http://identifiers.org/hco/7/GRCh38#1470284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737051-C-A

1470366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3 prime UTR variant
orthologous variants: 139737137-A-G

1470367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3 prime UTR variant
orthologous variants: 139737138-T-C

1470371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3 prime UTR variant
orthologous variants: 139737142-G-A

1470371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3 prime UTR variant
orthologous variants: 139737142-G-T

http://identifiers.org/hco/7/GRCh38#1470373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737144-C-A

1470373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3 prime UTR variant
orthologous variants: 139737144-C-T

http://identifiers.org/hco/7/GRCh38#1470387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737156-C-A

1470387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3 prime UTR variant
orthologous variants: 139737156-C-T

1470430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3 prime UTR variant
orthologous variants: 139737196-T-C

1470430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3 prime UTR variant
orthologous variants: 139737196-T-G

1470449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3 prime UTR variant
orthologous variants: 139737217-T-C

http://identifiers.org/hco/7/GRCh38#1470519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737236-C-A

1470519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139737236-C-T

1470556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139737253-G-A

1470556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139737253-G-C

1470556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139737253-G-T

http://identifiers.org/hco/7/GRCh38#1470566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737263-C-A

1470566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139737263-C-T

http://identifiers.org/hco/7/GRCh38#1470569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737266-C-A

1470569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139737266-C-T

http://identifiers.org/hco/7/GRCh38#1470570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737267-C-A

1470570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 139737267-C-T

http://identifiers.org/hco/7/GRCh38#1470658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737354-C-A

1470658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139737354-C-G

1470658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139737354-C-T

1470669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139737365-G-A

1470669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139737365-G-T

http://identifiers.org/hco/7/GRCh38#1470800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737425-C-A

http://identifiers.org/hco/7/GRCh38#1470815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737438-C-A

1470815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139737438-C-G

1470815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139737438-C-T

http://identifiers.org/hco/7/GRCh38#1470821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737446-C-A

1470821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139737446-C-T

1470833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139737458-G-A

1470833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139737458-G-T

http://identifiers.org/hco/7/GRCh38#1470961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737580-A-C

1471060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139737657-G-C

1471110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139737670-A-G

http://identifiers.org/hco/7/GRCh38#1471130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737690-C-A

1471147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139737707-C-T

http://identifiers.org/hco/7/GRCh38#1471207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737767-C-A

1471207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139737767-C-T

1471234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139737794-G-A

1471234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139737794-G-C

1471234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139737794-G-T

http://identifiers.org/hco/7/GRCh38#1471368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139737893-C-A

1471368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139737893-C-T

1471409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139737915-C-T

1471604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139738009-G-A

1471604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139738009-G-C

1471660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139738061-C-T

1471721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139738120-G-A

1471721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139738120-G-T

1471756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139738175-G-A

1471756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 139738175-G-T

http://identifiers.org/hco/7/GRCh38#1471878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139738269-C-A

1471884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139738274-T-A

1471884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139738274-T-C

1471884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139738274-T-G

http://identifiers.org/hco/7/GRCh38#1471888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139738278-C-A

1471888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139738278-C-T

1471899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139738289-G-T

1471963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139738348-G-A

1471963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139738348-G-T

http://identifiers.org/hco/7/GRCh38#1472319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139738513-C-A

1472319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139738513-C-T

1472474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139738679-G-A

1472474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139738679-G-T

1472544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139738753-C-T

1472593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139738790-G-C

1472628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139738818-G-C

1472852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739004-G-A

1472905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739058-G-T

1472932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739093-G-A

1472932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739093-G-C

1472932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739093-G-T

http://identifiers.org/hco/7/GRCh38#1472933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139739094-C-A

1472933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739094-C-G

1472933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739094-C-T

1472940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739101-G-A

1472940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739101-G-T

1472943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739104-A-G

1472945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739106-G-C

1472945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739106-G-T

http://identifiers.org/hco/7/GRCh38#1472959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139739120-C-A

1472959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739120-C-G

1472959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739120-C-T

1472971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739132-G-A

1472971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739132-G-T

http://identifiers.org/hco/7/GRCh38#1472983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139739144-C-A

1472983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739144-C-T

1472990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739151-G-A

1472990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739151-G-T

http://identifiers.org/hco/7/GRCh38#1473033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139739179-C-A

1473033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139739179-C-G

1473118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139739262-G-A

1473118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139739262-G-T

1473262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739405-G-A

1473262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739405-G-T

1473292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739453-G-A

1473292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739453-G-T

http://identifiers.org/hco/7/GRCh38#1473293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139739454-A-C

1473293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739454-A-T

1473313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739483-G-A

1473313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739483-G-T

1473363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739549-G-A

1473363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739549-G-C

1473365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739551-G-C

http://identifiers.org/hco/7/GRCh38#1473510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139739772-C-A

1473510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739772-C-T

1473625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139739888-G-A

1473704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739977-A-G

1473708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139739981-C-T

http://identifiers.org/hco/7/GRCh38#1473791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139740187-C-A

1473791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139740187-C-G

1473791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139740187-C-T

http://identifiers.org/hco/7/GRCh38#1473792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139740188-C-A

1473946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139740434-G-A

1474031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139740501-G-A

1474031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139740501-G-C

1474031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139740501-G-T

1474048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139740539-G-A

1474048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139740539-G-T

1474114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139740598-G-A

1474114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139740598-G-C

1474114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139740598-G-T

1474126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139740607-G-A

1474126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139740607-G-T

1474127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139740608-G-A

1474127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139740608-G-T

1474222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 139740716-G-A

1474222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 139740716-G-C

1474222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 139740716-G-T

http://identifiers.org/hco/7/GRCh38#1474237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#139740731-C-A

1474237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 139740731-C-G

1474237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 139740731-C-T

1474267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 139740761-G-A

1474267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 139740761-G-C

1474267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 139740761-G-T

1474272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 139740766-G-A

1474272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 139740766-G-C

1474272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 139740766-G-T

1474637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139740914-G-T

1474640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139740917-T-C

1474681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139740918-A-T

1474718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139740945-G-A

1474718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139740945-G-C

1474718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139740945-G-T

1474758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139740985-A-G

1474826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139741053-T-C

1474830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139741057-T-C

http://identifiers.org/hco/7/GRCh38#1475969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139741653-A-C

1475969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139741653-A-T

1476052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 139741736-G-A

1476052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139741736-G-T

http://identifiers.org/hco/7/GRCh38#1476097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139741773-C-A

1476097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139741773-C-G

1476097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139741773-C-T

1476122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139741797-G-A

1476122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139741797-G-T

1476137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139741814-A-G

http://identifiers.org/hco/7/GRCh38#1476143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139741820-C-A

1476143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139741820-C-G

1476143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139741820-C-T

1476185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139741859-T-C

1476210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139741867-G-C

1476210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139741867-G-T

1476348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139742009-G-A

1476348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139742009-G-T

1476384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139742045-G-A

1476384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139742045-G-C

1476384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139742045-G-T

1476418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139742079-G-A

1476418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139742079-G-T

http://identifiers.org/hco/7/GRCh38#1476429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139742090-C-A

1476429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139742090-C-T

1476642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139742271-G-A

1476756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139742771-A-G

1476759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139742774-C-G

1476759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139742774-C-T

1476834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: stop gained
orthologous variants: 139742856-G-A

1476834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139742856-G-C

1476841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139742863-T-C

http://identifiers.org/hco/7/GRCh38#1476862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139742884-C-A

1476862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139742884-C-G

1476862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139742884-C-T

1476892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139742914-C-G

1476892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139742914-C-T

http://identifiers.org/hco/7/GRCh38#1476947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139742972-C-A

1476947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139742972-C-T

1476957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139742982-G-A

1476957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139742982-G-C

1476957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139742982-G-T

1476961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139742986-A-G

1477276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139743109-G-C

http://identifiers.org/hco/7/GRCh38#1477298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139743129-C-A

http://identifiers.org/hco/7/GRCh38#1477300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139743131-A-C

1477424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139743234-G-T

http://identifiers.org/hco/7/GRCh38#1477472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139743271-C-A

1477472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139743271-C-T

http://identifiers.org/hco/7/GRCh38#1477525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139743324-C-A

1477525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139743324-C-T

1477533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139743326-A-G

1477533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139743326-A-T

1477607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139743400-G-A

1477607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139743400-G-C

1477607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139743400-G-T

1477646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139743439-C-T

1477706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139743504-G-A

1477706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139743504-G-C

http://identifiers.org/hco/7/GRCh38#1477730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139743528-C-A

1477730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139743528-C-T

1477865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139743659-C-T

1477866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139743660-A-G

1478334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139743822-C-T

1478548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744023-A-G

1478553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744028-A-G

http://identifiers.org/hco/7/GRCh38#1478668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139744122-C-A

1478668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744122-C-G

1478668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744122-C-T

1478700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744150-G-A

1478700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744150-G-T

1478719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 139744178-T-C

1478719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 139744178-T-G

1478727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 139744186-A-G

1478902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744361-G-T

1478990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744444-C-T

1479061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744511-G-C

http://identifiers.org/hco/7/GRCh38#1479269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139744690-A-C

1479356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744780-G-T

http://identifiers.org/hco/7/GRCh38#1479360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139744784-C-A

1479360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744784-C-G

1479360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744784-C-T

1479407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744869-G-A

1479407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744869-G-C

1479407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744869-G-T

http://identifiers.org/hco/7/GRCh38#1479419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139744878-C-A

1479419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744878-C-G

1479419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139744878-C-T

1479460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139744921-G-A

1479460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: stop gained
orthologous variants: 139744921-G-T

1479478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139744939-A-G

http://identifiers.org/hco/7/GRCh38#1479495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139744956-C-A

1479495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139744956-C-T

1479571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139745032-G-A

1479571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139745032-G-C

1479571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139745032-G-T

http://identifiers.org/hco/7/GRCh38#1479605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139745066-C-A

1479605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139745066-C-T

1479670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139745131-G-A

1479670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139745131-G-T

http://identifiers.org/hco/7/GRCh38#1479737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139745169-C-A

1479737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745169-C-G

1479737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745169-C-T

1479753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745180-A-G

1479843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745260-C-T

http://identifiers.org/hco/7/GRCh38#1480236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139745454-C-A

1480236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745454-C-G

1480236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745454-C-T

http://identifiers.org/hco/7/GRCh38#1480245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139745463-C-A

1480245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745463-C-T

1480293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745478-A-G

1480293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745478-A-T

http://identifiers.org/hco/7/GRCh38#1480297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139745482-A-C

http://identifiers.org/hco/7/GRCh38#1480299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139745484-A-C

1480300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745485-T-A

1480300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745485-T-C

1480303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745488-A-G

1480360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139745545-C-T

1480362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139745547-G-A

1480362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139745547-G-C

1480434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139745619-T-G

1480481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745663-T-C

http://identifiers.org/hco/7/GRCh38#1480528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139745690-C-A

1480691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745790-G-A

1480691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745790-G-T

http://identifiers.org/hco/7/GRCh38#1480701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139745800-C-A

1480701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745800-C-T

1480714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139745807-C-G

1480866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139745869-G-T

1481042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746045-T-G

1481048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746051-G-A

1481048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746051-G-T

1481141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746238-G-A

1481141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746238-G-C

1481180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746277-G-A

1481180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746277-G-C

1481180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746277-G-T

1481183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746280-A-T

1481210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746304-T-C

http://identifiers.org/hco/7/GRCh38#1481243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139746334-C-A

1481243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746334-C-T

1481282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746363-G-T

1481322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746391-G-A

1481323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746392-C-T

1481376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139746443-G-A

1481451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 139746518-G-A

1481451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 139746518-G-C

1481451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 139746518-G-T

1481499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746566-A-G

1481547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746614-C-T

1481554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746621-G-A

1481554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139746621-G-T

1482571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139747063-A-G

1482577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139747069-G-A

1482577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139747069-G-T

http://identifiers.org/hco/7/GRCh38#1482685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139747177-C-A

1482685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139747177-C-G

1482685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139747177-C-T

1482723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 139747215-C-T

1483723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139747762-G-A

1483723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139747762-G-T

http://identifiers.org/hco/7/GRCh38#1483749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139747785-C-A

1483749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139747785-C-T

1483815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139747851-G-A

1483815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139747851-G-C

1483898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139747934-T-C

http://identifiers.org/hco/7/GRCh38#1483950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139747992-C-A

1483950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139747992-C-T

1484021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139748101-G-A

1484021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139748101-G-T

1484054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139748134-G-A

1484054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139748134-G-C

1484054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139748134-G-T

1484168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 139748248-G-A

http://identifiers.org/hco/7/GRCh38#1484211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139748287-C-A

1484211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139748287-C-T

1485131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139748402-C-T

1485138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139748409-G-A

1485138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139748409-G-C

1485138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139748409-G-T

1485167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139748438-G-A

1485167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139748438-G-T

1485264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139748539-G-A

1485264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139748539-G-T

http://identifiers.org/hco/7/GRCh38#1485265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139748540-C-A

1485265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139748540-C-T

1485287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139748560-C-T

http://identifiers.org/hco/7/GRCh38#1485377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139748650-C-A

1485377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139748650-C-G

1485377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139748650-C-T

1485440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139748713-G-A

http://identifiers.org/hco/7/GRCh38#1485449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139748722-C-A

1485449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139748722-C-T

1485510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139748792-G-A

1485510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139748792-G-C

1485510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139748792-G-T

http://identifiers.org/hco/7/GRCh38#1485533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139748815-C-A

1485533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139748815-C-T

http://identifiers.org/hco/7/GRCh38#1485534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139748816-C-A

1485534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139748816-C-T

http://identifiers.org/hco/7/GRCh38#1485557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139748830-C-A

1485576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139748850-T-C

1486782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139749917-G-A

1486823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139749947-G-C

1486823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139749947-G-T

1486914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139749974-G-A

1486914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139749974-G-T

1486997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139750058-A-G

1487015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139750076-G-A

1487015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 139750076-G-T

1487054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139750115-G-A

1487054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139750115-G-T

1487175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750248-C-T

1487186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750259-A-G

1487246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750340-G-A

1487246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750340-G-T

1487272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750374-G-A

1487272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750374-G-T

1487277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750379-T-C

1487302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750408-T-C

http://identifiers.org/hco/7/GRCh38#1487317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139750420-C-A

1487341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139750444-G-A

1487341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139750444-G-C

1487341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139750444-G-T

1487428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139750531-G-C

1487428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139750531-G-T

1487474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750576-C-T

http://identifiers.org/hco/7/GRCh38#1487484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139750586-C-A

1487484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750586-C-G

1487484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750586-C-T

http://identifiers.org/hco/7/GRCh38#1487510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139750622-C-A

1487510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750622-C-G

1487510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750622-C-T

1487514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750626-T-C

1487514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750626-T-G

http://identifiers.org/hco/7/GRCh38#1487515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139750627-C-A

1487515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750627-C-G

1487515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750627-C-T

http://identifiers.org/hco/7/GRCh38#1487518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139750630-C-A

1487518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750630-C-T

http://identifiers.org/hco/7/GRCh38#1487665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139750734-C-A

1487665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750734-C-G

1487665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139750734-C-T

http://identifiers.org/hco/7/GRCh38#1487687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139750754-C-A

1487768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139750807-C-T

1487858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139750897-G-T

1487928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139750967-G-A

1487980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751020-G-C

http://identifiers.org/hco/7/GRCh38#1487984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139751024-C-A

1488113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751109-G-C

1488126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751122-G-C

1488128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751124-G-A

1488143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751142-C-T

1488193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751186-C-T

1488569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751441-C-T

1488604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751469-C-T

1488605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751470-G-A

http://identifiers.org/hco/7/GRCh38#1488619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139751485-C-A

1488619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751485-C-T

1488686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751549-C-T

1488917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751705-G-T

1489017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751778-C-T

1489076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139751808-G-A

1489375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139752023-G-A

1489375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139752023-G-T

1489434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139752080-A-G

1489466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139752098-G-A

1489466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139752098-G-T

1489484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139752116-T-C

http://identifiers.org/hco/7/GRCh38#1489488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139752120-A-C

1489529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139752162-C-T

1489578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139752173-A-T

1489592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 139752186-G-A

1489592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 139752186-G-C

1489592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 139752186-G-T

1489613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139752207-G-A

1489613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139752207-G-C

1489613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139752207-G-T

http://identifiers.org/hco/7/GRCh38#1489713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139752307-C-A

1489713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139752307-C-T

1493135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139753281-G-T

1493160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139753304-C-G

1493160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139753304-C-T

http://identifiers.org/hco/7/GRCh38#1493773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139753495-C-A

1493773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139753495-C-G

1493773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139753495-C-T

1493845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139753567-G-A

1493845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139753567-G-T

http://identifiers.org/hco/7/GRCh38#1493915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139753637-C-A

1493915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 139753637-C-T

1493974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753662-G-A

1493974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753662-G-C

1493974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753662-G-T

http://identifiers.org/hco/7/GRCh38#1493979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139753667-C-A

1493979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753667-C-T

1494245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753832-G-A

1494330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753884-G-A

1494330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753884-G-T

1494337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753891-G-A

1494337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753891-G-C

1494337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753891-G-T

http://identifiers.org/hco/7/GRCh38#1494347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139753901-C-A

1494347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753901-C-G

1494347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753901-C-T

http://identifiers.org/hco/7/GRCh38#1494360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139753914-C-A

1494360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753914-C-T

1494377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753930-G-T

1494379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753933-G-A

1494379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753933-G-T

http://identifiers.org/hco/7/GRCh38#1494385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139753936-A-C

1494385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753936-A-G

1494385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753936-A-T

http://identifiers.org/hco/7/GRCh38#1494396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139753947-A-C

1494396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753947-A-G

1494396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753947-A-T

http://identifiers.org/hco/7/GRCh38#1494404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139753953-A-C

1494404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753953-A-G

1494404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753953-A-T

1494437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139753981-G-T

1494679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754068-G-T

1494743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754128-G-A

1494743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754128-G-T

1494785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754168-A-G

1494830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139754188-G-A

1494830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139754188-G-C

1494830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139754188-G-T

http://identifiers.org/hco/7/GRCh38#1494863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139754221-C-A

1494863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139754221-C-G

1494863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139754221-C-T

http://identifiers.org/hco/7/GRCh38#1494899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139754255-C-A

1494899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139754255-C-G

1494899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139754255-C-T

http://identifiers.org/hco/7/GRCh38#1494946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139754302-C-A

http://identifiers.org/hco/7/GRCh38#1494972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139754314-C-A

1494972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754314-C-G

1494972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754314-C-T

1494988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754330-A-G

http://identifiers.org/hco/7/GRCh38#1494990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139754332-C-A

1494990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754332-C-T

1495011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754347-G-A

1495011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754347-G-T

1495014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754350-G-A

1495014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754350-G-T

http://identifiers.org/hco/7/GRCh38#1495031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139754367-C-A

1495191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754463-G-A

1495203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754475-T-C

1495232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754485-G-A

http://identifiers.org/hco/7/GRCh38#1495266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139754505-C-A

1495266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754505-C-T

1495271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754510-G-C

1495271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754510-G-T

1495303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754528-T-A

1495303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754528-T-C

1495303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754528-T-G

1495304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754529-G-A

1495304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754529-G-T

1495311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754535-G-A

1495311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754535-G-C

1495351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754544-T-A

1495351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754544-T-G

1495352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754545-G-A

1495352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754545-G-C

1495352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754545-G-T

1495377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754562-G-A

1495377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754562-G-T

1495406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754589-A-G

1495418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754604-G-A

1495418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754604-G-T

1495419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754605-G-C

1495419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754605-G-T

http://identifiers.org/hco/7/GRCh38#1495424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139754610-C-A

1495424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754610-C-T

1495444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139754630-G-T

1495477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139754663-C-T

1495516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139754702-G-A

1495516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139754702-G-T

1495522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139754708-C-G

1495572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754759-T-C

http://identifiers.org/hco/7/GRCh38#1495581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139754768-C-A

1495581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754768-C-T

1495607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754791-T-A

1495607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754791-T-C

1495750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754858-C-T

1495760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754868-C-T

1495922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754978-C-T

1495939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139754987-C-T

1495976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755000-G-A

http://identifiers.org/hco/7/GRCh38#1495980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139755004-C-A

1495980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755004-C-G

1495982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755006-C-T

1495983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755007-G-C

http://identifiers.org/hco/7/GRCh38#1496016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139755009-C-A

1496016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755009-C-T

1496022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755015-G-A

1496022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755015-G-T

http://identifiers.org/hco/7/GRCh38#1496026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139755019-C-A

1496026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755019-C-T

1496028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755021-G-A

1496028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755021-G-T

1496076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755031-G-A

1496076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755031-G-T

http://identifiers.org/hco/7/GRCh38#1496117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139755032-C-A

1496117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139755032-C-T

1496305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755174-C-T

1496310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755179-G-A

1496506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755264-A-T

1496602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755314-G-A

1496602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755314-G-C

1496604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755316-G-A

http://identifiers.org/hco/7/GRCh38#1496786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139755491-C-A

1496786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755491-C-T

http://identifiers.org/hco/7/GRCh38#1497004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139755706-C-A

1497004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755706-C-G

1497004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755706-C-T

1497005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755707-T-C

1497085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755768-G-A

1497085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755768-G-T

http://identifiers.org/hco/7/GRCh38#1497096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139755779-C-A

1497096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755779-C-G

1497096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755779-C-T

1497103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139755786-T-C

1497255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139755935-C-G

1497255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139755935-C-T

http://identifiers.org/hco/7/GRCh38#1497261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139755941-C-A

1497261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139755941-C-T

1497363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756053-T-C

1497363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756053-T-G

1497371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756060-G-A

1497371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756060-G-T

1497400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756154-C-G

1497400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756154-C-T

1497437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756198-G-A

1497484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756243-G-A

1497531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756291-G-A

1497531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756291-G-C

1497630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756380-A-G

1497739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756442-G-A

1497964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756505-A-G

1498126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756586-G-C

1498205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756621-G-A

1498205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756621-G-C

1498205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756621-G-T

1498387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756768-G-C

http://identifiers.org/hco/7/GRCh38#1498418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139756811-C-A

1498418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139756811-C-T

1498423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139756816-G-A

1498514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139756907-G-A

http://identifiers.org/hco/7/GRCh38#1498538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139756931-C-A

1498538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139756931-C-G

1498538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139756931-C-T

1498556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 139756967-G-A

1498556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 139756967-G-T

1498567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756979-G-T

1498573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756985-A-T

http://identifiers.org/hco/7/GRCh38#1498585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139756995-C-A

1498585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139756995-C-T

1498633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757002-C-T

1498634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757003-C-T

1498637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757006-G-A

1498637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757006-G-C

1498637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757006-G-T

http://identifiers.org/hco/7/GRCh38#1498660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139757018-A-C

1498660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757018-A-G

1498660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757018-A-T

http://identifiers.org/hco/7/GRCh38#1498702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139757040-C-A

1498702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757040-C-G

1498702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757040-C-T

1498760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757098-G-A

1498760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139757098-G-C

1498760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757098-G-T

1498772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757110-G-A

1498772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139757110-G-C

1498796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757134-G-A

1498796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139757134-G-C

1498796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139757134-G-T

http://identifiers.org/hco/7/GRCh38#1498799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139757137-C-A

1498799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757137-C-G

1498799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757137-C-T

1498820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757158-G-A

1498820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757158-G-C

1498820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757158-G-T

1498838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757176-G-A

1498838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757176-G-C

1498838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757176-G-T

http://identifiers.org/hco/7/GRCh38#1498891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139757230-C-A

1498891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757230-C-T

1498894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757233-G-A

1498930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757256-G-A

1498930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757256-G-C

1498930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757256-G-T

http://identifiers.org/hco/7/GRCh38#1498937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139757263-C-A

1498937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757263-C-G

1498937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757263-C-T

http://identifiers.org/hco/7/GRCh38#1498941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139757267-C-A

1498941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757267-C-T

http://identifiers.org/hco/7/GRCh38#1499011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139757328-C-A

1499011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757328-C-T

1499062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757379-G-A

1499062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757379-G-C

http://identifiers.org/hco/7/GRCh38#1499152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139757469-C-A

1499152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: 139757469-C-G

1499152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757469-C-T

1499174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757491-A-G

http://identifiers.org/hco/7/GRCh38#1499219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139757539-C-A

1499219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757539-C-T

1499231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757551-G-A

http://identifiers.org/hco/7/GRCh38#1499314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139757630-C-A

1499314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757630-C-T

1499323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757639-G-A

1499402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757732-G-A

1499402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757732-G-C

1499402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139757732-G-T

http://identifiers.org/hco/7/GRCh38#1499507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139757806-C-A

1499507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757806-C-T

1499522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139757821-G-A

1499588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139757887-G-A

http://identifiers.org/hco/7/GRCh38#1499707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139757978-C-A

1499707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139757978-C-T

1499714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139757983-T-C

1499714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139757983-T-G

1499715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139757984-G-C

1499715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139757984-G-T

http://identifiers.org/hco/7/GRCh38#1499770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139758017-C-A

1499770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139758017-C-T

http://identifiers.org/hco/7/GRCh38#1499862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139758091-C-A

1499862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139758091-C-T

1499926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139758153-G-A

1499962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139758189-G-A

1499962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 139758189-G-T

1499992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139758219-G-A

1499992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139758219-G-C

1500035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139758269-C-G

1500035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139758269-C-T

1500078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139758304-G-A

http://identifiers.org/hco/7/GRCh38#1500158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139758343-C-A

1500158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139758343-C-T

1500163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 139758348-C-T

http://identifiers.org/hco/7/GRCh38#1500278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139758461-C-A

1500311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139758494-A-G

http://identifiers.org/hco/7/GRCh38#1500344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139758527-A-C

1500344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 139758527-A-G

1500456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 139758657-A-G

http://identifiers.org/hco/7/GRCh38#1500462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139758663-C-A

1502110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759247-A-G

1502114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759251-A-G

1502120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759257-C-T

1502129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759266-C-T

1502146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759283-C-G

1502146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759283-C-T

1502167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759309-G-A

1502167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759309-G-C

1502235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759367-T-C

1502800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759943-G-T

http://identifiers.org/hco/7/GRCh38#1502801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139759944-C-A

1502839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759980-G-A

1502839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759980-G-C

1502839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139759980-G-T

1502908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139760050-T-C

1503025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139760167-G-A

1503034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139760176-G-A

1503034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139760176-G-C

http://identifiers.org/hco/7/GRCh38#1503055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139760197-C-A

1503055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139760197-C-T

http://identifiers.org/hco/7/GRCh38#1503124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139760266-C-A

1503124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139760266-C-G

1503124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: synonymous variant
orthologous variants: 139760266-C-T

1503270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760372-T-C

1503293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760385-T-A

http://identifiers.org/hco/7/GRCh38#1503329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139760421-C-A

1503329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760421-C-T

1503338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760429-G-A

1503370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760440-G-T

1503385-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760455-C-G

1503385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760455-C-T

http://identifiers.org/hco/7/GRCh38#1503453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139760517-C-A

1503563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760628-G-A

1503563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760628-G-T

1503762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760916-T-C

1503770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760941-G-A

1503770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760941-G-T

http://identifiers.org/hco/7/GRCh38#1503773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139760944-C-A

1503773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139760944-C-T

1503824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139761010-T-A

1503827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139761013-G-A

1503827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139761013-G-T

http://identifiers.org/hco/7/GRCh38#1503854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#139761036-C-A

1503854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139761036-C-T

1503997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5 prime UTR variant
orthologous variants: 139761181-G-A

1503997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5 prime UTR variant
orthologous variants: 139761181-G-C

1503997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5 prime UTR variant
orthologous variants: 139761181-G-T

1504039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139761205-T-C

1504039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron variant
orthologous variants: 139761205-T-G

1504181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139761294-C-T

1504217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139761321-G-A

1504220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139761324-G-A

1504307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139761367-G-A

1504307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: intron_variant, undefined
orthologous variants: 139761367-G-T

http://identifiers.org/hco/7/GRCh38#1504329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#139761382-C-A

1504329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139761382-C-T

1504333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139761386-T-A

1504333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139761386-T-C

1504333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139761386-T-G

http://identifiers.org/hco/7/GRCh38#1504358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#139761404-A-C

1504358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139761404-A-G

1504358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139761404-A-T

1504362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139761408-G-A

1504362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139761408-G-C

1504362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139761408-G-T

http://identifiers.org/hco/7/GRCh38#1504365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#139761411-C-A

1504365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139761411-C-G

1504365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24555
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 139761411-C-T