53062060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 5 prime UTR variant
orthologous variants: 107889281-C-T

http://identifiers.org/hco/1/GRCh38#53062067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107889274-C-A

53062249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107889113-G-A

53062249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107889113-G-T

53062253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107889109-A-G

53062253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 107889109-A-T

53062322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107889053-G-A

53062322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107889053-G-T

53062345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107889032-C-G

53062345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107889032-C-T

53062353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107889017-G-A

53062353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107889017-G-T

http://identifiers.org/hco/1/GRCh38#53062437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107888935-C-A

53062437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107888935-C-G

53062437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107888935-C-T

53062438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107888934-T-C

53062469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107888903-G-A

53062469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107888903-G-C

53062481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107888891-T-A

53062491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107888880-G-A

53062516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107888851-C-T

53062540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107888829-G-A

53062993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107888425-G-C

53063236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107888221-G-A

53063236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107888221-G-T

53063384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107888121-T-C

53063539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107888013-G-A

53063539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107888013-G-C

53063539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107888013-G-T

http://identifiers.org/hco/1/GRCh38#53063540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107888012-C-A

53063540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 107888012-C-T

http://identifiers.org/hco/1/GRCh38#53063644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107887916-C-A

53063644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107887916-C-T

53063687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107887881-T-A

53063779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107887799-T-C

53063818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107887761-T-C

53063930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107887637-A-G

53064027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107887561-C-T

53064043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107887545-C-T

53064276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107886864-G-A

53064437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107886752-A-G

53065574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107886575-G-A

http://identifiers.org/hco/1/GRCh38#53065647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107886528-C-A

53066470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107886156-T-C

53066686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885961-G-A

53066686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885961-G-T

53066767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885902-A-G

53066889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885781-G-A

53066889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885781-G-C

53066889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885781-G-T

http://identifiers.org/hco/1/GRCh38#53066975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107885700-C-A

53066975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885700-C-G

53067163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885594-G-A

53067163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885594-G-T

53067336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885431-C-T

53067347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885420-C-T

53067383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885398-G-A

53067388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885393-C-T

53067411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885374-A-G

53067430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885355-C-T

53067452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885333-T-C

53067486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885308-A-G

53067543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107885278-C-T

53069340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107884884-G-C

53069575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107884696-C-G

53069859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107884482-G-A

http://identifiers.org/hco/1/GRCh38#53069860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107884481-C-A

53069860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107884481-C-T

53069867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107884474-C-G

53069867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 107884474-C-T

http://identifiers.org/hco/1/GRCh38#53069935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107884409-C-A

53069935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 107884409-C-T

http://identifiers.org/hco/1/GRCh38#53070021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107884317-C-A

53070048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107884290-G-A

53070049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107884289-C-T

53070278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107884090-T-C

53070279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107884089-G-A

53070279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107884089-G-T

53070434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107883940-T-C

53070447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107883927-G-A

53070477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107883890-C-T

53070766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107883693-G-A

53070766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107883693-G-T

http://identifiers.org/hco/1/GRCh38#53070895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107883587-C-A

53070895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107883587-C-T

53070897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107883585-T-C

53070929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883552-G-C

53070929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883552-G-T

53070952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883531-G-T

http://identifiers.org/hco/1/GRCh38#53070991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107883488-C-A

http://identifiers.org/hco/1/GRCh38#53071002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107883474-C-A

53071050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883390-G-A

53071062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883372-G-A

53071065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883369-A-G

53071074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883360-T-C

53071108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883225-G-A

53071108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883225-G-C

53071108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883225-G-T

53071111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883222-G-A

53071111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883222-G-T

53071152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883112-G-A

53071157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883107-C-T

53071161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883103-A-G

53071161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883103-A-T

53071164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883100-G-A

53071164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107883100-G-T

53071337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107882969-T-C

53071403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107882946-T-G

53071474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107882884-G-T

http://identifiers.org/hco/1/GRCh38#53071491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107882862-C-A

53071491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107882862-C-T

http://identifiers.org/hco/1/GRCh38#53071505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107882840-C-A

http://identifiers.org/hco/1/GRCh38#53071526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107882813-C-A

53071526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107882813-C-T

http://identifiers.org/hco/1/GRCh38#53071559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107882780-C-A

http://identifiers.org/hco/1/GRCh38#53071574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107882765-C-A

53071574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107882765-C-T

53071622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107882717-T-A

53071640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107882703-C-T

http://identifiers.org/hco/1/GRCh38#53071688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107882669-C-A

53071688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107882669-C-G

53071688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107882669-C-T

http://identifiers.org/hco/1/GRCh38#53071720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107882648-C-A

53071720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107882648-C-T

53073582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107882459-G-A

53073688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107882364-C-G

53073784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107882265-C-G

53073784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107882265-C-T

53073886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107882140-G-A

53073887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107882139-T-C

53074133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107881913-G-A

53074133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107881913-G-C

53074143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107881903-G-A

53074749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107881353-C-G

53074781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107881290-T-A

53074781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107881290-T-C

53074781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107881290-T-G

53074811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107881258-G-A

53074811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107881258-G-C

53074811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107881258-G-T

53075588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107880847-C-T

53075866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107880603-C-T

53075990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107880477-T-A

53075990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107880477-T-C

53075990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107880477-T-G

53076011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107880442-G-T

53076013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107880440-G-A

53076013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107880440-G-T

http://identifiers.org/hco/1/GRCh38#53076102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107880326-C-A

53076102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107880326-C-T

53076122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107880276-A-G

53077073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879965-A-T

http://identifiers.org/hco/1/GRCh38#53077074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107879964-C-A

53077074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879964-C-G

53077074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879964-C-T

53077105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879933-G-A

53077105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879933-G-T

http://identifiers.org/hco/1/GRCh38#53077248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107879774-A-C

53077248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107879774-A-G

53077369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879654-G-A

53077409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879621-G-A

53077409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879621-G-C

53077413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879617-G-T

53077417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879613-G-A

53077423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879607-A-G

http://identifiers.org/hco/1/GRCh38#53077431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107879600-C-A

53077431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879600-C-T

http://identifiers.org/hco/1/GRCh38#53077432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107879599-C-A

53077432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879599-C-T

53077451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879578-G-A

53077451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879578-G-T

http://identifiers.org/hco/1/GRCh38#53077607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107879443-C-A

53077607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879443-C-G

http://identifiers.org/hco/1/GRCh38#53077617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107879433-C-A

53077617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879433-C-T

http://identifiers.org/hco/1/GRCh38#53077638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107879412-C-A

53077638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879412-C-T

http://identifiers.org/hco/1/GRCh38#53077669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107879386-C-A

53077669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879386-C-T

53077745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107879313-C-T

53077772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107879286-G-T

http://identifiers.org/hco/1/GRCh38#53077787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107879271-A-C

53077787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107879271-A-G

53077865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879201-A-G

http://identifiers.org/hco/1/GRCh38#53077909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107879145-C-A

53077936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879121-T-C

53077936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879121-T-G

53078323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107879048-T-C

53078369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107879002-C-T

53078513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107878858-C-T

53078522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107878849-C-G

53078522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107878849-C-T

53078618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107878753-G-A

53078780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107878591-G-A

http://identifiers.org/hco/1/GRCh38#53078840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107878531-A-C

53078840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107878531-A-G

53078840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107878531-A-T

53078906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 107878465-T-C

http://identifiers.org/hco/1/GRCh38#53078990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107878381-C-A

53078990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107878381-C-T

53079029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107878344-G-A

53079029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107878344-G-T

http://identifiers.org/hco/1/GRCh38#53079135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107878224-C-A

53079135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107878224-C-T

53079171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107878190-G-T

53079252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107878146-C-T

53079263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107878142-G-T

53079301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107878104-A-G

53080124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107876594-C-T

53080445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107876361-G-A

53080445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107876361-G-C

http://identifiers.org/hco/1/GRCh38#53080553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107876272-C-A

53080553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107876272-C-T

http://identifiers.org/hco/1/GRCh38#53080607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107876224-C-A

53080607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107876224-C-T

http://identifiers.org/hco/1/GRCh38#53080688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107876166-C-A

http://identifiers.org/hco/1/GRCh38#53080721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107876144-C-A

http://identifiers.org/hco/1/GRCh38#53080737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107876128-A-C

53080737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107876128-A-G

53080932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875938-A-G

http://identifiers.org/hco/1/GRCh38#53080976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107875852-C-A

53080976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875852-C-T

53080994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875839-A-T

53081015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875820-T-C

53081155-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875695-T-A

53081253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875598-C-T

53081256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875595-G-A

http://identifiers.org/hco/1/GRCh38#53081471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107875448-A-C

53081471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875448-A-G

53081741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875310-A-G

53081839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875226-G-T

http://identifiers.org/hco/1/GRCh38#53081892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107875176-C-A

53081892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875176-C-T

53081896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875172-T-C

53081939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875140-G-A

53081939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107875140-G-T

http://identifiers.org/hco/1/GRCh38#53081974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107875106-C-A

53082028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107875052-G-A

53082123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107874966-G-A

53082207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107874883-G-A

53082207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107874883-G-C

53082207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107874883-G-T

http://identifiers.org/hco/1/GRCh38#53082239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107874849-C-A

53082239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107874849-C-T

http://identifiers.org/hco/1/GRCh38#53082269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107874828-C-A

53082454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107874426-G-A

53082464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107874416-G-C

53082854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107874202-T-C

53082990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107874093-G-C

53082998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107874085-G-A

53083498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107873739-G-A

53083772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107873583-G-C

53083977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107873376-T-C

53084135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107873247-A-G

53084175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107873210-A-G

53084175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107873210-A-T

53084439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107872937-G-C

53084439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107872937-G-T

53084513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107872890-G-C

53084513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107872890-G-T

53084753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107872651-G-A

53084753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107872651-G-T

http://identifiers.org/hco/1/GRCh38#53084755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107872649-C-A

53084755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107872649-C-G

http://identifiers.org/hco/1/GRCh38#53084768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107872637-C-A

53084768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107872637-C-G

53084768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107872637-C-T

http://identifiers.org/hco/1/GRCh38#53084835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107872584-C-A

53084837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107872582-C-T

http://identifiers.org/hco/1/GRCh38#53084945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107872485-C-A

53084945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107872485-C-T

53085045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107872388-G-A

53085045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107872388-G-T

http://identifiers.org/hco/1/GRCh38#53085046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#107872387-C-A

53085046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107872387-C-T

53085129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107872307-G-A

53085137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 107872299-G-A

53085296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107872171-G-A

53085324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23174
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 107872150-A-G