36014686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30007764-G-A

36014686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30007764-G-T

http://identifiers.org/hco/19/GRCh38#36014758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#30007692-C-A

36014758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30007692-C-T

36015134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30007288-G-T

http://identifiers.org/hco/19/GRCh38#36015255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#30007159-C-A

36015566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30006838-G-T

36015587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30006817-A-G

36015601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30006803-T-G

36015807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30006620-T-G

36015911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30006528-T-C

36015911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30006528-T-G

http://identifiers.org/hco/19/GRCh38#36016237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#30006204-C-A

36016237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30006204-C-T

36016245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30006200-G-A

36016327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30006106-T-A

36016327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30006106-T-C

36016340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30006093-G-A

36016340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30006093-G-T

36016357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30006065-T-A

36016429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30005900-C-T

36016555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30005747-C-T

36016639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30005668-C-T

36016756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30005406-A-G

http://identifiers.org/hco/19/GRCh38#36016864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#30005282-C-A

36016893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30005268-G-C

36016894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30005267-G-A

http://identifiers.org/hco/19/GRCh38#36017085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#30005067-C-A

36017090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30005062-G-A

36017091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30005061-G-T

36017140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30005014-C-T

36017303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30003481-C-T

36017424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30003361-C-G

36017553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30003258-G-A

36017553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30003258-G-T

36017600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30003208-G-A

36017600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30003208-G-C

36017600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30003208-G-T

36017629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30003179-G-A

http://identifiers.org/hco/19/GRCh38#36017823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#30002959-C-A

36017823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30002959-C-T

36018016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30002769-G-A

http://identifiers.org/hco/19/GRCh38#36018575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#30001977-C-A

36018575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30001977-C-G

36018741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30001827-G-A

36018773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30001795-G-C

36018773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30001795-G-T

36018776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30001792-A-G

36018777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30001791-C-G

http://identifiers.org/hco/19/GRCh38#36018874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#30001713-C-A

36018981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30001604-G-C

36018981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30001604-G-T

36019014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 30001571-G-T

http://identifiers.org/hco/19/GRCh38#36019027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#30001558-C-A

36019027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 30001558-C-T

36019127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30001447-T-C

36019127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30001447-T-G

36019139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30001435-C-T

36019152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30001424-G-A

http://identifiers.org/hco/19/GRCh38#36019296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#30001279-A-C

36019302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30001273-C-T

36019352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30001224-G-A

36019352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30001224-G-T

http://identifiers.org/hco/19/GRCh38#36019440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#30001143-C-A

36019440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30001143-C-G

36019440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30001143-C-T

http://identifiers.org/hco/19/GRCh38#36019470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#30001109-C-A

36021867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30000347-T-C

36021979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30000254-T-A

36022001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30000232-C-T

36022010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30000224-C-G

36022022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30000212-G-A

36022057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30000186-T-G

36023325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29999254-T-C

36023344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29999234-C-G

36023528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29999102-T-C

36023540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29999090-C-T

36023546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29999084-T-C

36023876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29998922-G-T

36024262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29998598-T-C

http://identifiers.org/hco/19/GRCh38#36024300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29998564-C-A

36024300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29998564-C-G

36024300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29998564-C-T

http://identifiers.org/hco/19/GRCh38#36024324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29998545-C-A

36024324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29998545-C-T

36024481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29998386-G-A

36024707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29998161-G-T

http://identifiers.org/hco/19/GRCh38#36024744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29998124-C-A

36024744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29998124-C-T

36024747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29998121-A-G

36024752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29998116-G-A

36024752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29998116-G-T

36024832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29998032-C-T

36024998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997909-A-G

36025049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997850-G-A

36025049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997850-G-C

36025922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997698-C-T

36025960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997658-G-A

36025960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997658-G-T

36025996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997618-T-G

36025997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997617-A-G

36025997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997617-A-T

36025998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997616-G-C

36025998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997616-G-T

36026008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997606-A-G

http://identifiers.org/hco/19/GRCh38#36026034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29997576-C-A

36026034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997576-C-T

36026093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997506-G-A

36026093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997506-G-T

36026099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997500-G-A

36026099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997500-G-C

36026099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997500-G-T

36026102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997497-G-T

36026274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997333-G-A

36026274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997333-G-T

http://identifiers.org/hco/19/GRCh38#36026314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29997280-C-A

36026314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997280-C-G

36026314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997280-C-T

http://identifiers.org/hco/19/GRCh38#36026358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29997233-C-A

36026358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997233-C-T

http://identifiers.org/hco/19/GRCh38#36026413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29997179-C-A

36026413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997179-C-G

36026413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997179-C-T

36026415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997177-G-A

36026415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997177-G-T

36026444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997160-T-A

36026444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997160-T-C

36026445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997159-G-A

36026445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997159-G-C

36026445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997159-G-T

36026527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997015-G-A

36026527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997015-G-T

36026540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29997002-C-T

http://identifiers.org/hco/19/GRCh38#36026542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29996982-C-A

http://identifiers.org/hco/19/GRCh38#36026558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29996967-C-A

http://identifiers.org/hco/19/GRCh38#36026568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29996957-C-A

36026568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996957-C-T

36026574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996951-T-C

36026591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29996934-G-A

36026591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29996934-G-C

36026591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29996934-G-T

36026594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29996931-C-G

36026615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29996910-C-T

36026639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29996886-T-C

36026657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29996868-G-A

36026732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29996793-G-A

36026732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29996793-G-T

36026735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29996790-G-A

36026735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29996790-G-T

36026749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 29996776-T-C

36026749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 29996776-T-G

36026759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996769-G-A

36026759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996769-G-T

36026802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996724-G-A

36026802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996724-G-T

36026805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996721-C-T

36026806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996720-G-A

36026806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996720-G-C

36026806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996720-G-T

36026818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996706-G-A

http://identifiers.org/hco/19/GRCh38#36026845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29996680-C-A

36026845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996680-C-T

36026922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996603-G-A

36026922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996603-G-T

36027344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996203-A-G

36027345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996202-G-C

http://identifiers.org/hco/19/GRCh38#36027411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29996136-C-A

36027411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996136-C-G

36027411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29996136-C-T

36028525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29994880-G-A

36028577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29994830-G-A

36028969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29994495-G-A

36029821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29994084-T-C

36030157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29993803-G-T

36030165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29993796-C-T

36030417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29993599-T-C

36030472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29993553-G-C

36030502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29993517-G-A

http://identifiers.org/hco/19/GRCh38#36030611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29993362-A-C

36030654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29993164-T-G

36031292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29992519-C-T

36031296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29992515-C-T

36031299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29992512-G-A

36031332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29992481-T-G

36031375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29992446-A-G

36031546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29992355-G-A

36031561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29992334-T-C

36031564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29992331-C-G

36031618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29992276-C-G

36031756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29992160-T-C

36031865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29992121-C-T

http://identifiers.org/hco/19/GRCh38#36032158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29991823-C-A

36032158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29991823-C-T

36032181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29991800-A-G

36032181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29991800-A-T

36032397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29991583-G-A

36032397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29991583-G-C

36032397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29991583-G-T

36032432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29991548-G-A

36032432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29991548-G-C

36032432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29991548-G-T

36032483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29991505-A-G

36032515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 29991468-T-C

36032549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29991433-G-T

36032742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29991247-G-A

36032742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29991247-G-T

http://identifiers.org/hco/19/GRCh38#36032793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#29991196-C-A