161104734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69505679-T-C

http://identifiers.org/hco/3/GRCh38#161104809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69505764-C-A

161104809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69505764-C-T

http://identifiers.org/hco/3/GRCh38#161105034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69505939-C-A

161105034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69505939-C-G

161105035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69505940-G-A

161105035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69505940-G-C

161105035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69505940-G-T

161105093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69506012-T-C

161105194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69506097-A-G

161105277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69506168-G-A

http://identifiers.org/hco/3/GRCh38#161105290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69506181-C-A

161105290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69506181-C-T

http://identifiers.org/hco/3/GRCh38#161105336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69506234-C-A

161105336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69506234-C-T

161105358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69506256-G-A

161106737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69509300-C-G

161106758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69509321-G-A

161107241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69510982-T-G

161107609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69511398-T-C

161107762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69511547-T-C

161107794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69511579-G-C

161107812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69511598-A-G

161107813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69511599-A-G

161107963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69511930-G-T

161107988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69511955-G-A

161108351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69512318-A-G

161108420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69512380-G-A

http://identifiers.org/hco/3/GRCh38#161162734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69575114-C-A

161162757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69575137-A-G

161162835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69575208-G-C

http://identifiers.org/hco/3/GRCh38#161163037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69575346-C-A

161163048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69575356-C-T

161163134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69575446-G-A

161163176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69575490-G-A

http://identifiers.org/hco/3/GRCh38#161167514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69576448-C-A

161167711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69576641-C-T

161167735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69576666-C-T

161167813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69576723-C-T

161167975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69577034-C-T

161168038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69577240-A-G

161168076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69577312-G-A

http://identifiers.org/hco/3/GRCh38#161168126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69577353-A-C

161168255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69577482-G-A

http://identifiers.org/hco/3/GRCh38#161168592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69578260-A-C

161168774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69578407-T-C

161168793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69578423-G-A

161175758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69588185-G-A

161175758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69588185-G-T

161176247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69589337-C-T

161176350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69589441-T-C

161176938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69592477-T-C

161177082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69592627-G-A

161177438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69593050-T-C

161177459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69593065-C-T

161177460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69593066-G-A

161178134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69594741-C-G

161178134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69594741-C-T

161198601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69607263-C-T

161202757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69610552-C-T

161202797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69610587-G-A

161202797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69610587-G-T

http://identifiers.org/hco/3/GRCh38#161206207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69612295-A-C

161206275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69612354-G-A

161206635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69612687-T-C

161207482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69615790-G-A

161207482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69615790-G-T

161208109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69616113-T-C

161208307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69616325-G-T

161208362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69616379-C-T

161208407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69616424-T-G

161208673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69616705-G-A

161208848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69616880-T-G

161208969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69617079-G-T

161209000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69617121-T-G

161209068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69617360-C-T

161209084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69617379-G-C

161209400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69617703-A-G

161209401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69617704-A-G

161209439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69617791-G-A

http://identifiers.org/hco/3/GRCh38#161209844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69618321-C-A

161209849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69618326-T-G

161209909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69618410-G-T

161210271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69618819-G-C

161210431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69618962-C-T

http://identifiers.org/hco/3/GRCh38#161210663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69623961-A-C

161210750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69624049-G-C

161210750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69624049-G-T

161221147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629181-G-C

161221167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629197-T-C

http://identifiers.org/hco/3/GRCh38#161221176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69629205-C-A

161221176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629205-C-G

161221176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629205-C-T

161221177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629206-G-T

http://identifiers.org/hco/3/GRCh38#161221193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69629223-C-A

161221194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629224-A-G

http://identifiers.org/hco/3/GRCh38#161221214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69629247-C-A

http://identifiers.org/hco/3/GRCh38#161221227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69629261-C-A

161221227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629261-C-T

161221253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629303-T-C

http://identifiers.org/hco/3/GRCh38#161221255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69629305-C-A

161221255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629305-C-T

161221260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629311-T-C

161221266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629317-G-C

161221266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629317-G-T

http://identifiers.org/hco/3/GRCh38#161221268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69629319-C-A

161221282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629333-G-A

161221282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 69629333-G-T

http://identifiers.org/hco/3/GRCh38#161221291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69629342-C-A

161221291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69629342-C-T

161221293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 69629344-T-C

http://identifiers.org/hco/3/GRCh38#161221353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69629407-C-A

161221353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69629407-C-T

161221365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69629419-T-A

161221372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69629426-G-T

161221405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69629452-G-A

161221441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629490-G-C

161221441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629490-G-T

http://identifiers.org/hco/3/GRCh38#161221444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69629493-C-A

161221444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629493-C-T

161221467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629513-G-T

161221479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629522-C-G

161221479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629522-C-T

161221494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629537-G-A

161221541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629600-G-A

161221541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629600-G-C

161221541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629600-G-T

http://identifiers.org/hco/3/GRCh38#161221558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69629614-C-A

161221558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629614-C-G

161221558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629614-C-T

http://identifiers.org/hco/3/GRCh38#161221574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69629628-C-A

161221574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69629628-C-T

161222017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69629759-G-A

161222017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 69629759-G-T

161224364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69631038-C-G

161224521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69631164-T-G

161224531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69631171-A-T

161224552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69631182-C-T

http://identifiers.org/hco/3/GRCh38#161224786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69631413-A-C

161224786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69631413-A-G

161224805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69631462-A-T

161224808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69631465-T-A

161225056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69631716-A-G

161225112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69631772-T-A

161225130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69631790-T-C

161225130-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69631790-T-G

161225154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69631814-G-T

161225180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69631838-T-A

161225621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69632024-G-A

161225629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69632032-A-G

161225631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69632034-A-G

161225970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69632294-A-G

http://identifiers.org/hco/3/GRCh38#161226008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69632332-C-A

161226008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69632332-C-T

161226833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69632926-G-A

161227155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69633605-G-A

161227155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69633605-G-C

161227155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69633605-G-T

161227188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69633636-T-A

161227215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69633664-G-A

161227215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69633664-G-T

161227216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69633665-T-C

161227424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69633862-T-G

161227439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69633883-T-A

161231764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69634380-G-T

161231825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69634425-G-C

161232082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69634660-C-G

161232187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69634787-G-C

161232266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69634875-G-C

161232551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69635092-A-G

161232613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69635155-C-T

161232787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69635269-C-T

161232959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69635639-T-A

161232996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69635688-A-G

http://identifiers.org/hco/3/GRCh38#161233079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69635773-C-A

161233079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69635773-C-T

161233274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69635937-G-A

161233274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69635937-G-T

161233277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69635940-G-A

161233277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69635940-G-T

161233299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69636574-A-T

161233321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69636599-A-G

161233330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69636608-T-C

http://identifiers.org/hco/3/GRCh38#161233335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69636613-C-A

161233335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69636613-C-T

http://identifiers.org/hco/3/GRCh38#161233370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69636646-C-A

161233370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69636646-C-G

161233370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69636646-C-T

161233410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69636682-A-T

http://identifiers.org/hco/3/GRCh38#161233504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69636775-C-A

161233504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69636775-C-T

161233547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69636818-G-A

161233547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69636818-G-T

http://identifiers.org/hco/3/GRCh38#161233599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69636870-C-A

161233599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69636870-C-T

161233885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69637069-G-T

161234025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69637199-G-A

http://identifiers.org/hco/3/GRCh38#161234039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69637213-A-C

161234552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69637578-C-T

http://identifiers.org/hco/3/GRCh38#161234560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69637586-A-C

161234575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69637602-T-G

161234590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69637617-A-G

161234592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69637619-T-A

161234593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69637620-T-A

161234601-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69637622-T-A

161234601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69637622-T-G

161234682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69637693-A-G

161234691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69637702-A-G

161234765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69637776-G-A

161234807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69637818-A-G

161234852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69637863-A-G

161234852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69637863-A-T

161234912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69637923-A-G

161234963-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69638740-T-A

161235055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69638835-T-C

http://identifiers.org/hco/3/GRCh38#161235063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69638847-C-A

http://identifiers.org/hco/3/GRCh38#161235097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69638877-A-C

161235097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69638877-A-T

161235114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 69638890-T-C

161235130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69638906-T-C

161235272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69639048-G-A

161235272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69639048-G-T

161237871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69642143-C-T

161238028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69642301-A-G

http://identifiers.org/hco/3/GRCh38#161238248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69642507-C-A

161238248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69642507-C-T

http://identifiers.org/hco/3/GRCh38#161238265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69642524-C-A

161238265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69642524-C-T

http://identifiers.org/hco/3/GRCh38#161238271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69642530-C-A

161238271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69642530-C-T

http://identifiers.org/hco/3/GRCh38#161238274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69642533-C-A

http://identifiers.org/hco/3/GRCh38#161238292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69642555-C-A

161238292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69642555-C-G

161238292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69642555-C-T

http://identifiers.org/hco/3/GRCh38#161238341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69642662-C-A

161238397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69642731-G-A

161238397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69642731-G-T

161238418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69642752-A-G

161238445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69642779-G-A

161238633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69643250-G-T

161238712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69643309-T-A

161238727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 69643323-T-C

161238760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69643356-A-G

161238840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69643437-T-C

161238840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69643437-T-G

http://identifiers.org/hco/3/GRCh38#161238878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69643473-A-C

161238878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69643473-A-G

161238878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69643473-A-T

161238947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69643535-T-C

161238947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69643535-T-G

http://identifiers.org/hco/3/GRCh38#161238971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69643559-C-A

161238971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69643559-C-T

161239041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69643620-G-A

161240188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69646227-A-G

161240208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69646243-A-G

161240208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69646243-A-T

http://identifiers.org/hco/3/GRCh38#161240378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69646772-A-C

161240389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69646787-G-T

161240950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647155-T-C

161240982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647185-A-G

161240988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647191-G-T

161241001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647206-T-C

161241109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69647316-G-A

161241109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69647316-G-C

161241205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647425-A-G

161241205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647425-A-T

161241239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647691-T-A

161241258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647736-T-C

161241311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647777-G-A

161241311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647777-G-T

161241402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647858-A-G

161241415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647872-A-T

161241420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647877-C-T

http://identifiers.org/hco/3/GRCh38#161241461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69647910-C-A

161241469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647919-G-A

161241469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69647919-G-T

161241757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69648176-A-G

161241762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69648181-C-T

161242014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69648410-C-G

161242014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69648410-C-T

161242186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69648569-G-A

161242360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69648727-A-T

http://identifiers.org/hco/3/GRCh38#161242387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69648746-C-A

161242387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69648746-C-T

161242694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69649018-T-C

161242704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69649028-T-C

161242731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69649062-T-A

161242731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69649062-T-C

http://identifiers.org/hco/3/GRCh38#161242759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69649090-C-A

161242759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69649090-C-T

161246025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69650575-G-A

161246252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69650796-A-G

161246338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 69650851-T-A

161246338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 69650851-T-C

161246371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69650884-T-A

161246371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69650884-T-C

161246475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69650991-G-A

161246475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69650991-G-T

http://identifiers.org/hco/3/GRCh38#161246528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69651041-C-A

161246688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69651539-G-C

161247166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69652455-G-C

161247166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69652455-G-T

161247309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69652597-C-G

161247309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69652597-C-T

http://identifiers.org/hco/3/GRCh38#161247349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69652640-C-A

http://identifiers.org/hco/3/GRCh38#161247358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69652649-C-A

161247381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69652657-A-G

161248140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69652682-C-T

161248319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69652849-A-G

161248560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653035-A-G

161248593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653062-A-G

161248684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653153-T-C

161248766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653236-C-T

161248780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653247-T-A

161249060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653703-A-G

161249136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653773-T-G

161249182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653818-T-G

161249291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653903-G-A

161249319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653930-G-A

161249332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69653943-T-C

http://identifiers.org/hco/3/GRCh38#161249436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69654043-C-A

161249436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69654043-C-T

161249568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 69654175-T-C

161249588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69654195-T-C

161249634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69654238-G-C

161249671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69654275-A-G

http://identifiers.org/hco/3/GRCh38#161249706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69654309-C-A

http://identifiers.org/hco/3/GRCh38#161249754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69654369-C-A

161249996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69654496-G-A

http://identifiers.org/hco/3/GRCh38#161250322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/3/GRCm39#69655697-C-A

161250322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: synonymous variant
orthologous variants: 69655697-C-T

http://identifiers.org/hco/3/GRCh38#161250425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69655815-C-A

161250425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69655815-C-G

http://identifiers.org/hco/3/GRCh38#161250448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69655838-C-A

161250448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69655838-C-G

161250473-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69655858-T-A

161250473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69655858-T-C

161250482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69655867-A-G

161250658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69656009-G-C

161250665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69656016-T-A

161250940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656269-G-A

161250975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656301-T-C

http://identifiers.org/hco/3/GRCh38#161250991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69656317-C-A

161251058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656379-A-G

161251135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656455-G-A

161251135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656455-G-T

161251144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656464-A-G

http://identifiers.org/hco/3/GRCh38#161251145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69656465-C-A

161251145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656465-C-T

161251146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656466-A-G

161251181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656503-G-A

161251181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656503-G-C

161251181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656503-G-T

161251199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656520-A-G

161251204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656525-A-G

161251204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656525-A-T

161251245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656564-G-A

161251245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656564-G-C

161251245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69656564-G-T

http://identifiers.org/hco/3/GRCh38#161251330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69656655-A-C

http://identifiers.org/hco/3/GRCh38#161251473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69656886-C-A

161251822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69657211-A-G

161251927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69657307-C-G

161251927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69657307-C-T

161252160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69657498-G-C

161252663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69657767-T-A

161252663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69657767-T-G

161252746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69657838-A-G

161252756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron variant
orthologous variants: 69657848-T-A

161252763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 69657855-T-C

http://identifiers.org/hco/3/GRCh38#161252775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69657866-C-A

161252775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: missense variant
orthologous variants: 69657866-C-T

161252903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657900-A-G

161253032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657920-G-A

161253143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657926-G-A

161253143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657926-G-T

161253150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657933-T-C

161253150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657933-T-G

161253177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657959-G-A

161253177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657959-G-C

161253177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657959-G-T

http://identifiers.org/hco/3/GRCh38#161253185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69657967-C-A

161253185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657967-C-G

161253185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657967-C-T

http://identifiers.org/hco/3/GRCh38#161253206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69657988-A-C

161253206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657988-A-G

161253215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69657997-C-T

http://identifiers.org/hco/3/GRCh38#161253316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69658093-C-A

http://identifiers.org/hco/3/GRCh38#161253341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#69658133-C-A

161253447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69658244-A-G

161253451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69658246-A-G

161253456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69658251-A-G

161253517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24250
most severe consequence: 3 prime UTR variant
orthologous variants: 69658365-T-C