127940655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32459692-A-G

127940692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32459661-A-G

127940799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32459586-G-T

127941064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32459345-G-A

127941093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32459332-G-A

127941093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32459332-G-C

127941138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32459312-A-G

http://identifiers.org/hco/9/GRCh38#127941182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32459268-C-A

http://identifiers.org/hco/9/GRCh38#127941302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32459118-C-A

127941361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32459076-C-T

127941372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32459065-A-G

127941400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32459045-G-A

127941400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32459045-G-T

127941620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458844-T-C

http://identifiers.org/hco/9/GRCh38#127941710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32458758-C-A

127941750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458726-G-A

127941790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458687-A-G

127941912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458583-A-G

127941973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458525-A-G

127941974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458524-A-T

127942037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458454-G-A

127942037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458454-G-T

127942069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458433-C-T

127942150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458392-A-G

127942175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458368-C-T

127942207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458332-T-C

127942226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458313-G-T

http://identifiers.org/hco/9/GRCh38#127942366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32458149-A-C

127942391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458123-G-A

127942391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458123-G-T

127942476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458058-C-G

127942476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32458058-C-T

127942566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32457976-T-C

127942566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32457976-T-G

127942785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32457780-G-A

127942785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32457780-G-T

127942828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32457740-T-A

127942828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32457740-T-C

127942828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32457740-T-G

127943041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32457581-G-A

127943041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32457581-G-T

127943122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32457521-T-G

127943159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32457484-G-T

http://identifiers.org/hco/9/GRCh38#127943284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32457363-C-A

127943315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32457342-G-T

http://identifiers.org/hco/9/GRCh38#127943341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32457318-C-A

127943369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32457293-C-T

http://identifiers.org/hco/9/GRCh38#127943448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32457190-C-A

127943448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32457190-C-T

127943464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32457161-G-A

127943464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32457161-G-T

127943527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32457100-A-G

127943732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32456976-G-A

127943732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32456976-G-T

127943743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32456965-G-A

127943862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32456895-G-T

127944533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32456612-G-C

127944533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32456612-G-T

127944549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32456611-G-A

127944549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32456611-G-T

http://identifiers.org/hco/9/GRCh38#127944577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32456578-C-A

127944577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32456578-C-T

http://identifiers.org/hco/9/GRCh38#127944578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32456577-C-A

127944578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32456577-C-T

127944744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32456437-T-C

http://identifiers.org/hco/9/GRCh38#127944934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32456254-C-A

127944934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32456254-C-T

127944970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32456222-A-G

http://identifiers.org/hco/9/GRCh38#127944976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32456216-C-A

127944976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32456216-C-T

http://identifiers.org/hco/9/GRCh38#127945014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32456179-C-A

127945014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32456179-C-T

http://identifiers.org/hco/9/GRCh38#127945048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32456145-C-A

127945123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32456079-C-T

127945279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455938-G-A

127945310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455881-T-C

http://identifiers.org/hco/9/GRCh38#127945316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32455875-C-A

127945316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455875-C-T

http://identifiers.org/hco/9/GRCh38#127945322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32455869-C-A

127945322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455869-C-T

127945328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455863-A-G

127945344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455837-G-A

127945344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455837-G-C

127945344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455837-G-T

http://identifiers.org/hco/9/GRCh38#127945390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32455791-C-A

127945390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32455791-C-T

127945394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32455787-G-T

127945444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32455716-G-A

127945444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32455716-G-T

127945466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32455694-A-G

http://identifiers.org/hco/9/GRCh38#127945633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32455528-C-A

127945633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455528-C-T

127945838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455357-G-A

127945838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455357-G-T

127945892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455297-C-T

http://identifiers.org/hco/9/GRCh38#127945902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32455287-C-A

127945902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455287-C-G

127945902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32455287-C-T

127946530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32454436-G-A

127946695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32454293-C-G

127947959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32453876-T-C

127948004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32453830-G-T

127948124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453716-T-C

127948236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32453601-C-T

127948424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32453424-G-C

127948424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32453424-G-T

127948484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32453376-G-A

127948484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32453376-G-T

http://identifiers.org/hco/9/GRCh38#127948486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32453374-C-A

http://identifiers.org/hco/9/GRCh38#127948495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32453365-C-A

127948495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32453365-C-G

127949801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32450725-C-T

127949864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32450664-G-A

127950063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32450432-C-T

127950126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32450368-C-T

127950516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32450072-C-T

127950543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 32450045-G-A

127950543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 32450045-G-T

127950547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 32450041-G-A

http://identifiers.org/hco/9/GRCh38#127950557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32450032-C-A

127950557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32450032-C-T

http://identifiers.org/hco/9/GRCh38#127950586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32450004-C-A

127950586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32450004-C-T

127950728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32449875-C-T

127952055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32449200-G-T

127953666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32448270-C-T

127953763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32448185-T-C

127953766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32448183-A-G

http://identifiers.org/hco/9/GRCh38#127953786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32448173-C-A

127953938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32448027-G-A

http://identifiers.org/hco/9/GRCh38#127954074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32447936-C-A

http://identifiers.org/hco/9/GRCh38#127954075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32447935-C-A

127954075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32447935-C-T

127954076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32447934-A-T

127954152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32447857-G-A

127954152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32447857-G-T

127954154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32447855-G-C

127954270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32447787-T-C

127954377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32447694-G-A

127954512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32447609-G-A

127954919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32447397-G-A

127955104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32447246-G-C

127955175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32447150-G-A

127955194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32447131-G-A

127955452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32446917-G-A

127960635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32445766-T-C

127961114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32445281-G-A

127961114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32445281-G-T

127961242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32445198-G-A

http://identifiers.org/hco/9/GRCh38#127961271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32445179-C-A

127961528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32444847-G-T

127961984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32444452-C-T

127961992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32444444-C-T

127962050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32444384-T-G

127963057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32442713-G-A

127963376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32442413-C-T

http://identifiers.org/hco/9/GRCh38#127963584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32442217-C-A

127963689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32442110-A-G

127963735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32442062-C-T

http://identifiers.org/hco/9/GRCh38#127963750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32442049-A-C

127963750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32442049-A-G

http://identifiers.org/hco/9/GRCh38#127963759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32442040-C-A

127963759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32442040-C-T

127963795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32442003-G-A

127963795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32442003-G-T

http://identifiers.org/hco/9/GRCh38#127963816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32441986-C-A

http://identifiers.org/hco/9/GRCh38#127963924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32441914-C-A

127963924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32441914-C-T

127963987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32441864-C-G

127963987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32441864-C-T

127964297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32441161-C-G

127964297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32441161-C-T

127964581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32440931-A-G

127965285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32440440-T-G

127965288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32440436-C-T

127965291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32440433-T-C

127965358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32440371-C-T

http://identifiers.org/hco/9/GRCh38#127965647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32440108-C-A

127965647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32440108-C-T

127965994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32439750-C-G

127966166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32439584-A-G

http://identifiers.org/hco/9/GRCh38#127966699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32439159-A-C

127966875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32439004-G-A

http://identifiers.org/hco/9/GRCh38#127966895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32438984-C-A

127966950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32438950-T-C

127967077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32438825-G-A

127967377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32438766-C-T

127967765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32438433-G-A

127967861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32438339-C-T

http://identifiers.org/hco/9/GRCh38#127967935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32438271-C-A

127968274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32438102-T-C

127968548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32437865-T-A

127968907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32437499-A-G

127969182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32436415-G-A

127969182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32436415-G-T

127969431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32436167-T-G

http://identifiers.org/hco/9/GRCh38#127969577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#32436040-A-C

127969595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32436024-T-C

127969598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32436021-T-C

http://identifiers.org/hco/9/GRCh38#127969637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32435978-A-C

127969964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32435670-C-G

127970972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32433718-A-T

127971320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32433390-A-G

127971445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32433285-T-C

127972299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32432611-C-G

127972554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32432377-A-G

http://identifiers.org/hco/9/GRCh38#127972563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32432368-C-A

127972563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32432368-C-G

127972652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32432311-A-G

127972678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32432286-A-G

127972741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32432218-G-T

127973471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32431608-G-A

127973791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32431309-C-T

127973886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32431212-C-T

127973962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32431139-T-C

127974029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32431096-G-A

127974066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32431086-C-T

http://identifiers.org/hco/9/GRCh38#127974196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32430959-A-C

127974343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430816-T-G

127974406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430754-C-T

127974513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430656-G-C

127974648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430555-C-T

127974669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430533-G-T

127974936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430312-C-T

127975091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430177-G-T

127975092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430176-G-A

127975120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430128-C-T

127975157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430090-G-A

127975164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430083-C-G

127975164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430083-C-T

127975188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32430059-G-A

127975305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32429960-T-C

127975602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32429666-C-T

127975698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32429579-A-T

http://identifiers.org/hco/9/GRCh38#127975818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#32429506-A-C

127976198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32429135-C-T

127976283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32429051-G-C

127976977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32428462-T-C

127977196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32428262-T-G

127977381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32428072-C-T

127977408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32428045-G-A

127977408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32428045-G-C

127977562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32427905-C-T

127977618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32427854-C-T

127977891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32427629-T-C

127977947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32427573-T-C

127978320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32427241-C-T

127978372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32427189-C-T

127979414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32426801-C-T

127979585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32426630-G-A

127979738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32426481-T-A

127979738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32426481-T-C

127979738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32426481-T-G

127979855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32426376-T-C

127980067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32426167-A-G

127980278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32425912-G-A

127980278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32425912-G-C

127980278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32425912-G-T

127980280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32425910-C-G

127980280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32425910-C-T

127980480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32425773-G-A

127980480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31419
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 32425773-G-C