G-A

112258219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121436442-G-C

http://identifiers.org/hco/12/GRCh38#112258251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121436410-C-A

112258251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121436410-C-T

112258375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121436291-A-T

http://identifiers.org/hco/12/GRCh38#112258405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121436263-C-A

112258405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121436263-C-T

112258517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121436199-C-T

http://identifiers.org/hco/12/GRCh38#112258866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121435479-A-C

112258866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121435479-A-G

112258932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121435433-T-A

http://identifiers.org/hco/12/GRCh38#112258945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121435431-C-A

112258945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121435431-C-T

112258970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121435408-T-C

112259065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121435353-G-A

112259065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121435353-G-T

112260019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121434700-T-C

112260117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121434609-C-G

112261235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433602-G-T

112261250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433587-A-G

112261250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121433587-A-T

112261862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121433065-G-A

http://identifiers.org/hco/12/GRCh38#112261864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121433063-C-A

112261864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121433063-C-T

112262002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121432930-A-T

http://identifiers.org/hco/12/GRCh38#112262004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121432928-C-A

112263816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121431141-T-C

http://identifiers.org/hco/12/GRCh38#112264010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121430975-C-A

112264010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121430975-C-T

112264019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121430966-T-C

112264019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121430966-T-G

112264202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121430801-G-A

112264202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121430801-G-C

112264258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121430746-A-G

112264323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121430683-A-G

112264350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121430659-T-C

112264420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121430593-C-T

112264543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121430474-C-T

112264553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121430464-T-C

112264661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121430376-A-G

112265182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121430223-G-A

112265534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121429950-C-T

112265764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121429777-A-G

112265925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121429314-T-C

112266877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121427731-C-T

112267523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121427393-G-A

112267523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121427393-G-C

112267523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121427393-G-T

http://identifiers.org/hco/12/GRCh38#112267773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121427147-C-A

112269649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121424975-G-A

112269649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121424975-G-T

112269668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121424963-T-C

112269673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121424958-G-A

112269866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121424764-A-G

112269892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121424738-T-A

112269892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121424738-T-C

112270036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121424613-G-A

112270651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121423938-G-C

112270957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121423585-T-G

112273490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121420124-C-G

112273563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121420074-G-T

112273573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121420066-A-G

http://identifiers.org/hco/12/GRCh38#112273592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121420047-C-A

112273592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121420047-C-G

112273592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121420047-C-T

112273606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121420033-C-T

http://identifiers.org/hco/12/GRCh38#112273855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121419809-C-A

112273855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121419809-C-G

112273855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121419809-C-T

112274093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121419597-A-G

112274759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121419241-G-A

112274759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121419241-G-T

112275071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121419013-G-T

http://identifiers.org/hco/12/GRCh38#112275143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121418945-A-C

112275227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121418862-G-A

112275305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121418788-A-G

112275849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121417464-C-T

112275871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121417442-C-G

112275887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121417434-C-T

112276046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121417286-G-T

112276064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121417268-C-T

112276318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121417024-A-G

112276347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121416994-A-T

http://identifiers.org/hco/12/GRCh38#112279368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121415754-A-C

112279368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 121415754-A-G

112280513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121414686-G-A

112280607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121414504-A-G

112280608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121414503-T-C

http://identifiers.org/hco/12/GRCh38#112280706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121414415-C-A

http://identifiers.org/hco/12/GRCh38#112283394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121411575-A-C

112283956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121411030-T-C

112283959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121411027-T-C

http://identifiers.org/hco/12/GRCh38#112284638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121409459-A-C

112284732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121409369-C-T

http://identifiers.org/hco/12/GRCh38#112285340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121409142-C-A

112285340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121409142-C-G

112285340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121409142-C-T

112285644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121408921-C-T

112305408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121405077-C-G

http://identifiers.org/hco/12/GRCh38#112305424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121405065-C-A

112305826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121404693-C-T

112305933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121404587-A-G

http://identifiers.org/hco/12/GRCh38#112305962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121404561-C-A

112305962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121404561-C-T

112306187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 121404343-G-A

112306187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 121404343-G-C

112306187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 121404343-G-T

http://identifiers.org/hco/12/GRCh38#112306188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121404342-C-A

112306267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121404267-G-A

112306267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121404267-G-C

112306267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121404267-G-T

http://identifiers.org/hco/12/GRCh38#112306301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121404077-A-C

112306516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121403875-T-C

112308946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121401899-C-T

112308964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121401881-C-G

112308964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121401881-C-T

112309003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121401845-T-C

112309128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121401716-A-T

http://identifiers.org/hco/12/GRCh38#112309483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121400733-C-A

112309506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121400712-A-T

http://identifiers.org/hco/12/GRCh38#112309587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121400642-C-A

112309587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 121400642-C-G

112309715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121400508-T-C

112309803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121400247-A-G

112309898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121400144-G-A

112310248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121399841-G-T

112312409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121398658-G-T

112312892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121398117-T-C

112313073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 121397940-T-C

http://identifiers.org/hco/12/GRCh38#112313188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121397832-A-C

112313188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121397832-A-G

http://identifiers.org/hco/12/GRCh38#112313196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121397824-C-A

http://identifiers.org/hco/12/GRCh38#112313199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121397818-C-A

112314430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121396867-G-T

112314630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121396676-A-G

112314681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121396625-T-G

112314734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121396586-T-C

112315152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121396298-T-C

112315330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121396130-T-C

112315373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121396087-A-G

112315690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121395817-T-C

112317048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121393876-G-C

112317092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121393841-T-C

112318754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121392816-T-C

112318826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121392735-T-C

112319208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121392459-C-T

112319209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121392458-A-G

112319678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 121391986-T-C

112319797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121391865-T-C

112325528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121389975-A-T

112326248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121389562-T-A

112328524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-T

112328603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-G

http://identifiers.org/hco/12/GRCh38#112340818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121383977-C-A

112340818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121383977-C-T

112340879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121383924-C-T

112340882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121383921-A-G

112340971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121383847-A-T

112341078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121383738-T-A

112341097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121383726-A-G

112341135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121383688-T-C

112341138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121383685-T-C

112341580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121383271-G-A

112341736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121383119-T-C

112341805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121382892-A-G

112346596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121379674-T-C

112347086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121378699-T-G

112347181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121378619-T-C

http://identifiers.org/hco/12/GRCh38#112347578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121378320-C-A

112347715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121378184-G-C

112350857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121375060-G-A

112351074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121374929-G-A

112356168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121371969-G-A

112361200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121369472-A-T

112361204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121369468-A-G

112361319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121369331-C-T

112361362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121369263-T-C

112361396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121369239-A-G

112361428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121369204-C-T

112361621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121369103-C-G

112361693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121369040-G-A

112361777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121368964-C-T

112371215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121366276-A-G

112371230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121366266-G-A

112374792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121365432-G-A

112374871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121365359-A-G

112375004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121365183-A-G

112375152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121365049-A-G

112375205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121364912-C-T

112375209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121364900-T-C

112378594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121361049-C-T

112379378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121360405-A-G

112379400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121360383-T-C

112379417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121360366-G-A

http://identifiers.org/hco/12/GRCh38#112380758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121359803-A-C

112380874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121359686-T-G

112380974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121359605-C-T

112381108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121359501-C-T

http://identifiers.org/hco/12/GRCh38#112381188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121359418-C-A

112381274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121359265-C-T

112381519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121358931-G-A

112381738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121358804-G-A

112381775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 121358787-G-A

112381819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 121358765-C-T

112382097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121358573-G-A

112382106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121358555-G-A

112382106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121358555-G-T

112382112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121358549-G-A

112382112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121358549-G-C

112382112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: missense variant
orthologous variants: 121358549-G-T

http://identifiers.org/hco/12/GRCh38#112382217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121358480-C-A

112382217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 5 prime UTR variant
orthologous variants: 121358480-C-T

http://identifiers.org/hco/12/GRCh38#112382392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#121358307-C-A

112382392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 5 prime UTR variant
orthologous variants: 121358307-C-G

112382392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26611
most severe consequence: 5 prime UTR variant
orthologous variants: 121358307-C-T