http://identifiers.org/hco/1/GRCh38#180913010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155120159-C-A

180913010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5 prime UTR variant
orthologous variants: 155120159-C-T

http://identifiers.org/hco/1/GRCh38#180913085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155120120-C-A

180913085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5 prime UTR variant
orthologous variants: 155120120-C-G

180913085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5 prime UTR variant
orthologous variants: 155120120-C-T

180913152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5 prime UTR variant
orthologous variants: 155120062-G-A

180913152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5 prime UTR variant
orthologous variants: 155120062-G-T

http://identifiers.org/hco/1/GRCh38#180913183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155120031-C-A

180913183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155120031-C-G

180913183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155120031-C-T

http://identifiers.org/hco/1/GRCh38#180913195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155120019-C-A

180913195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155120019-C-G

180913195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 155120019-C-T

180913406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155119865-G-A

180913406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155119865-G-T

180914168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155119112-C-G

180914419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155118900-G-A

http://identifiers.org/hco/1/GRCh38#180916023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155118188-C-A

180916023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155118188-C-T

180916119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155118099-T-C

180916187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: synonymous variant
orthologous variants: 155118040-C-T

http://identifiers.org/hco/1/GRCh38#180916280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155117950-C-A

180916305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense variant
orthologous variants: 155117925-C-G

180916305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: stop gained
orthologous variants: 155117925-C-T

180916362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense variant
orthologous variants: 155117868-G-T

180916585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense variant
orthologous variants: 155117663-C-T

180916655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: synonymous variant
orthologous variants: 155117608-C-T

180916682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: synonymous variant
orthologous variants: 155117581-A-G

180916698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense variant
orthologous variants: 155117565-A-G

180916845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense variant
orthologous variants: 155117421-G-A

180916845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense variant
orthologous variants: 155117421-G-T

180916852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense variant
orthologous variants: 155117414-C-T

180916875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense variant
orthologous variants: 155117391-T-A

180917088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense variant
orthologous variants: 155117181-A-G

180917484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155116856-T-C

180917506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155116836-G-A

180917521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155116821-G-T

180917705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155116714-A-G

180917854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense variant
orthologous variants: 155116540-G-A

180917854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense variant
orthologous variants: 155116540-G-T

180917981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155116437-T-A

180918006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155116404-G-A

180918006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155116404-G-C

180918006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155116404-G-T

180918046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155116363-A-G

180918123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155116312-T-C

180918285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155116176-G-A

180918298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155116163-C-G

180918681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155115813-T-C

180918734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, undefined
orthologous variants: 155115764-G-A

http://identifiers.org/hco/1/GRCh38#180918774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155115742-C-A

180919476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155115263-C-T

180919551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155115195-G-C

180920269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155114429-G-A

180920390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155114339-C-G

180920437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155114288-C-T

180920520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155114253-C-G

180920854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155113956-C-T

180921556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155113728-C-T

180921661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155113608-G-A

180923888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, undefined
orthologous variants: 155112906-C-T

180923895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155112899-C-T

180923995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155112799-C-T

180924744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155112247-T-C

180924760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155112234-C-G

180924760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155112234-C-T

180925004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155112003-T-A

180925004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155112003-T-G

180925695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, undefined
orthologous variants: 155111403-G-A

180925780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155111330-C-G

180925781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155111329-T-C

180925877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155111238-A-G

180926042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155111087-G-A

180926042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155111087-G-C

180926050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155111079-C-T

180926878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155109770-C-G

180926888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155109760-C-T

180927067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155109620-T-C

180927108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155109579-C-G

180927363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155109365-C-T

180927374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155109354-A-G

180927645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155109097-C-T

180927887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155108868-A-G

180928008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155108734-T-C

180928008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155108734-T-G

180928083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155108660-T-C

180928118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155108627-A-T

http://identifiers.org/hco/1/GRCh38#180928151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155108595-C-A

180928151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155108595-C-T

180928167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155108591-C-T

http://identifiers.org/hco/1/GRCh38#180928177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155108581-C-A

180928302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155108458-G-A

180928313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155108447-G-A

180928313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155108447-G-T

http://identifiers.org/hco/1/GRCh38#180928314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155108446-C-A

180928314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155108446-C-T

http://identifiers.org/hco/1/GRCh38#180928411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155108350-C-A

180928411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 155108350-C-T

180928502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 155108261-C-T

180928628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155108139-G-A

180928628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155108139-G-T

http://identifiers.org/hco/1/GRCh38#180928702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#155107935-C-A

180928702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, undefined
orthologous variants: 155107935-C-T

http://identifiers.org/hco/1/GRCh38#180928703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#155107934-A-C

180928814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155107827-G-A

180928814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155107827-G-T

180928976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155107662-G-C

http://identifiers.org/hco/1/GRCh38#180929439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155106966-A-C

180929753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155106674-G-A

180929852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155106572-G-A

180929852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155106572-G-C

180930349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155106309-G-A

180930644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155106114-C-T

180931206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155105564-A-G

180931427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155105415-G-C

180931473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155105375-A-G

180931473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155105375-A-T

180931539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155105315-T-C

180931582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155105281-A-G

180931931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155104627-G-A

180933432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155103707-A-G

180933767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155103490-C-G

180933947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155103340-C-T

180934864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155102465-G-C

180934915-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155102410-T-G

http://identifiers.org/hco/1/GRCh38#180934976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155102342-C-A

180934976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155102342-C-G

180934976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155102342-C-T

http://identifiers.org/hco/1/GRCh38#180935069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155102235-C-A

180935141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155102166-A-G

http://identifiers.org/hco/1/GRCh38#180935142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155102165-C-A

180935142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 155102165-C-T

http://identifiers.org/hco/1/GRCh38#180935159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155102148-C-A

180935159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155102148-C-T

http://identifiers.org/hco/1/GRCh38#180935173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155102134-C-A

http://identifiers.org/hco/1/GRCh38#180935230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155102077-C-A

180935230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155102077-C-G

180935230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155102077-C-T

http://identifiers.org/hco/1/GRCh38#180935302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155102005-C-A

180935302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155102005-C-G

180935302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 155102005-C-T

180935372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101935-T-A

180935372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101935-T-C

180935430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 155101892-G-A

180935430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 155101892-G-T

http://identifiers.org/hco/1/GRCh38#180935434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155101888-C-A

180935434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, stop_gained
orthologous variants: 155101888-C-T

http://identifiers.org/hco/1/GRCh38#180935446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155101876-C-A

180935446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101876-C-G

180935446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101876-C-T

http://identifiers.org/hco/1/GRCh38#180935497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155101825-C-A

180935497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101825-C-G

180935497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101825-C-T

http://identifiers.org/hco/1/GRCh38#180935640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155101661-C-A

180935640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101661-C-G

180935640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 155101661-C-T

180935693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 155101626-G-A

180935693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 155101626-G-T

180935740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 155101570-G-A

180935761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101549-T-C

180935806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 155101507-G-A

180935818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 155101495-T-A

180935819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 155101494-G-A

180935945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 155101365-G-A

180935945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 155101365-G-T

180935973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 155101337-G-A

180935996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 155101314-C-T

http://identifiers.org/hco/1/GRCh38#180936055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155101252-C-A

180936055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101252-C-T

http://identifiers.org/hco/1/GRCh38#180936115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155101198-C-A

180936115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101198-C-G

180936115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101198-C-T

180936227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101083-T-G

180936302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155101008-C-G

180936354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 155100962-A-G

180936365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155100951-C-T

180936556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155100769-A-G

180936579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant
orthologous variants: 155100746-G-T

180936680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155100646-T-C

180936923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155100455-G-C

http://identifiers.org/hco/1/GRCh38#180936947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155100428-C-A

180936947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155100428-C-T

180937141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155100270-T-C

180937187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155100228-T-C

180937703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099924-A-G

180937969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099705-C-T

180938033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099640-C-G

180938063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099604-G-A

180938090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099575-A-G

http://identifiers.org/hco/1/GRCh38#180938270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155099447-C-A

180938270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099447-C-G

180938270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099447-C-T

180938360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099348-G-A

180938435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099295-T-A

180938435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099295-T-C

http://identifiers.org/hco/1/GRCh38#180938526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155099204-A-C

180938532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099198-G-A

180938532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099198-G-C

180938532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155099198-G-T

180938614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155099116-A-G

180938701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155099029-G-T

http://identifiers.org/hco/1/GRCh38#180938805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155098942-A-C

180938805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155098942-A-G

180938805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155098942-A-T

180938820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155098928-G-A

180938820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155098928-G-C

180938820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155098928-G-T

180939318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155098226-A-G

180939322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155098222-C-T

180939765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155097900-C-T

180940906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097433-T-G

180940954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097397-T-C

180940954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097397-T-G

http://identifiers.org/hco/1/GRCh38#180940958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155097393-C-A

180940958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097393-C-G

180940958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097393-C-T

http://identifiers.org/hco/1/GRCh38#180940976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155097378-C-A

180940976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097378-C-G

180940976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097378-C-T

http://identifiers.org/hco/1/GRCh38#180940987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155097367-C-A

180940987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097367-C-G

180940987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097367-C-T

http://identifiers.org/hco/1/GRCh38#180940989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155097365-C-A

180940989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097365-C-G

180940989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097365-C-T

http://identifiers.org/hco/1/GRCh38#180940990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155097364-C-A

180940990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097364-C-G

180940990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155097364-C-T

180941056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155097320-G-A

180941116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155097260-G-A

http://identifiers.org/hco/1/GRCh38#180941177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155097199-C-A

180941189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 155097187-G-A

180941325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155097037-G-A

180941325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155097037-G-C

180941325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155097037-G-T

http://identifiers.org/hco/1/GRCh38#180941326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155097036-C-A

180941326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155097036-C-T

180941328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155097034-G-A

http://identifiers.org/hco/1/GRCh38#180941428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155096963-A-C

180941428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155096963-A-G

180941428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron variant
orthologous variants: 155096963-A-T

180944287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155094237-T-C

180944399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155094121-C-G

180944399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 155094121-C-T

180944657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093880-G-A

180944662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093875-G-A

180944662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093875-G-T

http://identifiers.org/hco/1/GRCh38#180944664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155093874-C-A

180944664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093874-C-T

180944741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093800-T-A

180944741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093800-T-C

180944741-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093800-T-G

180944743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093798-G-A

180944743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093798-G-T

180944768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093775-T-A

180944768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093775-T-C

180944768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093775-T-G

180944800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093743-T-C

180944800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093743-T-G

http://identifiers.org/hco/1/GRCh38#180944883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155093681-C-A

180944883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093681-C-G

180944883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093681-C-T

http://identifiers.org/hco/1/GRCh38#180944934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155093657-A-C

180944934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093657-A-G

http://identifiers.org/hco/1/GRCh38#180945125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155093479-C-A

180945125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093479-C-T

http://identifiers.org/hco/1/GRCh38#180945146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155093459-C-A

180945146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093459-C-T

http://identifiers.org/hco/1/GRCh38#180945198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155093409-C-A

180945198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093409-C-G

180945198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093409-C-T

180945246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093361-A-G

180945273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093338-G-T

180945379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 155093234-C-T

180945385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 155093228-G-A

180945457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155093156-G-A

180945457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155093156-G-C

180945463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155093150-T-C

180945463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155093150-T-G

http://identifiers.org/hco/1/GRCh38#180945475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155093138-C-A

180945475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155093138-C-T

180945565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 155093083-G-C

180945671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093008-G-A

180945678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155093004-T-C

http://identifiers.org/hco/1/GRCh38#180945795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155092943-C-A

180945795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 155092943-C-G

180946496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155092589-C-T

180946560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155092527-G-A

180946560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155092527-G-T

http://identifiers.org/hco/1/GRCh38#180946656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155092469-C-A

180946679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155092452-T-C

180946687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155092444-T-C

http://identifiers.org/hco/1/GRCh38#180948169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155091288-C-A

180948169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155091288-C-T

180948525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090966-G-T

http://identifiers.org/hco/1/GRCh38#180948581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155090911-C-A

180948581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090911-C-T

180948623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090869-T-C

http://identifiers.org/hco/1/GRCh38#180948626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155090866-C-A

180948681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090809-A-G

180948849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090638-G-C

180948849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090638-G-T

180948858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090629-T-C

180949075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090460-G-T

http://identifiers.org/hco/1/GRCh38#180949289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155090262-C-A

180949340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090228-G-A

180949346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090222-G-C

180949346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090222-G-T

http://identifiers.org/hco/1/GRCh38#180949434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155090142-C-A

180949434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090142-C-G

180949434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090142-C-T

180949450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090134-C-T

180949480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090113-T-A

180949483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090110-T-A

http://identifiers.org/hco/1/GRCh38#180949528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155090071-C-A

180949528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090071-C-T

180949554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090047-A-G

180949594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090027-G-A

180949594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090027-G-T

http://identifiers.org/hco/1/GRCh38#180949599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155090021-C-A

180949599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155090021-C-T

180949636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155089970-T-C

180949653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155089951-G-A

180949654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155089950-G-A

180949654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155089950-G-C

180949654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155089950-G-T

http://identifiers.org/hco/1/GRCh38#180949683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155089925-C-A

180949773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089857-G-T

http://identifiers.org/hco/1/GRCh38#180949888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155089754-C-A

180949888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089754-C-T

180950007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089671-A-G

180950007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089671-A-T

180950098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089576-A-G

http://identifiers.org/hco/1/GRCh38#180950128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155089547-A-C

180950128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089547-A-G

180950128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089547-A-T

180950129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089546-G-A

180950129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089546-G-T

180950139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089536-A-G

180950149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089526-A-G

180950255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089487-G-A

180950255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089487-G-T

180950260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089482-T-A

180950260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089482-T-C

180950372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089425-A-G

180950607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089185-G-A

180950607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089185-G-T

http://identifiers.org/hco/1/GRCh38#180950645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155089140-C-A

180950645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089140-C-T

180950686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089102-G-A

180950686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089102-G-T

http://identifiers.org/hco/1/GRCh38#180950719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155089068-C-A

180950769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155089016-G-T

http://identifiers.org/hco/1/GRCh38#180950795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155088993-C-A

180950795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155088993-C-T

180950852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155088947-G-T

180950935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155088869-A-G

180951493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155088352-G-A

180951493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155088352-G-T

http://identifiers.org/hco/1/GRCh38#180951499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#155088346-C-A

180951499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29327
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 155088346-C-T