124965731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33591898-T-C

http://identifiers.org/hco/3/GRCh38#124966366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33591253-C-A

http://identifiers.org/hco/3/GRCh38#124966502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33591028-A-C

http://identifiers.org/hco/3/GRCh38#124966569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33590884-C-A

124966750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33590676-A-G

124966858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33590572-A-G

124966882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33590549-A-G

124967099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33590342-T-C

124967149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33590295-T-C

124967222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33590236-T-C

124967232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33590226-C-T

124967291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33590179-G-A

124967291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33590179-G-T

124967682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589892-G-T

124967741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589869-C-T

124967814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589787-T-C

http://identifiers.org/hco/3/GRCh38#124967940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33589641-C-A

124967940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589641-C-T

http://identifiers.org/hco/3/GRCh38#124967943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33589634-C-A

124968009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589574-A-G

124968065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589525-G-T

124968084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589506-T-C

124968084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589506-T-G

124968164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589445-G-T

124968173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589435-G-A

124968173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589435-G-T

124968190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589415-T-C

124968190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589415-T-G

124968193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589412-T-C

http://identifiers.org/hco/3/GRCh38#124968260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33589351-C-A

124968260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589351-C-T

124968275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589336-T-C

124968328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589308-T-C

http://identifiers.org/hco/3/GRCh38#124968329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33589307-C-A

124968330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589306-T-C

124968375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589274-G-A

http://identifiers.org/hco/3/GRCh38#124968377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33589272-C-A

124968565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589089-T-C

124968594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33589024-G-T

124968599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588990-T-C

http://identifiers.org/hco/3/GRCh38#124968675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33588920-C-A

124968691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588904-G-T

124968712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588884-G-A

124968712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588884-G-T

124968716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588880-G-T

124968844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588755-G-A

124968997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588590-G-A

124968997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588590-G-T

124969027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588564-G-A

124969027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588564-G-T

124969039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588549-A-G

124969039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588549-A-T

http://identifiers.org/hco/3/GRCh38#124969103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33588506-C-A

124969130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588479-T-C

http://identifiers.org/hco/3/GRCh38#124969142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33588465-C-A

124969240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588385-C-T

124969390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588255-C-G

124969413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588232-G-C

124969413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588232-G-T

124969680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33588004-T-A

124969729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33587959-G-T

124970057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33587607-A-G

124970150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33587544-A-T

124970233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33587526-T-G

124970319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33587497-G-T

http://identifiers.org/hco/3/GRCh38#124970337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33587479-C-A

http://identifiers.org/hco/3/GRCh38#124970346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33587470-C-A

124970353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3 prime UTR variant
orthologous variants: 33587463-T-G

124970433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33587388-T-C

124970476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33587348-G-T

http://identifiers.org/hco/3/GRCh38#124970486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33587338-C-A

124970506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33587318-G-A

124970506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33587318-G-T

124970521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33587303-G-A

124970521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 33587303-G-T

124970577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 33587260-G-A

124970577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 33587260-G-T

http://identifiers.org/hco/3/GRCh38#124970608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33587226-C-A

124970608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 33587226-C-T

http://identifiers.org/hco/3/GRCh38#124970728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33587102-C-A

124970728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33587102-C-T

124970790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33587040-T-C

http://identifiers.org/hco/3/GRCh38#124971219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33585993-A-C

124971273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33585940-G-A

124971273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33585940-G-T

124971274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33585939-G-A

124971284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33585929-G-A

124972244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 33585393-G-T

124972248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 33585389-G-A

124972254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 33585383-A-G

124972349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 33585307-G-A

124972362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 33585293-A-T

124972639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 33585050-C-T

124973612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 33584061-C-T

124973618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 33584055-A-T

124973651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 33584038-T-C

124973695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 33584017-G-A

124973707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 33584005-T-C

http://identifiers.org/hco/3/GRCh38#124973948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33583755-A-C

124973958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33583744-G-A

124973958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33583744-G-T

124974553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33583252-T-A

124974553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33583252-T-C

124974559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33583245-A-G

124974654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33583160-G-A

124974754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33583070-G-C

124974784-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33583050-A-T

124974827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33583035-G-A

124975234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33582765-T-A

124975582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33582404-G-T

124975672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33582341-C-G

124975775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33582239-A-G

124975920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33582125-T-C

124975975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33582061-G-A

124976012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33582024-T-C

124976163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33581903-T-A

124977830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33581242-G-A

124977830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33581242-G-C

124977830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33581242-G-T

124977885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33581187-G-T

124977928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33581144-A-T

124977987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33581071-A-G

124978038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33581034-A-G

124978075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33581003-C-T

124979322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33580561-C-T

124979395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33580491-A-T

124979441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33580452-A-G

124979546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33580360-A-G

124983749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33576152-A-G

124983750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33576151-T-A

124983890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33576033-C-T

124983953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33575993-T-A

124983960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33575986-T-C

http://identifiers.org/hco/3/GRCh38#124984133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33575800-A-C

124984133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33575800-A-G

124984218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33575727-T-C

124984293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33575707-G-A

124984841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33575106-A-T

124984879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33575068-G-C

124985017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33574885-G-T

124985093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33574824-C-T

124985264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33574692-T-C

124985264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33574692-T-G

124985297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33574662-G-A

124985631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, undefined
orthologous variants: 33574409-T-C

124986029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33573994-C-T

124986030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33573993-G-A

124986144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33573889-T-C

124986150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33573883-G-T

124986373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, undefined
orthologous variants: 33573641-C-T

124986409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, undefined
orthologous variants: 33573605-C-T

124986638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, undefined
orthologous variants: 33573377-T-G

124986797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33573236-A-G

124986836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33573208-A-G

124986863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33573181-A-T

124989411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33572715-T-A

124989522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33572616-G-A

124989687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33572362-C-T

124989728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33572302-T-C

124989984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33572005-A-G

124990003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33571986-C-T

124990194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33571808-C-T

124990671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33571671-G-T

124990679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33571663-G-C

124991025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33570786-A-G

124991049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33570766-T-A

124991049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33570766-T-C

124992115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33570328-T-C

124992115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33570328-T-G

124993444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33566996-G-T

124993540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33566874-T-C

124993600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33566817-C-T

124993606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33566812-T-C

http://identifiers.org/hco/3/GRCh38#124993609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33566809-C-A

124993613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33566805-C-T

124993642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33566761-C-T

124993643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33566760-G-A

124993671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33566734-G-A

124993765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33566647-A-G

124993824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33566583-A-G

124993890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33566509-A-G

124995623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33565200-A-T

124995671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, undefined
orthologous variants: 33565161-T-G

http://identifiers.org/hco/3/GRCh38#124995716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33565117-C-A

124995716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33565117-C-T

http://identifiers.org/hco/3/GRCh38#124995740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33565107-A-C

124995808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33565041-G-A

124995815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33565028-C-T

124995846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33564421-A-G

124996470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33564112-T-A

124996470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33564112-T-C

124996509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33564075-A-G

124996616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33563973-G-A

124997162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33563403-T-C

124997232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33563339-A-G

124997255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33563317-C-G

124997750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33562803-A-G

124997832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33562720-G-T

124997871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33562684-T-C

124998164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33562463-G-A

124998164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33562463-G-C

124998212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33562395-C-T

124998255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33562350-G-A

124998335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33562285-T-G

http://identifiers.org/hco/3/GRCh38#124998464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33562141-C-A

124998506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33562104-C-T

124998672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33561890-A-T

124998763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33561790-G-A

124999351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33561249-C-T

124999415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33561185-G-A

124999806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33560822-A-T

124999930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33560700-A-G

124999983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33560647-A-G

125000007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33560623-C-T

125000141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33560489-T-C

125000617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33560052-A-T

125000825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33559864-G-A

125000994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33559694-A-G

125001680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33559245-T-A

125001680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33559245-T-C

125001725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33559213-A-T

125001771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33559169-A-G

http://identifiers.org/hco/3/GRCh38#125001833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33559110-C-A

125001995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense_variant, undefined
orthologous variants: 33558948-A-G

125001995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense_variant, undefined
orthologous variants: 33558948-A-T

125002007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33558936-G-A

125002007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33558936-G-T

http://identifiers.org/hco/3/GRCh38#125002287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#33558621-C-A

125002287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense_variant, undefined
orthologous variants: 33558621-C-T

125002465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33558450-G-T

125002574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33558360-T-A

125002702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33558226-C-T

http://identifiers.org/hco/3/GRCh38#125002917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33558011-C-A

125002917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33558011-C-T

125002951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33557989-T-A

125003154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33557805-C-T

125003212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33557751-G-C

125003897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, undefined
orthologous variants: 33557035-C-G

125003929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33557003-C-T

125004011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33556924-G-A

125004068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33556868-T-C

125004180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33556768-G-A

125004225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33556733-T-G

125004408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33556579-G-C

125005037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33556233-G-C

http://identifiers.org/hco/3/GRCh38#125005127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33556144-C-A

125005166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33556112-C-T

125005195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33556084-T-C

125005217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33556061-T-A

http://identifiers.org/hco/3/GRCh38#125005236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33556042-A-C

125005267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 33556010-T-C

125005290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33555987-T-G

125005356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33555921-A-G

http://identifiers.org/hco/3/GRCh38#125005509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33555780-C-A

125005509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33555780-C-T

125006179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33555710-G-A

125006179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33555710-G-T

125006217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33555672-T-C

http://identifiers.org/hco/3/GRCh38#125006357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33555543-C-A

125006559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33555316-T-A

125006568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33555307-C-T

125006666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33555209-T-G

125007683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33553398-G-A

125007739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33553346-C-T

125007858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33553233-T-C

125007858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33553233-T-G

125008366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33553044-G-A

125008388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33553006-C-T

125008468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33552929-T-A

125008468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33552929-T-C

125008841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33552890-T-C

125008920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33552812-G-C

125009028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33552707-C-G

125009100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33552635-T-C

125009369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33552359-A-G

125009400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33552330-C-T

125009532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33552222-T-A

125009532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33552222-T-C

125009532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33552222-T-G

125009533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33552221-G-A

125009533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33552221-G-C

125009533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33552221-G-T

125009555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33552199-T-A

125009559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33552195-G-A

125009559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33552195-G-C

125009559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33552195-G-T

http://identifiers.org/hco/3/GRCh38#125009781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33552010-C-A

125009781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33552010-C-T

125009815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 33551976-T-C

125009845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551946-G-A

125009845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551946-G-T

125009849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551942-A-T

125009854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551937-G-A

125009854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551937-G-T

http://identifiers.org/hco/3/GRCh38#125009919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33551883-C-A

125009969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551827-A-G

125010038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551760-T-G

125010152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551472-G-T

http://identifiers.org/hco/3/GRCh38#125010294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33551299-C-A

http://identifiers.org/hco/3/GRCh38#125010348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33551178-A-C

125010348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551178-A-T

125010376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551137-G-A

125010376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551137-G-C

125010376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551137-G-T

125010378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551129-T-C

125010378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33551129-T-G

125010509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33550891-G-A

125010509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 33550891-G-T

125010595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, undefined
orthologous variants: 33550819-G-A

125010595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, undefined
orthologous variants: 33550819-G-T

125010653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33550762-T-C

125010689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33550723-T-A

125010874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33550532-C-G

125010875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33550526-T-C

125010938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33550464-T-C

125010991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33550422-G-A

125011369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33549212-A-G

125011462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33549134-T-C

125011578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33549054-C-T

125011770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33548873-C-T

125011798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33548850-G-A

125011848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33548807-T-C

http://identifiers.org/hco/3/GRCh38#125011873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33548795-C-A

125011873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33548795-C-T

125012024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33548688-C-T

125012305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33548273-G-A

http://identifiers.org/hco/3/GRCh38#125012522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33548069-C-A

125012522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33548069-C-G

125012522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33548069-C-T

125012587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33547997-T-C

125012613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33547974-T-C

125012614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33547973-G-A

125012636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33547951-G-A

125012657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33547930-T-C

125012657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33547930-T-G

http://identifiers.org/hco/3/GRCh38#125012776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33547817-C-A

125012831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33547762-A-G

125012870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33547723-C-T

http://identifiers.org/hco/3/GRCh38#125012909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33547684-A-C

http://identifiers.org/hco/3/GRCh38#125013006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33547587-C-A

125013072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33547521-G-A

http://identifiers.org/hco/3/GRCh38#125013075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/16/GRCm39#33547518-A-C

125013105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33547488-T-A

125013105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33547488-T-C

125013250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33547331-C-G

125013250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33547331-C-T

125013263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33547318-A-G

125013267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33547314-T-C

125013271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33547310-G-A

125013389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33547192-T-C

125013389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33547192-T-G

125013396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33547185-G-A

125013396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33547185-G-C

125013416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33547165-T-G

125013431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33547150-T-C

125013491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33547111-C-T

http://identifiers.org/hco/3/GRCh38#125013560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33547045-C-A

125013560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33547045-C-T

125013564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33547041-G-A

125013564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: stop gained
orthologous variants: 33547041-G-T

http://identifiers.org/hco/3/GRCh38#125013654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33546984-A-C

125013654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33546984-A-G

125013654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33546984-A-T

125013771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33546867-T-A

125013771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33546867-T-C

125013771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33546867-T-G

125013835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33546824-C-T

125013904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33546755-A-G

125013914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33546745-G-A

125013915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33546744-G-A

125013915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33546744-G-T

125013967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33546692-C-T

125014029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546634-A-G

125014032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546631-A-G

125014035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546628-A-G

125014039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546624-T-G

http://identifiers.org/hco/3/GRCh38#125014040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33546623-C-A

http://identifiers.org/hco/3/GRCh38#125014054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33546609-A-C

125014054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546609-A-G

125014076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546588-T-C

http://identifiers.org/hco/3/GRCh38#125014083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33546585-C-A

125014083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546585-C-T

http://identifiers.org/hco/3/GRCh38#125014129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33546540-C-A

125014129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546540-C-G

125014129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546540-C-T

http://identifiers.org/hco/3/GRCh38#125014140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33546529-A-C

125014140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546529-A-G

125014140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546529-A-T

http://identifiers.org/hco/3/GRCh38#125014163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33546506-C-A

125014163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546506-C-T

125014465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546209-C-G

125014465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546209-C-T

125014531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546146-G-A

125014531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546146-G-C

http://identifiers.org/hco/3/GRCh38#125014637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33546073-A-C

http://identifiers.org/hco/3/GRCh38#125014640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33546071-A-C

125014640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546071-A-G

125014640-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546071-A-T

125014655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546056-G-A

125014655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546056-G-C

125014655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33546056-G-T

http://identifiers.org/hco/3/GRCh38#125014750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33545986-C-A

http://identifiers.org/hco/3/GRCh38#125014877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33545907-C-A

125014877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, missense_variant
orthologous variants: 33545907-C-G

125014877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, missense_variant
orthologous variants: 33545907-C-T

125014901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, missense_variant
orthologous variants: 33545883-G-T

http://identifiers.org/hco/3/GRCh38#125014940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33545850-C-A

125015032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33545778-G-A

125015039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33545771-T-A

125015039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33545771-T-C

125015046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33545767-T-C

125015050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33545763-G-A

125015050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33545763-G-T

http://identifiers.org/hco/3/GRCh38#125015059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33545762-C-A

125015059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33545762-C-T

http://identifiers.org/hco/3/GRCh38#125015261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33545640-C-A

125015261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33545640-C-T

125016195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33544100-G-A

125016239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33544060-G-A

125016239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33544060-G-C

125016429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33543632-C-T

125016600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33543357-C-T

125016624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33543333-G-A

125016813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33543008-G-A

125018709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33541992-T-C

125018723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33541978-G-A

http://identifiers.org/hco/3/GRCh38#125019560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33541054-C-A

125019560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33541054-C-T

125019645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33540971-G-A

125019645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33540971-G-T

125019713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33540922-G-A

125019713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33540922-G-T

http://identifiers.org/hco/3/GRCh38#125019744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33540887-C-A

125019795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33540837-A-G

125020033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33540617-T-C

http://identifiers.org/hco/3/GRCh38#125020066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33540584-A-C

125020090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33540560-T-C

125020477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33540484-C-T

125020746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33540255-G-T

125020927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33540078-G-A

125020989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33540016-G-A

125021010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33539995-G-A

125021049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33539956-G-A

125021049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33539956-G-T

125021149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33539855-T-C

125021149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33539855-T-G

http://identifiers.org/hco/3/GRCh38#125021289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33539710-A-C

125021341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33539663-G-C

125021461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33539520-G-C

http://identifiers.org/hco/3/GRCh38#125021517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33539470-A-C

125021656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33539341-G-A

125021899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33539103-G-T

125023829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33535446-G-T

125023859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33535416-C-G

125023859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33535416-C-T

125024061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33535252-C-G

125024061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33535252-C-T

125024079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33535234-A-G

125024122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33535190-T-C

125024135-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33535178-T-A

125024179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33535139-T-A

125024506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33534802-A-G

125024767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33534041-G-T

125024864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33533978-C-T

125024994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33533861-T-A

125026118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33532025-G-A

125026121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33532022-G-A

http://identifiers.org/hco/3/GRCh38#125026402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33531707-A-C

125026563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33531558-G-A

125026580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33531540-C-T

125027078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33531199-T-A

125027078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33531199-T-C

http://identifiers.org/hco/3/GRCh38#125027103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33531163-C-A

125027103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33531163-C-T

http://identifiers.org/hco/3/GRCh38#125027105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33531161-C-A

125027105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33531161-C-T

http://identifiers.org/hco/3/GRCh38#125027111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33531155-C-A

125027111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33531155-C-T

125027153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33531117-T-C

125027254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33531018-C-T

125027327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33530945-G-A

http://identifiers.org/hco/3/GRCh38#125027346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33530926-A-C

http://identifiers.org/hco/3/GRCh38#125027382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33530890-A-C

http://identifiers.org/hco/3/GRCh38#125027396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33530876-C-A

http://identifiers.org/hco/3/GRCh38#125027399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33530873-A-C

125027399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33530873-A-G

125027411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33530861-G-A

125027421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33530854-C-T

125027441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33530834-G-A

125027450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33530825-G-A

http://identifiers.org/hco/3/GRCh38#125027537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33530738-C-A

125027537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33530738-C-T

125028303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33528679-A-G

http://identifiers.org/hco/3/GRCh38#125028361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33528631-C-A

125028361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33528631-C-T

125028386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33528611-C-T

125028560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33528458-T-C

125028568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33528450-C-T

http://identifiers.org/hco/3/GRCh38#125028603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33528420-C-A

125028676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33528315-T-C

125028730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33528260-T-C

125028842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33528164-G-A

125028906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33528124-C-T

125028922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33528108-C-T

125029010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33528002-C-G

125029061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33527959-G-A

125029061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33527959-G-T

125029087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33527933-C-T

125029212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33527557-G-A

125029266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33527503-T-A

125029266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33527503-T-G

125029278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33527491-G-A

125029326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33527443-A-G

125029383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33527386-C-T

125029443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33527332-A-G

125029507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33527269-G-A

125029546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33527235-A-G

125031571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33526654-C-G

125031571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33526654-C-T

125032459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33525843-C-T

125032510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33525806-G-T

125032647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33525690-G-A

125032765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33525561-T-C

125033343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33525015-G-C

125033343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33525015-G-T

125033412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33524957-C-G

http://identifiers.org/hco/3/GRCh38#125033643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33524738-A-C

125036250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33522714-T-A

125036309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33522655-T-C

125036469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33522574-C-T

125037409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: -A-G

http://identifiers.org/hco/3/GRCh38#125037485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: -A-C

http://identifiers.org/hco/3/GRCh38#125037546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: -A-C

125037546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: -A-T

125037557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: -G-C

125037615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: -C-T

125037620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: -T-C

125039051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33521520-G-A

125039434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33521159-T-C

125039434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33521159-T-G

125039832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33520975-A-G

http://identifiers.org/hco/3/GRCh38#125039848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33520959-A-C

http://identifiers.org/hco/3/GRCh38#125039854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33520953-A-C

125039880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33520927-G-A

125039935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33520885-T-G

125040021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33520803-G-A

125040143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33520670-T-C

125040488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33520367-G-C

125040494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33520361-C-T

125040820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33520050-A-G

http://identifiers.org/hco/3/GRCh38#125041024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33519851-C-A

http://identifiers.org/hco/3/GRCh38#125041146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33519728-A-C

http://identifiers.org/hco/3/GRCh38#125041644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33519057-C-A

125041644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33519057-C-T

125041646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33519055-C-G

125041656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33519047-T-C

125041799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33518942-A-G

125041944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33518825-G-A

125041978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33518803-A-G

125041979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33518802-G-A

125042732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33518445-T-A

125042906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33518244-G-C

125042960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33518190-G-A

125042964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33518186-T-G

125042978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33518172-G-T

125043122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33518028-C-T

125043139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33518011-C-T

125043146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33518004-G-A

http://identifiers.org/hco/3/GRCh38#125043154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33517996-A-C

125043766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33517378-C-G

http://identifiers.org/hco/3/GRCh38#125044942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33516581-A-C

125045126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33516418-T-C

125045457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33515989-C-T

125045495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33515946-C-G

125045516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33515928-G-A

125045898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33515580-C-T

125046029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, undefined
orthologous variants: 33515292-T-C

125046147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33515169-C-T

125047018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33514711-G-A

125047169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33514581-G-A

125047205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33514543-A-G

125047668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33513664-T-C

125047668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33513664-T-G

125047758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33513609-C-G

125047786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33513581-C-T

125047792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33513575-G-A

125047873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33513495-G-A

125048090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33513281-A-G

http://identifiers.org/hco/3/GRCh38#125048345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33513028-A-C

125048887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33512432-G-A

125049134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33512153-C-T

125049148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33512140-G-T

125049270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33512035-T-C

125049327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33511966-C-G

125049537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33511746-C-T

http://identifiers.org/hco/3/GRCh38#125050588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33510524-A-C

125050606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33510506-A-G

125050833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33510255-T-C

125050848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33510230-G-A

125050952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33510117-C-T

125051047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33509770-G-A

125051061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33509759-G-C

125051356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33508949-G-A

125051510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33508803-G-A

125051510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33508803-G-C

125051515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33508798-C-T

125051585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33508721-G-A

125051585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33508721-G-T

125051611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33508699-T-A

http://identifiers.org/hco/3/GRCh38#125051929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33508411-C-A

125051944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33508396-T-G

http://identifiers.org/hco/3/GRCh38#125051960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33508380-C-A

125052294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron_variant, undefined
orthologous variants: 33508136-C-T

125052494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33507933-G-A

http://identifiers.org/hco/3/GRCh38#125052557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33507872-C-A

125052563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33507866-A-G

125052746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33507699-G-T

125053251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33507190-T-A

125053378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33507074-T-C

125053434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33507021-C-T

http://identifiers.org/hco/3/GRCh38#125054277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33506410-A-C

http://identifiers.org/hco/3/GRCh38#125054361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33506326-C-A

125054361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33506326-C-T

125054526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33506189-A-T

125054910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33505836-G-A

125055232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33505504-C-T

125055327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33505422-A-G

125055335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33505414-G-A

125055408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33505345-G-A

125055448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33505305-G-A

125055448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33505305-G-C

125055448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33505305-G-T

125055459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33505293-A-G

125055506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33505279-T-C

http://identifiers.org/hco/3/GRCh38#125055518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33505265-C-A

125055518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: intron variant
orthologous variants: 33505265-C-T

http://identifiers.org/hco/3/GRCh38#125055582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33505216-C-A

125055582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33505216-C-T

125055627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33505171-G-A

125055627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33505171-G-C

125055627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33505171-G-T

125055630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33505168-T-C

125055636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33505162-A-G

125055769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense_variant, undefined
orthologous variants: 33505107-G-A

125055769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense_variant, undefined
orthologous variants: 33505107-G-T

http://identifiers.org/hco/3/GRCh38#125055805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#33505071-C-A

125055805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33505071-C-G

125055805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33505071-C-T

125055833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: synonymous variant
orthologous variants: 33505043-G-A

125055833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33505043-G-C

125055833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33505043-G-T

125055835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33505041-G-A

125055835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: missense variant
orthologous variants: 33505041-G-T

125055931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 33504940-G-A

125055931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29227
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 33504940-G-T