77562601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152166695-G-A

77562601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152166695-G-T

http://identifiers.org/hco/1/GRCh38#77562697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152166593-C-A

77562935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152166434-G-A

77562959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152166410-C-G

77563012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152166360-A-G

http://identifiers.org/hco/1/GRCh38#77563059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152166312-A-C

http://identifiers.org/hco/1/GRCh38#77563216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152166157-C-A

77563364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152166042-A-G

77563454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152165979-T-A

77563533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152165916-G-C

77563690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152165787-T-C

77563698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152165780-T-C

77563709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152165769-G-C

77563786-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152165701-T-A

77564220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152165303-T-A

77564803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152164818-G-T

77564815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152164806-T-A

77564884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152164741-T-C

http://identifiers.org/hco/1/GRCh38#77564925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152164702-C-A

77565281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152164367-T-C

77565326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152164323-T-C

77565358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152164291-G-A

77565358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152164291-G-T

77565373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152164275-A-G

77565425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152164215-G-C

77565425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152164215-G-T

http://identifiers.org/hco/1/GRCh38#77565785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152163888-C-A

http://identifiers.org/hco/1/GRCh38#77565969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152163690-A-C

77566123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152163562-G-A

77566123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152163562-G-C

77566123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152163562-G-T

77566166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152163519-T-C

http://identifiers.org/hco/1/GRCh38#77566265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152163436-C-A

77566265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152163436-C-T

http://identifiers.org/hco/1/GRCh38#77566273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152163428-C-A

77566273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152163428-C-T

http://identifiers.org/hco/1/GRCh38#77566302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152163411-C-A

77566302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152163411-C-G

77566302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152163411-C-T

77566303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152163410-A-G

77566303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152163410-A-T

http://identifiers.org/hco/1/GRCh38#77566307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152163406-A-C

77566307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152163406-A-T

http://identifiers.org/hco/1/GRCh38#77566314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152163399-A-C

77566314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152163399-A-G

77566314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152163399-A-T

77566447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152163293-T-A

77566447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152163293-T-C

http://identifiers.org/hco/1/GRCh38#77568485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152161439-A-C

77568485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152161439-A-G

77568514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152161410-G-A

77568514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152161410-G-T

77568585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152161344-G-A

77568585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152161344-G-T

http://identifiers.org/hco/1/GRCh38#77568899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152160938-A-C

77572083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152159636-T-C

77573456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152158581-T-C

77575823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152158041-T-G

77575886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152157973-A-G

77575940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152157922-A-T

77575983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152157863-C-T

77575996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152157850-G-T

77576006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152157840-T-C

77576010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152157836-A-G

77576020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152157824-T-C

77576138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152157708-A-G

77578844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152156963-A-G

77578865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152156942-G-A

77578865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152156942-G-T

77579105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152156746-T-C

http://identifiers.org/hco/1/GRCh38#77579396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152156425-A-C

77579409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152156416-T-C

77579495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152156376-T-C

77579504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152156366-T-C

77579504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152156366-T-G

77579591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152156282-T-C

http://identifiers.org/hco/1/GRCh38#77579795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152156072-C-A

77580089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152155820-A-G

http://identifiers.org/hco/1/GRCh38#77580291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152155710-C-A

77580551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152155502-G-T

77580988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152155361-T-A

77580991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 152155358-T-C

77581082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152155268-C-G

77581082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152155268-C-T

77581086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152155264-G-C

77581086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152155264-G-T

77581127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152155235-T-A

77581127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152155235-T-C

77581127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152155235-T-G

http://identifiers.org/hco/1/GRCh38#77581377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152155087-A-C

77581585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152154933-G-A

http://identifiers.org/hco/1/GRCh38#77581757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152154782-A-C

77581757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152154782-A-G

77581767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152154772-A-G

77581783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152154756-C-T

77581818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 152154721-C-T

77581967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152154573-A-G

77583505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152153342-T-C

77583509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152153338-T-C

77583692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152153249-A-G

77583779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152153220-T-C

77583796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152153207-T-G

77584277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152152803-G-C

77584387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152152704-T-C

77585034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152152056-T-G

77585089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152152005-G-C

77585094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152152000-T-C

77585507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152151659-A-G

77585604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152151569-A-T

77585783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152151376-G-A

77585917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152151286-T-C

77586630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152151171-C-T

77587037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152150796-C-T

77587147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152150708-T-C

77587174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152150678-A-T

77589990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152149443-T-C

77589991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152149442-G-A

77619054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152142784-A-G

77619064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152142774-G-C

77619642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152142300-A-G

77619782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152142189-T-C

77619804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152142169-C-T

77623153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152139698-A-T

77626826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152138450-A-G

77627031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152138283-G-C

77627128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152138200-G-A

77627159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152138169-T-G

77628435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152137433-A-G

77628773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152137178-T-C

77628775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152137176-T-C

77628977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152136970-C-G

77628977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152136970-C-T

77629246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152136730-T-C

77631068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152135147-C-T

77631734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152134595-T-A

77631734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152134595-T-C

77631916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152134401-T-A

77631949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152134368-G-C

77632132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152134185-T-C

77632318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152133999-A-T

77632334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152133983-T-G

77633014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152133303-G-A

77633014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 152133303-G-C

77634569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152132205-C-T

77636138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152131022-T-C

77636141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152131019-T-C

77637001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152130438-C-T

http://identifiers.org/hco/1/GRCh38#77637092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152130315-A-C

77637754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152129979-T-C

77637754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152129979-T-G

77638112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152129629-G-A

77638258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152129492-T-A

77638744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152129070-G-A

http://identifiers.org/hco/1/GRCh38#77639431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152128424-C-A

77639431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152128424-C-T

77639545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152128310-A-G

77639553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152128302-A-G

77639553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 152128302-A-T

77639648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152128208-A-G

77639716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152128145-C-T

77639722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152128140-T-G

77639734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152128128-G-C

77639734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152128128-G-T

77639742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152128124-G-A

77639742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152128124-G-T

77640654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152127229-G-C

77641024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152126198-G-A

77641024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152126198-G-T

77641051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152126168-T-G

77641093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152126136-A-G

77641158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152126074-T-C

77641175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152126052-G-C

77641500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152125798-T-C

77641650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 152125655-T-C

77641779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152125544-T-C

http://identifiers.org/hco/1/GRCh38#77641796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152125521-C-A

77641828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152125488-G-C

77644546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152122473-G-A

77673322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152109150-C-T

77673838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152108636-C-T

http://identifiers.org/hco/1/GRCh38#77674071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152108373-C-A

77674309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152108205-C-G

77674309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152108205-C-T

77678971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152106259-A-G

77678980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152106250-T-C

77679072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152106162-A-G

http://identifiers.org/hco/1/GRCh38#77679817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152105508-A-C

77679924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152105417-A-G

77680674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152104162-T-A

77680895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152103802-T-A

77680895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152103802-T-C

http://identifiers.org/hco/1/GRCh38#77682354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#152102583-C-A

77682422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152102540-G-A

77682475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152102498-G-A

77682475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152102498-G-T

http://identifiers.org/hco/1/GRCh38#77682607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
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#152102373-C-A

77682607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 152102373-C-T

77682709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 152102266-C-T

77682725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152102250-A-G

http://identifiers.org/hco/1/GRCh38#77682785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#152102185-C-A

77682785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152102185-C-T

77682922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152102045-A-T

77682936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152102031-G-C

77682954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152102009-T-A

77682954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152102009-T-G

http://identifiers.org/hco/1/GRCh38#77682975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#152102005-C-A

77682975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152102005-C-G

http://identifiers.org/hco/1/GRCh38#77683073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#152101930-C-A

77683151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152101875-T-C

http://identifiers.org/hco/1/GRCh38#77683187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#152101847-C-A

77683199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152101835-C-T

77683223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152101811-G-A

77683223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152101811-G-C

77683223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 152101811-G-T

http://identifiers.org/hco/1/GRCh38#77683418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#152101633-C-A

77683418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24523
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 152101633-C-T