43723040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94415941-G-T

43723083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94415987-T-C

http://identifiers.org/hco/12/GRCh38#43723290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94416186-C-A

43723372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94416267-G-A

43723430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94416326-G-T

43723496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94416392-G-C

43723496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94416392-G-T

43723499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94416395-G-A

http://identifiers.org/hco/12/GRCh38#43723613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94416514-C-A

http://identifiers.org/hco/12/GRCh38#43725707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94417528-A-C

43725724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94417545-A-G

http://identifiers.org/hco/12/GRCh38#43728159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94418436-C-A

43728262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94418529-G-T

43728277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94418546-G-C

43728360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94418617-G-T

43728368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94418625-A-G

43728394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94418654-T-C

43728574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94418830-T-C

43729477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94420466-G-T

43729478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94420467-G-T

43729593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94420572-T-C

43729650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94420616-A-G

43729751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94420712-G-T

43730124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94420986-G-T

43730163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94421022-A-G

http://identifiers.org/hco/12/GRCh38#43730204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94421054-C-A

http://identifiers.org/hco/12/GRCh38#43730207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94421057-A-C

43730257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94421093-G-A

43730257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94421093-G-T

43730339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94421163-G-T

43730347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94421171-T-C

43730347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3 prime UTR variant
orthologous variants: 94421171-T-G

43730412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: synonymous variant
orthologous variants: 94421236-G-A

43730492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense variant
orthologous variants: 94421316-T-C

43730538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: synonymous variant
orthologous variants: 94421368-G-C

43730588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense variant
orthologous variants: 94421418-T-C

43730588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense variant
orthologous variants: 94421418-T-G

43730648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: stop gained
orthologous variants: 94421478-G-A

http://identifiers.org/hco/12/GRCh38#43730752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94421584-C-A

43730752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94421584-C-T

43730759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94421591-A-T

43730779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94421607-T-C

43730866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94421695-T-C

43730927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94421752-C-G

43730951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94421776-C-G

43731101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94421918-T-G

43731240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94422040-C-T

43731671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94423638-G-T

43731700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94423667-T-C

43731790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94423758-T-A

43731790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94423758-T-C

43731796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94423764-A-G

http://identifiers.org/hco/12/GRCh38#43731797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94423765-A-C

43731797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94423765-A-T

43731898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94423846-T-C

43732042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94423976-T-C

43732075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94423981-G-A

43732522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94424102-G-A

43732526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94424106-C-T

43732561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94424145-C-T

43734433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94424275-G-T

43734462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94424300-C-G

43734621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94424446-C-G

43734622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94424447-A-G

43734707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94424514-G-A

http://identifiers.org/hco/12/GRCh38#43734830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94424619-A-C

43734853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94424644-C-T

43734902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94424700-C-T

43734904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94424702-G-A

43734974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94424766-G-A

43736252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: 94425618-T-A

http://identifiers.org/hco/12/GRCh38#43736254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94425620-A-C

http://identifiers.org/hco/12/GRCh38#43736369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94425667-A-C

43736401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 94425698-C-T

43736402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 94425699-G-A

43736546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 94425840-G-A

43736555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 94425849-C-T

43736560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 94425854-T-C

http://identifiers.org/hco/12/GRCh38#43736564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94425858-A-C

43736573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 94425867-G-A

43736573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 94425867-G-C

43736579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 94425873-G-T

43736630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94425924-A-G

43736638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94425932-A-G

43736638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94425932-A-T

43736690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94425980-T-C

43736718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94426009-A-G

43736759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94426038-G-A

43736759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94426038-G-C

43736759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94426038-G-T

43736770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94426054-G-A

43736770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94426054-G-T

http://identifiers.org/hco/12/GRCh38#43736781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94426065-C-A

43736781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94426065-C-T

43736787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94426071-G-A

43736787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94426071-G-T

http://identifiers.org/hco/12/GRCh38#43736841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94426101-C-A

43736860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94426123-G-A

43736860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94426123-G-C

43737186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94426404-C-T

http://identifiers.org/hco/12/GRCh38#43738054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94427060-C-A

43738054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94427060-C-T

http://identifiers.org/hco/12/GRCh38#43738111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94427117-C-A

http://identifiers.org/hco/12/GRCh38#43738169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94427169-A-C

43738169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94427169-A-G

43738181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94427181-A-G

43738186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94427186-G-A

43738203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94427203-A-T

43738209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94427211-T-A

43738209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94427211-T-C

43738209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94427211-T-G

43738410-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 94427437-T-A

43738410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 94427437-T-C

43738454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94427483-A-G

43738486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94427509-G-T

43742162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429185-G-C

43742268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429286-C-T

http://identifiers.org/hco/12/GRCh38#43742305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94429321-C-A

43742305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429321-C-G

43742305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429321-C-T

43742377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429391-G-A

43742377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429391-G-T

43742384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429398-A-G

43742410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429413-G-A

43742410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429413-G-T

43742418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429421-G-T

43742560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94429558-G-A

43742560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94429558-G-T

43742564-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429562-A-T

43742582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429581-T-G

http://identifiers.org/hco/12/GRCh38#43742616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94429600-C-A

43742616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429600-C-T

http://identifiers.org/hco/12/GRCh38#43742637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94429621-A-C

43742695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429679-T-A

http://identifiers.org/hco/12/GRCh38#43742696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94429680-C-A

43742705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429689-G-A

43742705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429689-G-T

43742951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430010-T-A

43742951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430010-T-C

43743285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430248-C-G

43743335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430296-G-A

43743379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430340-C-G

http://identifiers.org/hco/12/GRCh38#43746080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94431399-C-A

43746106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94431425-T-C

43746117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94431436-T-C

43746145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94431464-T-C

http://identifiers.org/hco/12/GRCh38#43746169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94431488-A-C

43746169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94431488-A-G

43746173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94431492-T-A

43746173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94431492-T-C

http://identifiers.org/hco/12/GRCh38#43746182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94431501-C-A

43746182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94431501-C-T

43746189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94431508-T-A

43746189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94431508-T-C

43746213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94431532-C-T

43746214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94431533-A-G

http://identifiers.org/hco/12/GRCh38#43746225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#94431544-C-A

43746225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94431544-C-G

43746225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94431544-C-T

43746256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94431575-T-A

43746256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94431575-T-C

43746265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94431582-A-G

43746917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94432947-C-G

43746917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94432947-C-T

43746959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94432993-A-G

43746961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94432995-C-T

43747144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433343-T-C

43747186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433380-A-G

43747282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433475-A-G

43748292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433850-G-A

43748346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433920-A-G

43748346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433920-A-T

http://identifiers.org/hco/12/GRCh38#43748392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94433961-A-C

http://identifiers.org/hco/12/GRCh38#43748415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94433988-A-C

43748415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433988-A-G

43748420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433993-C-G

http://identifiers.org/hco/12/GRCh38#43748625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94434568-A-C

43748625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94434568-A-T

43748628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94434571-T-C

http://identifiers.org/hco/12/GRCh38#43748678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94434620-C-A

43748680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94434622-G-A

43748680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94434622-G-T

43748695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94434637-T-C

43753136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94436771-G-A

43753153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94436788-A-G

43753179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94436838-T-A

43753651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437273-T-C

43753731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437363-G-A

43753800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437437-A-G

43753977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437659-T-C

43754030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437706-T-G

43754034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437710-T-G

43754066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437742-T-A

43754273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437885-T-C

43754375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94437976-G-A

43754415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94438010-T-C

43754487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94438082-A-G

43754577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94438172-A-G

43754623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94438218-T-C

43754623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94438218-T-G

43754649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94438244-T-C

43754694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94438289-T-C

43754694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94438289-T-G

43754830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94438425-T-C

http://identifiers.org/hco/12/GRCh38#43754844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94438439-A-C

43754844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94438439-A-G

43754951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 94438549-G-A

43754999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94438597-C-T

43755069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94438667-T-G

43755091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94438689-T-A

43755091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94438689-T-C

43755096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94438694-G-A

http://identifiers.org/hco/12/GRCh38#43755135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94438733-A-C

43755135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94438733-A-T

http://identifiers.org/hco/12/GRCh38#43755257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94438851-A-C

http://identifiers.org/hco/12/GRCh38#43755275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94438869-C-A

http://identifiers.org/hco/12/GRCh38#43755316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#94438903-C-A

43755316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438903-C-T

43755329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438916-G-C

43755329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438916-G-T

43758739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94441350-G-A

43758746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94441358-G-A

43758746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94441358-G-T

43758785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94441398-T-A

43758785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94441398-T-C

43758793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 5 prime UTR variant
orthologous variants: 94441406-T-A

43758793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25276
most severe consequence: 5 prime UTR variant
orthologous variants: 94441406-T-C