http://identifiers.org/hco/8/GRCh38#143309344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75528878-C-A

143309344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75528878-C-G

143309344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75528878-C-T

http://identifiers.org/hco/8/GRCh38#143309352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75528889-C-A

143309632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 75529131-C-G

143309754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75529238-C-T

143309834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75529297-T-A

143309834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75529297-T-C

143309834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75529297-T-G

143309841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75529304-C-T

143309966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 75529444-G-A

143310041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 75529507-G-A

143310041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 75529507-G-T

143310138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75529603-C-T

http://identifiers.org/hco/8/GRCh38#143310156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75529621-C-A

143310156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75529621-C-T

143310168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 75529633-C-T

http://identifiers.org/hco/8/GRCh38#143310184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75529649-C-A

http://identifiers.org/hco/8/GRCh38#143310234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75529693-A-C

143310262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75529713-G-A

143310262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75529713-G-T

143310282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75529738-C-T

http://identifiers.org/hco/8/GRCh38#143310355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75529801-A-C

143310355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75529801-A-G

http://identifiers.org/hco/8/GRCh38#143310356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75529802-A-C

http://identifiers.org/hco/8/GRCh38#143310357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75529803-A-C

143310472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 75529885-G-A

143310519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75529907-G-A

143310519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75529907-G-T

143310537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75529928-G-A

143310537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75529928-G-T

143310604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 75529986-G-T

143315678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron variant
orthologous variants: 75535151-G-A

143315688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron variant
orthologous variants: 75535161-G-A

143315688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron variant
orthologous variants: 75535161-G-C

143315688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron variant
orthologous variants: 75535161-G-T

143315703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron variant
orthologous variants: 75535176-G-A

143315844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron variant
orthologous variants: 75535323-G-A

143316029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75535894-G-A

143316029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75535894-G-C

143316068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75535933-G-A

143316132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 75536000-A-G

143317189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537025-G-A

143317341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537097-G-A

143317529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537277-G-A

143317529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537277-G-C

143317581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537336-G-A

143317581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537336-G-T

143317600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537353-A-G

143317606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537359-T-C

143317633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537366-G-A

143317633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537366-G-T

143317647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537376-G-A

143317647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537376-G-T

143317667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537384-T-A

http://identifiers.org/hco/8/GRCh38#143317685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75537402-C-A

143317689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537406-C-T

143317763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75537476-G-A

143317763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75537476-G-C

143317934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75537656-A-G

143318109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75538196-C-T

143318130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75538217-A-G

143318145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75538239-G-A

143318145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75538239-G-T

143318189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75538305-T-G

http://identifiers.org/hco/8/GRCh38#143318201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75538319-C-A

143318201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75538319-C-T

143318292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75538412-A-G

143318414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75538531-C-T

143318416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75538533-C-T

http://identifiers.org/hco/8/GRCh38#143321103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75539179-A-C

143321103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75539179-A-T

143321105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75539181-A-G

143321127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75539205-G-A

143321127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75539205-G-C

143321127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75539205-G-T

143321163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75539244-T-C

http://identifiers.org/hco/8/GRCh38#143321213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75539281-C-A

143321213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75539281-C-T

143321293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75539361-G-A

143321342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75539410-G-A

143321342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75539410-G-C

http://identifiers.org/hco/8/GRCh38#143321434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75539513-C-A

143321434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75539513-C-T

http://identifiers.org/hco/8/GRCh38#143321450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75539534-C-A

143321450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75539534-C-T

http://identifiers.org/hco/8/GRCh38#143321493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75539568-C-A

143321493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75539568-C-T

143321496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75539571-G-A

143324075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75539747-G-A

143324075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75539747-G-C

143324106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75539778-G-A

143324106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75539778-G-T

143324156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75539828-A-G

143324156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75539828-A-T

143324352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75540318-G-T

143324399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75540364-G-T

http://identifiers.org/hco/8/GRCh38#143324424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75540387-C-A

143324424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75540387-C-T

http://identifiers.org/hco/8/GRCh38#143324445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75540422-C-A

143324489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75540479-A-G

143324497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75540487-G-A

143324562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 75540552-T-A

143324645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75540650-G-A

143324645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75540650-G-C

143324718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75540715-G-A

143324718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75540715-G-T

http://identifiers.org/hco/8/GRCh38#143324750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75540747-C-A

143324750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75540747-C-T

143325174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541036-G-A

143325178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541040-G-A

143325278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541066-G-T

143325326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541106-C-T

143325332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541115-G-A

143325332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541115-G-T

143325485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 75541275-T-C

143325485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 75541275-T-G

143325489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 75541279-G-A

143325489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 75541279-G-T

http://identifiers.org/hco/8/GRCh38#143325558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75541345-A-C

143325558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541345-A-G

143325794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541506-A-G

143325936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541637-C-T

143325945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541646-T-C

143326024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541693-C-G

143326024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541693-C-T

143326075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541752-T-C

143326175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541867-G-A

143326175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541867-G-T

143326185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541877-G-A

143326185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541877-G-T

143326208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541901-C-G

143326208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75541901-C-T

143326364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75542055-G-A

143326364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75542055-G-C

143326364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75542055-G-T

143329271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75546071-T-C

143329276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75546076-G-A

143329276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75546076-G-T

143329298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75546095-C-T

143329414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, missense_variant, start_lost
orthologous variants: 75546205-A-G

143329434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75546225-G-A

143329491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75546280-C-T

http://identifiers.org/hco/8/GRCh38#143329506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75546294-C-A

143329506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75546294-C-T

http://identifiers.org/hco/8/GRCh38#143329516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75546304-C-A

http://identifiers.org/hco/8/GRCh38#143331172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75547814-C-A

143331172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75547814-C-T

http://identifiers.org/hco/8/GRCh38#143331184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75547826-C-A

143331184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75547826-C-T

143331196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75547841-G-A

143331200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75547845-A-G

143331207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75547852-G-A

143331207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75547852-G-T

143331228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75547872-A-G

143331267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75547911-G-A

143331267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75547911-G-C

143331297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 75547941-C-T

143331605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548157-G-A

143331605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548157-G-C

143331605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548157-G-T

143331623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548167-G-A

143331623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548167-G-T

143331630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548174-G-A

143331630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548174-G-T

http://identifiers.org/hco/8/GRCh38#143331649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75548193-C-A

143331663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548204-C-T

143331752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 75548272-T-C

143331812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548306-G-A

143331812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548306-G-T

143331815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548309-A-G

143331931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548377-A-G

143332237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548662-T-C

143332269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548687-C-G

143332269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548687-C-T

143332270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548688-G-A

143332306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548726-G-A

143332306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548726-G-C

143332306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 75548726-G-T

143340528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron variant
orthologous variants: 75552500-C-T

143340613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron variant
orthologous variants: 75552583-C-T

143340709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron variant
orthologous variants: 75552711-T-C

143340782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron variant
orthologous variants: 75552773-T-C

143340847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron variant
orthologous variants: 75552867-G-T

143345187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75553763-G-A

143345287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75553870-G-A

143355057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75561676-G-A

143355057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75561676-G-C

143355206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75561788-G-A

143355347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75561935-T-C

143355348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75561936-G-A

143355348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75561936-G-C

143355348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75561936-G-T

143355390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75561967-A-G

143355791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75562428-C-T

143355864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75562479-A-G

143355864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75562479-A-T

http://identifiers.org/hco/8/GRCh38#143355892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75562505-C-A

143355892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75562505-C-T

143355893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75562506-T-C

143358530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564215-T-A

143358530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564215-T-C

http://identifiers.org/hco/8/GRCh38#143358590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75564275-C-A

143358590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75564275-C-T

143358594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75564279-A-G

143358632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75564315-G-A

http://identifiers.org/hco/8/GRCh38#143358641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75564323-C-A

143358641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75564323-C-T

http://identifiers.org/hco/8/GRCh38#143358678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75564347-A-C

143358678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564347-A-G

143358678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564347-A-T

143358693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564362-G-T

http://identifiers.org/hco/8/GRCh38#143358781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#75564456-C-A

143358781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564456-C-G

143358781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29787
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75564456-C-T