115958115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: non coding transcript exon variant
orthologous variants: 118903840-C-T

http://identifiers.org/hco/12/GRCh38#115958239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118903793-C-A

115958239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118903793-C-T

115958313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118903726-G-A

http://identifiers.org/hco/12/GRCh38#115958375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118903664-C-A

115958375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118903664-C-T

115958425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118903626-G-A

http://identifiers.org/hco/12/GRCh38#115958468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118903583-C-A

http://identifiers.org/hco/12/GRCh38#115958497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118903570-C-A

115958519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118903553-A-G

115958542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118903534-G-A

115958542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118903534-G-T

115958543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118903533-G-C

115958543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118903533-G-T

115959950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118902111-C-T

http://identifiers.org/hco/12/GRCh38#115959968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118902093-C-A

http://identifiers.org/hco/12/GRCh38#115959983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118902078-C-A

115960036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118902026-T-C

http://identifiers.org/hco/12/GRCh38#115960400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118901662-C-A

115960400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 118901662-C-G

http://identifiers.org/hco/12/GRCh38#115960639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118901480-C-A

115960726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 118901398-A-G

http://identifiers.org/hco/12/GRCh38#115960783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118901354-C-A

115960787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 118901350-G-T

http://identifiers.org/hco/12/GRCh38#115960982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118901163-C-A

115960982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 118901163-C-T

115961145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 118901008-G-T

115963031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118899773-A-G

115963375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118899491-T-C

115963376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118899490-G-T

115963482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118899386-T-C

http://identifiers.org/hco/12/GRCh38#115963529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118899339-A-C

http://identifiers.org/hco/12/GRCh38#115963532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118899336-C-A

115963532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118899336-C-T

115963538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118899330-G-A

115963538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118899330-G-C

115963568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118899297-T-A

115963568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118899297-T-C

115963600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118899268-G-A

115963600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118899268-G-T

115963724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118899171-A-G

115965868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118897524-G-A

115965889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118897503-T-A

115965889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118897503-T-G

http://identifiers.org/hco/12/GRCh38#115965970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118897433-A-C

115966352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118897070-A-G

115966367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118897054-A-G

115966371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118897050-C-T

115969199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118895069-T-C

115969233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118895046-A-G

http://identifiers.org/hco/12/GRCh38#115969432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118894858-A-C

115969868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118894708-G-A

115970301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118894315-A-G

115970537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118893832-T-A

115970537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118893832-T-C

115970722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118893650-A-G

115970722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118893650-A-T

115970874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118893538-G-T

115971068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118893342-T-G

115971210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118893233-C-G

115971317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118893123-C-T

http://identifiers.org/hco/12/GRCh38#115971421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118893030-A-C

115971496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118892956-G-A

http://identifiers.org/hco/12/GRCh38#115971950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118892601-A-C

115971968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118892583-C-T

115972287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118892280-G-A

115972287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118892280-G-T

http://identifiers.org/hco/12/GRCh38#115972464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118892133-C-A

http://identifiers.org/hco/12/GRCh38#115972484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118892111-C-A

http://identifiers.org/hco/12/GRCh38#115972485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118892110-C-A

115972485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118892110-C-T

115973113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118891822-C-T

115973431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118891594-C-T

115973775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118891308-A-T

115974156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118891031-C-T

http://identifiers.org/hco/12/GRCh38#115974824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118890349-C-A

115975051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118890147-A-G

115975668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118889664-A-G

115975819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118889513-G-T

115981325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118888603-T-A

115982308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118887941-T-C

115982334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118887922-C-T

http://identifiers.org/hco/12/GRCh38#115983058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118887129-A-C

115983079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118887106-G-A

115983079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118887106-G-T

115983347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118886820-T-C

115983351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118886816-G-A

http://identifiers.org/hco/12/GRCh38#115983666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118886573-C-A

115983889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118885870-G-A

115984137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118885617-T-C

115984139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118885615-T-C

115984252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118885502-G-A

115984252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118885502-G-T

http://identifiers.org/hco/12/GRCh38#115984506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118885327-C-A

115984506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118885327-C-G

http://identifiers.org/hco/12/GRCh38#115984575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118885265-A-C

115984575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118885265-A-G

http://identifiers.org/hco/12/GRCh38#115985404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118884488-C-A

115985451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118884448-T-C

115985595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118884330-T-C

http://identifiers.org/hco/12/GRCh38#115986156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118884017-A-C

115986232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118883959-T-A

http://identifiers.org/hco/12/GRCh38#115986381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118883813-A-C

115986381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118883813-A-G

http://identifiers.org/hco/12/GRCh38#115986537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118883660-A-C

115986537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118883660-A-G

115986809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118883407-C-T

115987082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118883278-G-C

115987096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118883267-A-G

115987331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118883026-G-A

115987352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118883010-T-A

115987352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118883010-T-C

http://identifiers.org/hco/12/GRCh38#115987440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
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#118882958-A-C

115990540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118881249-G-A

115990769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118881047-A-G

115990903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118880903-T-A

115990989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 118880869-T-C

115991185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118880673-C-T

115991203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118880655-G-A

115991205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118880653-T-C

115991285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118880573-T-A

115991526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118880320-G-A

115991823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118880023-G-A

115992135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118879757-G-C

115992202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118879689-T-C

115992238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118879627-G-A

115992292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118879582-T-C

115992512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118879398-A-G

115992679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118879285-A-T

115992798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118879199-G-C

http://identifiers.org/hco/12/GRCh38#115993964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118878514-C-A

115994061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118878413-A-G

115995102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118877910-A-G

115996981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118876625-C-G

115997772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118876206-C-T

115997941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118876050-A-G

115998230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118875738-T-C

115998252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 118875716-G-T

115998435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118875555-T-C

115998514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118875465-G-T

115998557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118875425-G-T

116003136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118871988-C-T

116003178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118871955-T-A

116003178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118871955-T-C

116003178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118871955-T-G

116003441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118871760-T-C

116003528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118871699-C-T

116003855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118871256-C-T

116004699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118870470-C-T

116004728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118870441-T-A

116004813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118870357-T-C

116004889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118870284-C-T

116004925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118870256-A-T

116005236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118869964-A-G

116005282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118869920-A-G

116005319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118869883-G-A

116005728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118869639-C-T

116005811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118869563-T-C

116005811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118869563-T-G

116005879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118869505-T-C

116006438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118868948-A-T

116006541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118868848-A-T

116006562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118868827-G-C

http://identifiers.org/hco/12/GRCh38#116006796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118868629-C-A

116006825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118868601-T-C

http://identifiers.org/hco/12/GRCh38#116007005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118868450-C-A

116007005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118868450-C-G

116007005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118868450-C-T

116007162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118868300-T-C

116007217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118868246-A-T

116007270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118868195-G-A

116007270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118868195-G-T

116007350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118868113-T-A

116007350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118868113-T-C

116007511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118867958-T-C

116007666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118867791-G-A

116007666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118867791-G-C

116007666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118867791-G-T

http://identifiers.org/hco/12/GRCh38#116008076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118867237-C-A

116008076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118867237-C-G

116008185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118867138-T-C

116008608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118866735-A-G

http://identifiers.org/hco/12/GRCh38#116008628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118866715-C-A

116008628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 118866715-C-G

116008717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118866626-G-T

116008757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118866586-T-C

http://identifiers.org/hco/12/GRCh38#116008765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118866578-A-C

http://identifiers.org/hco/12/GRCh38#116008779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118866564-A-C

116008806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118866537-G-A

116009149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118866195-C-T

116009293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118866048-T-C

116009543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118865865-T-C

116009591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118865818-A-T

116009779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118865640-T-C

116009779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118865640-T-G

116009865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118865558-G-A

116009968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118865461-T-C

116009989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118865441-T-C

http://identifiers.org/hco/12/GRCh38#116010142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118865290-A-C

116010142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118865290-A-G

116010147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 118865285-A-G

http://identifiers.org/hco/12/GRCh38#116010241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118865193-A-C

116012685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118864483-C-G

116012737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118864451-T-A

116012737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118864451-T-C

116012738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118864450-G-C

116012738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118864450-G-T

http://identifiers.org/hco/12/GRCh38#116012862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118864363-A-C

116012884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118864341-G-A

116013760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118863742-T-G

116013860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118863649-C-T

http://identifiers.org/hco/12/GRCh38#116013885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118863630-A-C

116014022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118863505-T-C

116015373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118861972-G-C

116015373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118861972-G-T

http://identifiers.org/hco/12/GRCh38#116019213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118860012-A-C

116019310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 118859915-C-T

116019418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 118859822-A-G

116019512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118859762-A-G

116020045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118859394-T-C

116022248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118856876-A-T

116022428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118856725-G-A

116022428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118856725-G-C

116022439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118856714-G-C

116022706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118856456-T-A

116023186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118856039-C-T

116023280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118855917-A-G

116023282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118855915-C-T

116023453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118855697-A-G

http://identifiers.org/hco/12/GRCh38#116023465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118855684-C-A

116023622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118855549-T-A

116023638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118855534-G-C

116023718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118855458-A-G

116023754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118855421-C-T

116024128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118855118-A-G

116024134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118855112-A-G

116027737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118854158-T-C

116027859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118854034-T-C

116036449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118850111-A-G

116038729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118848197-A-T

116039237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118847767-G-T

116039456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118847553-C-T

116042602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118845395-A-T

116042663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118845338-G-A

116044071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118844092-T-C

116044129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118844037-C-T

116044130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118844036-C-T

116044132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118844034-G-A

116044132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118844034-G-T

116044172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118843992-G-A

116044882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118843510-A-G

116044987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118843396-T-A

116044987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118843396-T-C

116045028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118843356-C-T

116047807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118841388-G-A

116047816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118841379-A-G

116054557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118838345-G-A

116054632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118838275-G-C

116065617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118834930-T-C

116072947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118831780-C-T

116086753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118825535-T-C

116087329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118824457-C-T

http://identifiers.org/hco/12/GRCh38#116087530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118824316-C-A

116087787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118824113-C-T

116088350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118823528-T-C

116088438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118823470-C-T

116088500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118823415-G-C

116088549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118823366-C-T

116088694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118823294-A-G

116089728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118820712-T-C

116089864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118820592-A-T

116095739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118819594-T-C

116096027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118819329-T-C

116096041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118819316-C-T

116096620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118819099-C-T

116096786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118818917-T-C

116096800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 118818904-T-C

116097048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118818704-A-G

116097124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118818643-T-C

116098373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118818150-A-G

http://identifiers.org/hco/12/GRCh38#116098640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118817893-C-A

http://identifiers.org/hco/12/GRCh38#116101573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118816364-C-A

116101579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118816357-G-A

116101579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118816357-G-C

116101623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118816295-A-G

http://identifiers.org/hco/12/GRCh38#116102262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118815743-C-A

116102340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118815664-T-C

116103120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118815333-C-T

116103908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118814872-C-T

116104735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118814514-T-C

116104999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118814243-T-C

116105000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118814242-A-G

116105132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118814118-T-C

116105296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118814002-G-C

116105335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118813966-G-T

116105501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118813811-C-G

116105594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118813725-A-G

116105607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118813712-C-T

116105943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118813505-C-T

116106060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118813387-G-A

116106130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118813346-G-A

116106344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118813189-T-G

116107022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118812546-G-A

116107045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118812523-C-T

116107261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118812397-T-A

116107326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118812333-A-G

116109357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118811235-A-G

116109516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118811107-T-C

116109560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118811069-T-C

116109662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 118810997-T-C

http://identifiers.org/hco/12/GRCh38#116109693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118810963-A-C

116110333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118810222-T-C

116110641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118809855-C-G

116110671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118809829-G-A

http://identifiers.org/hco/12/GRCh38#116110809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118809706-C-A

116110921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118809596-T-C

http://identifiers.org/hco/12/GRCh38#116111232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118809326-A-C

116111232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118809326-A-G

http://identifiers.org/hco/12/GRCh38#116111321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118809256-C-A

116111356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118809228-T-C

http://identifiers.org/hco/12/GRCh38#116111522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118809066-A-C

116111522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118809066-A-G

116111626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118808962-T-C

116111692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118808896-C-T

116112195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118808482-T-A

116120963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118807925-A-G

116121000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118807888-A-G

116121199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118807697-T-G

116121559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118807427-A-G

http://identifiers.org/hco/12/GRCh38#116121618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118807380-C-A

116121618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118807380-C-G

116121706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118807288-G-A

116121856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118807147-G-C

http://identifiers.org/hco/12/GRCh38#116122062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118806937-A-C

116122531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118806496-T-C

116122931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118806081-C-T

116123354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118805664-T-C

116123394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118805510-T-C

116123486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118805427-A-G

116123568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118805343-G-A

116123849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118805096-A-G

116124195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118804776-T-A

116124405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118804578-T-C

116127069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118802671-G-A

116127225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118802529-A-G

116128573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118801762-T-C

116128602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118801730-G-C

116128947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118801444-A-T

116128998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118801332-G-A

116130235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118800440-T-C

116130591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118800151-T-A

116131037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118799710-A-G

116131037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118799710-A-T

116131164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118799577-A-G

116131186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118799558-T-C

116137048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118796003-T-C

116137295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118795831-T-C

http://identifiers.org/hco/12/GRCh38#116137380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118795754-A-C

116137423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118795714-G-A

http://identifiers.org/hco/12/GRCh38#116137516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118795630-C-A

116137650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118795539-T-C

116137725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118795458-C-G

116138251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118795251-C-T

116138405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118795155-A-G

116138405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118795155-A-T

116138551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118795040-T-G

http://identifiers.org/hco/12/GRCh38#116138794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118794837-A-C

116140603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118793886-A-T

116140923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118793655-T-C

116140928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118793650-C-T

116140933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118793645-G-A

116141347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118793228-T-C

116141732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118792903-C-T

116142013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118792703-A-G

116142964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118792021-T-C

116143033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118791941-G-A

116143771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118790535-A-G

116144148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118790212-C-G

116144511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118789946-C-G

116147557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118787296-G-A

http://identifiers.org/hco/12/GRCh38#116147579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118787274-A-C

116147599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118787256-T-C

116147626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118787219-T-C

116147909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118786937-T-C

116147975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118786866-C-G

116147975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118786866-C-T

116148077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118786766-G-A

116148077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118786766-G-C

116148084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118786731-G-A

http://identifiers.org/hco/12/GRCh38#116148152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118786632-C-A

116149421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118785963-T-C

116149581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118785806-C-T

116149701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118785701-G-C

116149996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118785355-T-A

116150020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118785317-G-A

116150047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118785290-C-T

http://identifiers.org/hco/12/GRCh38#116150422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118784925-A-C

116151248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118784277-T-G

116151370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118784159-A-G

116151801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118783640-T-C

116151853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118783609-C-T

116151966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118783534-C-T

116151996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118783504-T-C

116152356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, undefined
orthologous variants: 118783098-G-C

116152384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, undefined
orthologous variants: 118783068-G-T

116152479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, undefined
orthologous variants: 118782990-G-A

116152585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118782918-A-T

116153693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118781528-C-T

116153694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118781527-A-G

116153755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118781463-A-G

116153782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118781436-T-C

116153816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118781403-T-C

116153844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118781378-T-G

116154195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118780802-T-C

116154225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118780789-G-C

116155896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118779552-G-A

116155953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118779492-C-T

116155978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118779467-C-T

116156206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118779246-T-G

116156310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118779147-T-C

116156313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118779144-A-G

116156446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118779052-T-A

116156446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118779052-T-C

http://identifiers.org/hco/12/GRCh38#116158935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118777811-A-C

116159304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118777410-A-G

116159655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118777067-T-C

116159958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118776783-T-C

116160097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118776460-T-C

116160358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118776236-G-A

116160484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118776074-G-A

116160541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118776016-C-G

116167410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118772442-G-C

116167501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118772381-T-C

116168018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118771823-T-C

116171355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118769817-T-C

116171497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118769661-T-A

116171746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118769484-T-C

116171796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118769440-G-A

116172184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118768944-A-G

116172406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118768719-T-C

116172569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118768588-G-C

116172622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118768533-G-A

116175277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118767677-T-C

116178409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118765791-T-C

http://identifiers.org/hco/12/GRCh38#116178434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118765780-C-A

http://identifiers.org/hco/12/GRCh38#116178711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118765569-C-A

http://identifiers.org/hco/12/GRCh38#116180631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118764031-C-A

116180668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118763987-G-A

116180668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118763987-G-T

116180870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118763823-T-A

116180870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118763823-T-C

116183847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118762115-A-G

116183857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118762110-A-T

116183918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, undefined
orthologous variants: 118762053-T-C

116183926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, undefined
orthologous variants: 118762049-T-C

116184650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118761364-T-C

116184650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118761364-T-G

116185240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118760766-G-A

116185240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118760766-G-C

116185308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118760714-G-A

116185468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, undefined
orthologous variants: 118760572-T-C

116185715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118760415-A-T

116185730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118760408-T-A

116186125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118759902-T-A

http://identifiers.org/hco/12/GRCh38#116186177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118759848-A-C

116186227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118759798-T-A

116186227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118759798-T-C

116186295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118759731-C-T

116186519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118759537-A-G

116186723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118759376-G-T

116186943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118759167-C-T

116187670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118757543-T-C

http://identifiers.org/hco/12/GRCh38#116188301-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118756814-A-C

116188337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118756772-G-A

116188608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118756541-C-T

116188648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118756506-T-C

116189053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118756150-T-C

116193603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118753009-T-A

116193603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118753009-T-C

116193603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118753009-T-G

116197767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118752252-A-G

116197783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118752236-A-G

116197806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118752195-C-T

116198659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118751611-A-G

116198808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118751471-T-C

116198940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118751335-T-A

116199120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118751185-G-A

http://identifiers.org/hco/12/GRCh38#116201322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118749803-A-C

116201438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118749694-C-T

116201474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118749656-A-G

http://identifiers.org/hco/12/GRCh38#116202096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118749181-A-C

116202334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118748942-T-C

116202456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118748873-A-G

116202457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118748872-T-C

116202585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118748776-T-C

116202832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118748615-T-C

116203045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118748410-G-A

http://identifiers.org/hco/12/GRCh38#116204081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118747983-A-C

116204081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118747983-A-G

116204115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118747949-C-T

116204199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118747909-A-G

116204250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118747882-G-A

http://identifiers.org/hco/12/GRCh38#116204302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118747833-C-A

116204302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118747833-C-T

116204313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118747822-G-A

http://identifiers.org/hco/12/GRCh38#116204327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118747808-C-A

116204327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118747808-C-T

http://identifiers.org/hco/12/GRCh38#116204338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118747797-C-A

116204383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118747754-T-C

116204564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118747600-G-A

116204564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118747600-G-C

116204934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118747329-C-T

116208440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118745672-T-C

http://identifiers.org/hco/12/GRCh38#116208450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118745662-C-A

116208450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118745662-C-G

116208450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118745662-C-T

116208511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118745606-T-C

116209552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118744944-T-C

116210044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118744544-C-T

116210820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118743699-T-A

116210820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118743699-T-G

116212475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118742849-C-T

http://identifiers.org/hco/12/GRCh38#116214436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118742069-A-C

116214629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118741876-A-G

116214911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118741619-C-G

116214985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118741582-G-T

116218274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118741304-T-C

116221626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118739469-G-A

116221626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118739469-G-C

116225757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118738704-A-G

http://identifiers.org/hco/12/GRCh38#116225878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118738561-C-A

116225878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118738561-C-T

116226105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118738377-A-T

http://identifiers.org/hco/12/GRCh38#116226178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118738304-C-A

116226221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118738284-T-C

116226988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118737910-T-A

http://identifiers.org/hco/12/GRCh38#116227048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118737853-C-A

116227158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118737758-C-T

116229100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118736998-A-G

116229360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118736548-T-C

http://identifiers.org/hco/12/GRCh38#116229377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118736536-A-C

116229377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118736536-A-G

116236111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118733284-T-C

116236489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118732936-A-G

116236559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118732873-T-G

116237138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118732287-T-C

116237292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118731809-T-A

116237774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118731323-T-C

116238373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118730300-C-G

116238394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118730282-T-G

116238414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118730260-T-C

http://identifiers.org/hco/12/GRCh38#116241461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118729243-A-C

116241855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118728848-G-A

116241855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118728848-G-C

116242264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118728351-C-T

116242390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118728231-T-A

116243338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118727459-A-G

116243772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118727122-G-A

116243772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118727122-G-T

116243836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118727056-C-T

116243872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118727022-T-C

116244080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118726807-A-T

116244200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118726697-T-C

116244348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118726511-C-T

116244371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118726487-T-A

116244371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118726487-T-C

116244441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118726416-G-A

116244508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118726353-A-G

116258044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118715263-C-T

116258498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118715004-C-T

116258648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118714928-G-A

116258856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118714825-T-A

116259140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118714547-A-G

116259145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118714542-T-C

116259238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118714431-G-C

116259243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118714427-T-C

116259829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118713834-G-A

116259860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118713803-T-A

116259930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118713734-T-C

116259978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118713681-A-G

116260026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118713641-G-C

116260266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118713431-C-T

http://identifiers.org/hco/12/GRCh38#116260292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118713405-A-C

116260422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118713276-G-A

116261079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118712495-G-A

116261214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118712376-G-A

116261233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118712348-T-A

116261235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118712346-C-T

116261675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118711752-T-C

116261941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118711560-C-G

116261965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118711553-A-G

116262713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118710871-T-G

116262781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118710804-A-T

116262783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118710802-G-A

116262800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118710781-A-G

116262846-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118710736-T-A

116263272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118710016-A-G

116265233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118708539-A-G

116265843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118707916-T-C

116266449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118707321-T-C

116266520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118707251-C-G

116266535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118707236-A-G

116266582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118707190-G-A

116266588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118707184-G-A

116266617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118707146-T-C

116267068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118706731-T-C

116267068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118706731-T-G

http://identifiers.org/hco/12/GRCh38#116267279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118706548-A-C

116267619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118706254-T-A

116267619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118706254-T-C

http://identifiers.org/hco/12/GRCh38#116267713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118706146-A-C

116268893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118705151-T-A

116269794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118704622-G-T

116269909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118704510-C-G

116269909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118704510-C-T

116269967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118704464-A-T

116271752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118703626-T-A

116271752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118703626-T-C

116271820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118703556-A-T

116271924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118703478-A-G

http://identifiers.org/hco/12/GRCh38#116272047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118703376-C-A

116272047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118703376-C-G

116274225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118701863-G-A

116274243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118701842-T-A

http://identifiers.org/hco/12/GRCh38#116274367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118701720-A-C

http://identifiers.org/hco/12/GRCh38#116274398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#118701686-A-C

116274408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118701677-G-A

116274408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118701677-G-C

116274408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 118701677-G-T

116274563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118701537-T-C

116274563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118701537-T-G

116274963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118700979-T-A

116274963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118700979-T-C

116275027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118700941-C-T

116275082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118700881-A-G

http://identifiers.org/hco/12/GRCh38#116275160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118700785-A-C

116275192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118700747-T-G

116275250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118700693-T-A

116275964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 118699972-C-G

116276472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 118699483-A-G

http://identifiers.org/hco/12/GRCh38#116276584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#118699365-C-A

116276584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 118699365-C-T

http://identifiers.org/hco/12/GRCh38#116277019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118698952-C-A

116277019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118698952-C-G

116277019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118698952-C-T

http://identifiers.org/hco/12/GRCh38#116277036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#118698944-C-A

116277036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: intron variant
orthologous variants: 118698944-C-T

116277076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 118698904-G-A

116277076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 118698904-G-C

116277076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 118698904-G-T

116277106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 118698874-G-A

116277106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 118698874-G-T

116277324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 5 prime UTR variant
orthologous variants: 118698689-G-C

116277325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22962
most severe consequence: 5 prime UTR variant
orthologous variants: 118698688-G-C