103414842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 38975801-G-A

http://identifiers.org/hco/8/GRCh38#103414950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#38975909-C-A

103414950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 38975909-C-G

103414950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 38975909-C-T

103414952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38975911-T-C

103414976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38975935-C-T

103415005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 38975964-A-G

http://identifiers.org/hco/8/GRCh38#103415037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#38976010-C-A

103415037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38976010-C-T

103415104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38976043-T-A

103415104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 38976043-T-C

103415162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 38976077-G-A

103415170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 38976085-G-A

103415170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 38976085-G-C

103415219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense_variant, undefined
orthologous variants: 38976151-G-A

103415219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense_variant, undefined
orthologous variants: 38976151-G-C

103415231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense_variant, undefined
orthologous variants: 38976163-G-A

103415240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense_variant, undefined
orthologous variants: 38976172-T-C

103415240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense_variant, undefined
orthologous variants: 38976172-T-G

103415257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: synonymous variant
orthologous variants: 38976188-G-A

103415275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: synonymous_variant, undefined
orthologous variants: 38976206-C-T

103415276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense_variant, undefined
orthologous variants: 38976207-C-G

103415276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense_variant, undefined
orthologous variants: 38976207-C-T

103415277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense_variant, undefined
orthologous variants: 38976208-G-T

103415295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense variant
orthologous variants: 38976226-C-T

103415303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense_variant, undefined
orthologous variants: 38976234-C-G

103415318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense_variant, undefined
orthologous variants: 38976249-G-A

103415335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense_variant, undefined
orthologous variants: 38976267-T-A

103415433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38976363-G-T

103415543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38976473-G-A

103415546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38976476-G-A

103415546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38976476-G-T

103415576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38976504-G-T

103417066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980541-G-C

http://identifiers.org/hco/8/GRCh38#103417097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38980572-C-A

103417197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980661-A-G

103417227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980690-G-C

103417228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980691-C-T

103417375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980875-C-T

http://identifiers.org/hco/8/GRCh38#103417416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38980915-C-A

103417416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980915-C-T

103417417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980916-G-A

103417417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980916-G-T

103418109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980976-C-T

http://identifiers.org/hco/8/GRCh38#103418114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38980981-C-A

103418114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980981-C-G

103418114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38980981-C-T

103418161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38981119-A-G

103419391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38981559-C-T

103419466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38981629-G-C

103419636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38981773-G-A

103419706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38981844-G-A

103420123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38981956-G-T

103420167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982000-A-G

103420173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982006-T-C

103420247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982089-G-T

http://identifiers.org/hco/8/GRCh38#103420364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38982206-A-C

http://identifiers.org/hco/8/GRCh38#103420434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38982276-A-C

103420454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38982296-T-C

103420500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38982335-T-C

103420658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982455-A-G

103420780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982553-G-A

103420780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982553-G-C

103420824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982596-A-G

http://identifiers.org/hco/8/GRCh38#103420933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38982704-C-A

103420933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982704-C-T

103421016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38982781-A-G

103421037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38982802-T-C

103421177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982940-T-C

103421177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982940-T-G

103421232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38982990-T-A

http://identifiers.org/hco/8/GRCh38#103421281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38983071-C-A

103421281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983071-C-G

103421282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983072-T-A

103421282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983072-T-C

103421350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983134-G-T

103421355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983139-T-C

http://identifiers.org/hco/8/GRCh38#103421383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38983167-C-A

103421464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983240-C-G

103421464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983240-C-T

103421592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983356-C-T

103421622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983384-T-A

103422067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983812-A-G

103422155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983896-G-A

103422164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983904-A-G

103422168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38983908-G-A

103425691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986241-C-T

103426158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986709-A-G

http://identifiers.org/hco/8/GRCh38#103426175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38986726-C-A

103426175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986726-C-T

103426242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986794-G-A

103426366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38986893-G-T

103426712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987252-A-G

103426831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987363-A-T

http://identifiers.org/hco/8/GRCh38#103426953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38987483-C-A

103426953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987483-C-T

103427011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987534-T-C

103427015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987538-A-G

http://identifiers.org/hco/8/GRCh38#103427073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38987696-C-A

103427073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38987696-C-G

103427354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38987960-G-A

103427354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38987960-G-T

103427420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988046-A-G

http://identifiers.org/hco/8/GRCh38#103427421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38988047-C-A

103427755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988365-G-C

103427755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988365-G-T

http://identifiers.org/hco/8/GRCh38#103427771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38988379-C-A

103427771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988379-C-T

http://identifiers.org/hco/8/GRCh38#103427856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38988460-C-A

http://identifiers.org/hco/8/GRCh38#103427913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38988516-C-A

103427913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988516-C-T

103427958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988562-T-C

103428029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988597-C-T

103428042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988610-A-G

103428113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988676-G-A

103428127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988690-G-A

103428154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988719-A-G

http://identifiers.org/hco/8/GRCh38#103428180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38988745-C-A

103428180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988745-C-T

103428199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988764-A-G

http://identifiers.org/hco/8/GRCh38#103428237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38988784-C-A

103428281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988832-T-C

103428314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38988849-A-T

103428479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38989003-T-C

http://identifiers.org/hco/8/GRCh38#103428538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38989062-C-A

103428538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38989062-C-T

103428560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38989084-C-T

103428652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38989322-T-C

103428745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38989412-T-A

103428745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38989412-T-G

103428760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38989427-G-T

103428931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38989583-C-G

103429214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38989859-T-C

103429314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38989980-A-G

103429400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38990056-G-T

http://identifiers.org/hco/8/GRCh38#103429406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38990062-C-A

103429456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38990106-A-T

http://identifiers.org/hco/8/GRCh38#103429498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38990147-C-A

103429518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38990167-G-T

http://identifiers.org/hco/8/GRCh38#103430424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38991087-A-C

103430424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38991087-A-G

http://identifiers.org/hco/8/GRCh38#103430760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38991425-C-A

103430778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38991437-T-C

http://identifiers.org/hco/8/GRCh38#103430780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38991439-C-A

103430835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38991493-G-A

103430835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38991493-G-T

103431044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38991621-C-G

http://identifiers.org/hco/8/GRCh38#103431152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38991720-C-A

103431356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38991921-A-G

103431404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38991971-T-G

103432266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993220-T-G

103432347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993299-T-C

103432448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993401-T-C

103432478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993431-T-C

103432478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993431-T-G

103432516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993462-A-G

103432547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993489-G-A

103432547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993489-G-T

http://identifiers.org/hco/8/GRCh38#103432623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38993537-A-C

103432623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993537-A-G

103432736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38993688-T-C

103432769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993717-G-A

http://identifiers.org/hco/8/GRCh38#103432825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#38993772-C-A

103432825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993772-C-G

103432825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38993772-C-T

103433247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38994116-G-A

103433247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38994116-G-C

http://identifiers.org/hco/8/GRCh38#103435573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39001427-C-A

103435847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39001706-A-G

103435847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39001706-A-T

http://identifiers.org/hco/8/GRCh38#103435940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39001797-C-A

103435940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39001797-C-T

103436148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39002092-A-G

103436150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39002123-A-G

http://identifiers.org/hco/8/GRCh38#103436661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39002753-C-A

103436704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39002801-G-A

103439932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39006799-T-C

http://identifiers.org/hco/8/GRCh38#103439975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39006855-C-A

http://identifiers.org/hco/8/GRCh38#103440030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39006910-A-C

103440030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39006910-A-G

103440030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39006910-A-T

http://identifiers.org/hco/8/GRCh38#103440103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39006985-C-A

103440103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39006985-C-G

103440103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39006985-C-T

103440285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39007165-T-C

http://identifiers.org/hco/8/GRCh38#103440408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39007269-A-C

103440408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39007269-A-G

http://identifiers.org/hco/8/GRCh38#103440413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39007274-C-A

103440413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39007274-C-T

103440420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39007281-G-T

http://identifiers.org/hco/8/GRCh38#103440491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39007473-C-A

103440568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39007642-G-A

103440605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39007680-G-T

103440667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39007741-A-G

http://identifiers.org/hco/8/GRCh38#103440811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39007845-C-A

103440863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39007901-A-G

http://identifiers.org/hco/8/GRCh38#103440924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39007949-C-A

103441144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39008177-T-C

103441164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39008205-T-C

103441237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39008289-G-A

103441237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39008289-G-T

http://identifiers.org/hco/8/GRCh38#103441279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39008328-C-A

103441279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39008328-C-G

103441381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39008415-G-A

103441381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39008415-G-C

103441381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39008415-G-T

103441402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39008435-A-G

103441642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39008679-T-C

103442750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39010018-A-G

103442832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39010105-G-A

http://identifiers.org/hco/8/GRCh38#103442837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39010110-A-C

103442837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39010110-A-G

103442837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39010110-A-T

103442958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 39010234-G-T

103442981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24535
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 39010257-T-C