62701372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105251678-G-T

62701469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105251757-G-T

62701590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105251862-G-T

62701620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105251886-G-A

62701620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105251886-G-T

62701827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105252077-G-A

62701827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105252077-G-T

62701830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105252080-C-T

62702017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105252227-T-C

62702241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105252384-C-G

62702292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105252428-G-T

62702335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105252470-G-A

62702341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105252476-G-A

62702742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105252534-A-G

62702815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105252607-C-T

62703168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105252915-C-T

62703205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105252951-A-G

62703285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105253030-G-A

62703285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105253030-G-T

62703399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105253147-A-G

http://identifiers.org/hco/17/GRCh38#62703416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105253164-C-A

62703416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105253164-C-T

62703503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105253258-T-G

http://identifiers.org/hco/17/GRCh38#62703546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105253315-C-A

62703546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105253315-C-T

http://identifiers.org/hco/17/GRCh38#62703668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105253412-C-A

62703759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105253495-G-A

62703938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105253843-G-C

http://identifiers.org/hco/17/GRCh38#62704061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105253950-C-A

62704061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105253950-C-T

62704079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105253967-G-A

62704162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105254023-G-A

http://identifiers.org/hco/17/GRCh38#62704218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105254064-C-A

62704218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105254064-C-G

62704218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105254064-C-T

62704344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105254174-G-A

62704346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105254176-G-A

62704371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105254209-G-C

62704823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105254677-T-C

http://identifiers.org/hco/17/GRCh38#62704858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105254711-C-A

http://identifiers.org/hco/17/GRCh38#62704970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105254815-A-C

62704970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105254815-A-G

62705123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105254938-G-A

62705123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105254938-G-C

62705123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105254938-G-T

62705130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105254945-T-G

62705223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105255058-G-C

62705807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105255584-C-T

62706220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105256006-G-A

62706220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105256006-G-T

62706262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105256048-C-T

62706271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105256058-A-G

http://identifiers.org/hco/17/GRCh38#62706310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105256097-C-A

62706310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105256097-C-G

62706310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105256097-C-T

62706493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105256295-G-A

62706493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105256295-G-T

http://identifiers.org/hco/17/GRCh38#62706614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105256389-C-A

62706614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105256389-C-T

http://identifiers.org/hco/17/GRCh38#62707331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105257181-A-C

62707377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105257219-C-T

62707418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105257260-G-A

62707418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105257260-G-T

62707419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105257261-C-T

62707472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105257311-G-T

62707632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105257452-G-A

62707632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105257452-G-C

62707632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105257452-G-T

http://identifiers.org/hco/17/GRCh38#62707688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105257486-C-A

62707690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105257488-G-T

http://identifiers.org/hco/17/GRCh38#62707702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105257500-C-A

62707702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105257500-C-G

62707702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105257500-C-T

62708767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105258114-A-G

62708787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105258134-C-T

62708982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105258308-A-G

62709085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105259171-G-T

62709939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105260562-T-A

62710097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105260707-C-T

62710320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105260916-T-C

62710540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105261192-T-C

62710961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105262422-T-C

62711087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105262545-G-T

62711181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105262640-A-G

62711385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105262841-T-C

62711394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105262850-T-A

62711404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105262861-G-T

http://identifiers.org/hco/17/GRCh38#62711493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105262954-C-A

62711527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105262986-C-T

http://identifiers.org/hco/17/GRCh38#62711608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105263063-C-A

62712349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105264782-A-T

62712672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105265106-G-A

62712672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105265106-G-T

62713067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105265248-C-T

62713115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105265273-A-G

62713531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105265657-C-T

62714069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105266249-G-A

62714069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105266249-G-T

62714088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105266268-G-A

62714182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105266367-C-G

62714204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105266392-C-T

62714255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105266424-C-G

62714255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105266424-C-T

62714256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105266425-G-A

62714256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105266425-G-T

62714283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105266450-G-A

62714289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105266456-T-A

62714289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105266456-T-G

62714290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105266457-G-T

62714359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105266530-T-C

62714368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105266539-C-T

62716532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267250-G-A

62716617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267332-C-G

62716647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105267363-T-C

62721913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272490-C-G

62722001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272582-G-A

62722051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272618-G-A

62722051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272618-G-C

62722473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272966-G-A

62722473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105272966-G-T

62722613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105273110-G-T

http://identifiers.org/hco/17/GRCh38#62722632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105273199-C-A

62722632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105273199-C-T

62722686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105273253-T-A

62722691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105273260-G-A

62722691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105273260-G-T

62722946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105273523-A-G

62724223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105275392-C-T

62724570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105275925-T-C

62724972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 105276277-G-T

http://identifiers.org/hco/17/GRCh38#62725126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105276433-C-A

62725126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105276433-C-T

62725145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105276452-G-A

62725145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105276452-G-T

62725193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105276501-A-G

62734799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278689-T-C

62734951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105278843-T-C

62735134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105279347-A-G

http://identifiers.org/hco/17/GRCh38#62735310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105279522-C-A

62735321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105279533-A-G

62735355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105279567-A-T

http://identifiers.org/hco/17/GRCh38#62735503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105279710-C-A

http://identifiers.org/hco/17/GRCh38#62735636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105279853-C-A

62735659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105279873-T-A

62735659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105279873-T-C

62735780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105280242-A-G

http://identifiers.org/hco/17/GRCh38#62735842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105280307-C-A

62735842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105280307-C-T

62735960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105280439-G-A

62735960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105280439-G-T

http://identifiers.org/hco/17/GRCh38#62736028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105280504-C-A

62736190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105280660-T-C

62736338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, synonymous_variant
orthologous variants: 105280781-G-A

62736553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105280996-A-G

62736553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105280996-A-T

62736570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105281013-G-A

62736621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105281061-T-C

62736763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105281188-C-G

62736898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105281317-T-C

62737102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105281515-G-A

62737434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105281859-G-A

62737434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105281859-G-T

http://identifiers.org/hco/17/GRCh38#62737481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105281914-A-C

http://identifiers.org/hco/17/GRCh38#62737493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105281930-C-A

62737493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105281930-C-T

62737544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105281995-T-C

http://identifiers.org/hco/17/GRCh38#62737562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105282068-C-A

62737562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105282068-C-T

62737610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105282116-C-T

http://identifiers.org/hco/17/GRCh38#62737672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105282145-C-A

62737672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105282145-C-G

62737672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105282145-C-T

62737718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105282184-A-T

http://identifiers.org/hco/17/GRCh38#62737723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105282189-C-A

http://identifiers.org/hco/17/GRCh38#62737775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105282241-C-A

http://identifiers.org/hco/17/GRCh38#62737876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105282341-C-A

62738024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105282606-A-G

62738163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283077-A-G

62738329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283245-T-C

62738356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283272-T-C

62738437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283347-T-C

62738508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283414-C-T

http://identifiers.org/hco/17/GRCh38#62738565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105283458-C-A

62738565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283458-C-T

62738686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283570-G-A

62738738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105283622-T-G

62739694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105284039-T-C

http://identifiers.org/hco/17/GRCh38#62739891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105284258-C-A

62739891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105284258-C-T

62739921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105284286-G-A

62740014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105284356-C-T

62740248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105284460-C-T

62740250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105284461-A-G

62740422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105284630-T-C

http://identifiers.org/hco/17/GRCh38#62740602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105284798-C-A

62743242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105287004-A-G

62743242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105287004-A-T

62743252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105287014-C-T

62743487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105287145-C-T

62743929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105287444-C-T

http://identifiers.org/hco/17/GRCh38#62744153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105287589-C-A

62744153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105287589-C-T

http://identifiers.org/hco/17/GRCh38#62744246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105287657-C-A

62744246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105287657-C-T

62744404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105287803-A-T

62744435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105287834-C-G

62744458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105287857-T-C

http://identifiers.org/hco/17/GRCh38#62744491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105287890-C-A

62744491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105287890-C-T

http://identifiers.org/hco/17/GRCh38#62744605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105288024-C-A

62744605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105288024-C-T

62744653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105288068-G-A

62744653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105288068-G-C

62744666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105288081-T-A

62744666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105288081-T-C

62744764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105288178-T-G

62745436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105288499-G-T

62745602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105288636-G-T

62745964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105288941-G-T

62746062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105289040-T-C

62746098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105289076-T-C

62746260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105289219-T-C

62746774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105289897-A-G

http://identifiers.org/hco/17/GRCh38#62746779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105289902-C-A

62746779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105289902-C-T

62746799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105289922-C-T

http://identifiers.org/hco/17/GRCh38#62746800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105289923-C-A

62746835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105289958-G-A

62746835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105289958-G-T

62746846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105289963-G-A

62746846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105289963-G-T

62746873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105289990-G-T

62746915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105290021-C-T

62747045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105290136-T-C

62747119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105290199-T-G

62747332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105290370-C-T

62747727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105290972-T-C

62748980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105291538-T-G

62749025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105291581-G-C

http://identifiers.org/hco/17/GRCh38#62749230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105291757-A-C

62749230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105291757-A-G

62749230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105291757-A-T

62749568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105292082-C-T

62749753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105292270-A-G

62749829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105292349-C-T

62750068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105292580-T-C

62750333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105292826-T-C

62750333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105292826-T-G

62750464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105292954-A-G

http://identifiers.org/hco/17/GRCh38#62750465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105292955-C-A

62750562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105293052-G-A

62750562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105293052-G-T

62750648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105293179-G-A

http://identifiers.org/hco/17/GRCh38#62751266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105293836-C-A

62751266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105293836-C-T

62754489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105294713-A-G

62754686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105294896-G-A

62754757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105294983-G-A

62754762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105294988-T-G

62754778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105295004-G-C

62754778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105295004-G-T

62754835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105295063-C-T

62755084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105295307-T-C

62755466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105295724-C-T

62755583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105295823-C-G

62755738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105295981-C-T

62756577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105296408-G-A

62756607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105296438-T-C

62756836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105296674-G-A

62756836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105296674-G-T

62757444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105297220-C-T

62757810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105298076-C-T

62758396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105298389-C-G

62758437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105298402-G-A

62758734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105298702-G-A

62758780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105298747-G-C

62758796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105298763-A-T

62759070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105299047-G-C

62759097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105299074-T-G

62759112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105299089-C-T

62759806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105299440-T-C

62759913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105299547-T-C

62760001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105299635-A-G

62760080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105299696-G-T

62760094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105299720-G-T

http://identifiers.org/hco/17/GRCh38#62760106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105299732-C-A

http://identifiers.org/hco/17/GRCh38#62760128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105299754-C-A

62760128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105299754-C-T

62760176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105299798-G-A

http://identifiers.org/hco/17/GRCh38#62760180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105299802-C-A

62760209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105299827-T-C

62760444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105300086-G-A

62761175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105300767-A-G

62761177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105300769-C-T

62761347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105300938-A-G

62762142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105301359-G-A

62762437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105301656-G-C

62762582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105301758-T-C

62762583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105301759-G-A

62762930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105301867-A-G

62762966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105301898-C-T

62763117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105302097-A-G

62763402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105302351-C-T

62763661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105302606-G-T

http://identifiers.org/hco/17/GRCh38#62763826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105302766-A-C

http://identifiers.org/hco/17/GRCh38#62764322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105303323-C-A

62764322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105303323-C-T

62766598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105303699-T-C

62766662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105303744-G-A

62766847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105303896-A-G

62767000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105304086-G-T

62767272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105304377-C-T

http://identifiers.org/hco/17/GRCh38#62767298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105304396-A-C

62767333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105304432-T-C

62767357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105304456-G-A

62775413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105313221-C-T

62775419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105313227-C-T

62775484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105313290-G-T

62776403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105313923-G-A

62776435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105313955-A-G

62776698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105314203-A-G

62777133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105314475-C-T

62777154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105314497-G-A

62777999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105314557-G-C

62778254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105314761-G-C

62778677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105315114-T-C

62778677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105315114-T-G

62778740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105315188-T-A

62778740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105315188-T-C

62778904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105315354-G-T

62779699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105316203-A-G

62780638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105317597-T-C

62780816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105317989-A-G

62781129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105318246-G-A

62781191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105318306-G-A

http://identifiers.org/hco/17/GRCh38#62781276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105318400-C-A

62782030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105325528-T-C

62782087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105325582-C-T

62782303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105325791-A-G

62782707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105325865-C-T

http://identifiers.org/hco/17/GRCh38#62782822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105325986-C-A

62782822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105325986-C-G

62782822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105325986-C-T

62782826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105325989-A-G

62783165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105326284-G-C

62783165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105326284-G-T

62786609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105326576-G-A

62787120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105327104-T-C

62787429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105327409-A-G

62787972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105328822-T-A

62788002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105328844-T-C

62788141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105328976-C-G

62788405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105329585-T-A

62788405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105329585-T-C

62788407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105329587-A-G

62788407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105329587-A-T

62788409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105329589-A-G

62788409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105329589-A-T

62788487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105329652-G-A

62788658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105329839-T-C

62788710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105329890-G-A

62788710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105329890-G-T

http://identifiers.org/hco/17/GRCh38#62788715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105329895-C-A

62788715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105329895-C-T

62789111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105329975-T-A

62789111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105329975-T-C

62790474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105332457-C-T

62790732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105332707-C-T

http://identifiers.org/hco/17/GRCh38#62790832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105332818-C-A

62790832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105332818-C-T

62791343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105333671-A-G

62791630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105333955-C-G

62791630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105333955-C-T

62791842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105334141-G-A

62791842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105334141-G-C

62791842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105334141-G-T

62791847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105334146-G-T

62791975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105334271-G-A

http://identifiers.org/hco/17/GRCh38#62792131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105334374-A-C

62792175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105334407-T-G

62792244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105334468-C-T

62792395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105334608-T-C

62794287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105334678-T-C

62794357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105334733-T-C

62794470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105334829-T-A

http://identifiers.org/hco/17/GRCh38#62794512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105334869-C-A

62794555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105334915-A-G

62794871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105335573-T-C

62795129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105335920-C-T

62795130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105335921-G-A

62795130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105335921-G-T

62795336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105336147-A-G

62795371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105336277-A-G

62795548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105336452-T-C

62795646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105336548-G-C

62795774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105336689-G-A

62795776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105336691-G-T

62795948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105336885-T-C

62796130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105337058-G-A

http://identifiers.org/hco/17/GRCh38#62796162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105337100-C-A

62796162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105337100-C-T

62797538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105337692-A-G

62797582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105337744-C-G

62797590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105337752-C-G

62797736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105337943-C-G

62797736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105337943-C-T

62797875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105338085-G-T

62797949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105338157-G-A

62797949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105338157-G-T

62797968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105338174-C-T

62798002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105338209-G-C

62798616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105338631-G-A

62798848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105338984-T-C

62798898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105339032-A-T

62798908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105339042-A-G

62799130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105339213-T-C

62799993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105340092-T-C

62800238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105340359-G-A

62800253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105340374-C-T

62800258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105340379-C-G

62800342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105340459-C-G

62800684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105340805-T-A

62800684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105340805-T-G

62800941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105341070-G-A

62800967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105341096-A-G

62801179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105341386-G-A

62801306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105341521-A-T

62801500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105341777-A-G

62801500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105341777-A-T

62801547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105341817-G-A

62801547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105341817-G-T

62801550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105341820-A-G

http://identifiers.org/hco/17/GRCh38#62801551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105341821-A-C

62801560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105341830-G-T

62801609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105341869-G-T

62801616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105341876-C-G

62801641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105341897-A-G

62801809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105342104-A-G

http://identifiers.org/hco/17/GRCh38#62801834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105342129-C-A

62801834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105342129-C-G

62801834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105342129-C-T

62801836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105342131-T-G

http://identifiers.org/hco/17/GRCh38#62801885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105342181-C-A

62801885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105342181-C-T

62801907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105342191-T-C

62802018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105342303-T-C

62802035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105342326-G-A

62804200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105343729-G-A

http://identifiers.org/hco/17/GRCh38#62804383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105343911-A-C

62804429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105343953-C-T

62804509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105344023-C-T

62804784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105344318-G-A

62804784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105344318-G-T

http://identifiers.org/hco/17/GRCh38#62804803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105344337-C-A

62804803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105344337-C-T

62804914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105344426-G-A

http://identifiers.org/hco/17/GRCh38#62804949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105344444-A-C

62804949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105344444-A-G

62804955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105344451-G-A

62804955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105344451-G-T

62805063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105344617-A-G

http://identifiers.org/hco/17/GRCh38#62805071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105344672-C-A

62805071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105344672-C-T

62805356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105345184-G-C

http://identifiers.org/hco/17/GRCh38#62805365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105345193-C-A

62805432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105345258-A-G

62805595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105345423-C-T

62805968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105345492-C-G

62806347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105345867-A-G

62806376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105345903-T-C

62806385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105345912-C-T

62806386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105345913-G-A

62806386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105345913-G-C

62806386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105345913-G-T

62806395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105345920-T-C

62806460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105345984-T-C

62806777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105346271-G-A

62806777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105346271-G-T

62806827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105346358-C-T

62806925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105346487-T-G

62808017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105347254-A-G

62808067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105347290-G-A

62808067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105347290-G-C

62808068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105347291-G-A

http://identifiers.org/hco/17/GRCh38#62808179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#105347395-C-A

62808179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105347395-C-T

62808181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105347397-G-A

62808181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105347397-G-T

http://identifiers.org/hco/17/GRCh38#62808254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#105347471-C-A

62808271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105347488-G-A

62808271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26655
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105347488-G-T