27534035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 3 prime UTR variant
orthologous variants: 132805145-G-A

27534035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 3 prime UTR variant
orthologous variants: 132805145-G-T

27534084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 3 prime UTR variant
orthologous variants: 132805098-A-G

27534115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 3 prime UTR variant
orthologous variants: 132805069-G-T

27534458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132804750-A-T

27534645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132804561-T-C

27534855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132804357-G-A

27534855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132804357-G-T

27534963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804249-G-A

27534963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804249-G-C

27534963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804249-G-T

27534981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804231-G-A

27534998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804213-A-G

27534998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804213-A-T

27535088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132804107-G-A

27535339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132803129-G-C

27535384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132803085-C-T

27535974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132802606-T-A

27536519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132802086-G-A

http://identifiers.org/hco/1/GRCh38#27536648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132801968-C-A

27536676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801940-G-T

27536852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801785-G-A

27536908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801732-G-C

27537318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801340-G-T

27537605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801039-G-A

27537605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801039-G-C

27537609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132801035-C-T

27537821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132800854-T-C

27537874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132800842-G-A

27537898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132800818-A-G

27540915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799381-C-G

27540915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799381-C-T

http://identifiers.org/hco/1/GRCh38#27541000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132799297-C-A

http://identifiers.org/hco/1/GRCh38#27541060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132799269-A-C

27541060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799269-A-G

27541060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799269-A-T

27541082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799250-C-G

27541082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132799250-C-T

27542522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132798372-C-T

27543097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132797809-G-A

http://identifiers.org/hco/1/GRCh38#27543249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132797657-C-A

27543289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132797617-T-G

27543673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132797293-G-A

27544564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132796660-G-A

27544708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132796515-G-A

27544708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132796515-G-T

27545064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132796228-C-T

27545071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132796221-C-T

27545176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132796122-C-T

27545184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132796114-G-C

http://identifiers.org/hco/1/GRCh38#27545282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132796023-C-A

27545750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132795574-A-G

27545921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132795386-G-A

27546139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132795181-G-A

27546347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132794674-A-G

27547007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132793867-T-C

http://identifiers.org/hco/1/GRCh38#27547173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132793690-C-A

27547173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132793690-C-T

http://identifiers.org/hco/1/GRCh38#27547189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132793664-C-A

27547189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132793664-C-G

27547199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132793654-G-A

27547199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132793654-G-T

27547214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132793635-T-A

27547214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132793635-T-C

27547401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132793446-T-C

http://identifiers.org/hco/1/GRCh38#27547665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132793182-C-A

27547665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132793182-C-T

27547698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132793149-G-A

27547698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132793149-G-T

27547917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132792936-G-T

27548058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132792795-G-A

http://identifiers.org/hco/1/GRCh38#27548178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132792675-C-A

27548178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132792675-C-T

27548316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132792537-C-T

27548421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132792432-C-T

27548643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132792210-G-A

http://identifiers.org/hco/1/GRCh38#27548709-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132792144-A-C

27548751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132792102-T-A

27548751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132792102-T-C

27548958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791904-G-A

27549054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791808-G-A

27549054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791808-G-C

27549054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791808-G-T

27549072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791790-G-A

27549072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791790-G-C

27549072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791790-G-T

27549084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791778-G-A

27549084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 132791778-G-C

27549084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 132791778-G-T

http://identifiers.org/hco/1/GRCh38#27549186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132791676-C-A

27549186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791676-C-T

27549225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791637-G-A

27549474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791388-G-T

27549484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791378-C-G

http://identifiers.org/hco/1/GRCh38#27549510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132791352-C-A

27549510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791352-C-T

27549564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132791298-T-C

27549794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132791071-A-G

27549942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132790923-T-C

http://identifiers.org/hco/1/GRCh38#27550110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132790755-C-A

27550350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132790515-C-T

27550368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132790497-T-A

27550368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132790497-T-C

27550407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132790458-T-C

27550819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132790052-G-T

27550833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132790038-T-C

http://identifiers.org/hco/1/GRCh38#27550893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132789978-C-A

27550893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789978-C-T

27550899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789972-T-C

27550907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132789964-G-A

27550907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132789964-G-T

http://identifiers.org/hco/1/GRCh38#27550908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132789963-C-A

27550908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789963-C-G

27550908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789963-C-T

http://identifiers.org/hco/1/GRCh38#27550926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132789945-C-A

27550926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789945-C-T

27551049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789822-T-A

http://identifiers.org/hco/1/GRCh38#27551073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132789798-A-C

27551073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789798-A-T

27551160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789711-G-A

27551289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789582-A-T

27551316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789555-G-A

27551352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789519-T-C

27551430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789441-G-T

27551459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132789412-C-G

27551459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132789412-C-T

27551460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789411-G-A

27551627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132789244-T-C

27551640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789231-G-A

http://identifiers.org/hco/1/GRCh38#27551760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132789111-C-A

27551760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 132789111-C-T

27551813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132789061-G-A

27551813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132789061-G-C

27551813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 132789061-G-T

27551931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132788943-C-T

27552119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132788755-G-T

27552199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788675-A-T

27552234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788640-T-A

http://identifiers.org/hco/1/GRCh38#27552236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132788638-C-A

27552236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788638-C-T

27552259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788635-A-T

http://identifiers.org/hco/1/GRCh38#27552296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132788605-C-A

27552374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788593-G-A

27552374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788593-G-C

27552374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132788593-G-T

27552772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132788504-G-T

27552779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132788497-A-T

27552788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132788488-A-G

27552795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132788476-T-C

http://identifiers.org/hco/1/GRCh38#27552836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132788418-C-A

27552836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132788418-C-T

27552839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132788415-G-A

27552839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132788415-G-T

http://identifiers.org/hco/1/GRCh38#27552858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132788396-C-A

http://identifiers.org/hco/1/GRCh38#27552867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132788390-C-A

27552867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132788390-C-T

27552902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132788363-G-A

27552902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132788363-G-T

27553238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132788037-T-C

27553422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132787838-A-G

27553474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132787780-G-A

27553474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132787780-G-T

http://identifiers.org/hco/1/GRCh38#27553563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132787690-C-A

27553643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132787623-C-T

27553690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132787577-G-A

27553690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132787577-G-T

27554219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132787391-G-A

27554281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132787323-G-A

27554959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132786564-T-C

27554966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132786557-C-T

27555680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132785390-T-C

27555731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132785345-T-A

27555731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132785345-T-G

27556222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132784877-C-T

27556233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132784865-T-A

27556233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132784865-T-C

27556233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132784865-T-G

27557145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132783842-T-A

27557413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132783570-C-T

http://identifiers.org/hco/1/GRCh38#27557515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132783470-C-A

27558249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132782842-G-C

27558249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132782842-G-T

27558275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132782822-T-C

http://identifiers.org/hco/1/GRCh38#27558374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#132782768-C-A

27558412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132782730-C-T

27558421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132782721-G-A

27558421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132782721-G-T

27558503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132782630-G-A

27558529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 132782605-T-G

http://identifiers.org/hco/1/GRCh38#27558697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132782521-C-A

27558707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 132782511-T-C

27558709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132782509-A-G

27558745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132782475-G-A

27558745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132782475-G-T

http://identifiers.org/hco/1/GRCh38#27558799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132782409-C-A

27558799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 132782409-C-T

http://identifiers.org/hco/1/GRCh38#27558905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132782300-C-A

27558905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132782300-C-G

27558905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132782300-C-T

27558918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132782287-A-G

27558932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132782273-A-G

27558966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132782245-A-G

27558966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132782245-A-T

27559010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132782201-C-T

27559569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132781552-G-A

27559586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132781534-G-C

27560025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132780983-G-C

http://identifiers.org/hco/1/GRCh38#27560238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132780743-C-A

27560343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132780691-G-A

27560726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132780301-C-T

27560976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132780075-C-G

27561325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132779779-G-A

27561325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132779779-G-T

27561339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132779765-G-A

27561347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132779757-G-A

27561347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132779757-G-C

27561347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132779757-G-T

27561569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132779561-G-A

27561569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132779561-G-C

27562121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132779175-C-T

27562195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132779104-G-A

27562244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132779071-C-T

27562328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132778989-G-A

27562390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132778933-G-A

27562391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132778932-C-T

27562581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132778750-C-G

27562581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132778750-C-T

27562630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132778702-G-A

27562690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132778645-T-C

27562909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132778466-C-T

27562936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132778440-C-T

27562950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132778426-C-T

27563647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132778031-G-A

27563833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132777837-T-C

27563846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132777824-T-C

27564254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132777568-T-C

27564542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132777386-C-T

27564598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132777326-T-C

27564638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132777287-T-C

27565522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132776434-T-C

27565538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132776413-A-T

27565586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132776382-A-G

27566613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132775468-G-T

27566636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132775444-G-C

27567528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132774566-C-T

http://identifiers.org/hco/1/GRCh38#27567806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132774302-A-C

27567876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132774225-T-C

27567883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132774218-G-A

27567895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132774206-G-T

27567901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132774193-G-C

27567901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132774193-G-T

http://identifiers.org/hco/1/GRCh38#27568043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132774087-C-A

27568043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132774087-C-T

27568049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132774079-A-G

http://identifiers.org/hco/1/GRCh38#27568154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132774005-C-A

27568154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132774005-C-G

27568154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132774005-C-T

http://identifiers.org/hco/1/GRCh38#27568267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132773897-C-A

27568267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132773897-C-T

27568307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132773862-A-G

27568308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132773861-G-A

27568308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132773861-G-T

27568396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132773771-G-A

27568470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132773699-C-T

http://identifiers.org/hco/1/GRCh38#27568527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#132773645-C-A

http://identifiers.org/hco/1/GRCh38#27569034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132773193-A-C

27569034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132773193-A-G

27569034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132773193-A-T

27569109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132773120-C-G

27569161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132773073-T-G

27569393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132772783-T-C

27569698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132772516-A-G

27569698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132772516-A-T

27571294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132770973-A-G

27571346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132770921-C-T

27571552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132770717-G-T

http://identifiers.org/hco/1/GRCh38#27572037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132770222-C-A

http://identifiers.org/hco/1/GRCh38#27572349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132769906-C-A

27572403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132769851-C-T

http://identifiers.org/hco/1/GRCh38#27572960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132769404-C-A

27573648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132768694-C-T

27574600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767389-A-T

27574603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767387-G-T

27574764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767237-T-A

http://identifiers.org/hco/1/GRCh38#27574781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132767151-C-A

27574781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767151-C-G

27574786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767146-G-C

27574791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767141-G-A

27574814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132767133-G-C

27574942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132767005-T-A

27575037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132766915-G-T

27575151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132766820-G-A

27575435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132766556-C-T

27575664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132766290-G-A

http://identifiers.org/hco/1/GRCh38#27575667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#132766287-C-A

http://identifiers.org/hco/1/GRCh38#27575863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132766105-A-C

27575912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132766068-T-G

27575916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132766065-G-A

27575916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132766065-G-T

27576067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132765936-C-T

27576111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132765892-G-C

27576130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132765872-G-C

27576270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132765739-T-G

27576301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132765708-A-T

27576810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132744426-C-G

27576810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132744426-C-T

27576929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132744270-T-C

27577058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132744150-A-G

27577321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132765302-T-C

27577338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132765285-G-A

27577338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132765285-G-T

27577429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132765208-T-G

27577790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132764815-C-T

27578412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132764233-C-T

27578497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132764165-G-A

27578497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132764165-G-C

27579388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132763857-C-T

27579751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132763398-T-C

http://identifiers.org/hco/1/GRCh38#27580811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132762446-C-A

27580811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132762446-C-T

27581867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132762029-C-T

27581915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132761996-A-G

27581934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132761977-C-T

27582156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132761746-C-T

27582216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132761712-G-A

http://identifiers.org/hco/1/GRCh38#27583268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132760404-A-C

http://identifiers.org/hco/1/GRCh38#27583296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132760376-A-C

27583296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132760376-A-G

27583396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132760290-T-C

27583652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132759894-G-T

27583767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132759431-C-T

http://identifiers.org/hco/1/GRCh38#27583924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132759284-C-A

27584095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132759119-G-A

27584147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132759001-G-A

27584308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132758727-A-G

27584589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132758476-G-T

27584597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132758465-C-T

27584606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132758456-G-C

27584630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132758429-G-A

27584899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132758172-G-A

27585916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132757233-G-C

27585917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132757232-G-C

27585981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132757183-G-A

27586213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132756985-C-G

27586213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132756985-C-T

27586226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132756972-T-G

27586293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132756911-G-A

27586761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132756465-C-T

http://identifiers.org/hco/1/GRCh38#27586815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132756397-A-C

27587166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132756046-C-T

27587198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132756014-A-G

27587547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132755720-G-A

27587569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132755697-G-A

27587906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132755410-C-T

27588139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132754785-C-G

27588139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132754785-C-T

27588225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132754723-G-A

27588671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132754269-T-A

27588993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132753962-G-A

27589136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132753830-T-G

27589206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132753770-C-T

27589237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132753739-G-A

27589484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132753471-G-A

27589484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132753471-G-C

27589498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132753457-C-G

27589698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132753253-G-A

27589838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132753112-T-A

http://identifiers.org/hco/1/GRCh38#27589915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132753035-A-C

27589927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132753019-T-A

27589927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132753019-T-C

27590295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132752649-C-T

27590556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132752411-A-G

27590568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132752400-T-A

http://identifiers.org/hco/1/GRCh38#27591061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132751956-C-A

27591167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132751850-T-C

http://identifiers.org/hco/1/GRCh38#27591217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132751803-C-A

27591266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132751753-G-C

27591283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132751736-G-A

27591642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132751361-G-A

27591774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132751243-T-C

27591813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132751204-G-C

27591961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132751054-G-T

27592281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132750732-C-T

27592400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132750612-G-A

27592569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132750443-C-G

27592569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132750443-C-T

27592574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132750437-T-A

27592574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132750437-T-C

27592574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132750437-T-G

27592693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132750320-T-C

27592752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132750263-G-A

27592978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132750037-C-T

27593157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132749862-G-A

27593444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132749541-G-A

27593652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132749371-C-T

27593673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132749351-C-T

27594393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132748696-C-T

27594421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132748674-G-A

27594618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132748483-G-A

27594619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132748482-G-C

27594741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132748381-T-C

27594759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132748366-G-A

27594759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132748366-G-C

27594847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132748273-G-A

27595000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132748098-G-A

27595000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132748098-G-C

27595112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132747989-T-C

27595205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132747911-A-G

27595471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132747692-A-T

27595878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132747268-G-A

27595878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132747268-G-C

27595945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 132747199-G-T

27596252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132746902-C-G

27596361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132746792-T-C

27596505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132746624-G-A

http://identifiers.org/hco/1/GRCh38#27596582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132746547-C-A

27596740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132746361-C-T

27596749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132746351-C-T

27596762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132746338-G-C

27597227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132745755-G-A

27597512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132745553-G-A

27597695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132745381-A-T

27598252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132744791-A-G

27598294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132744751-G-T

27598771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132744284-A-G

27599622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132743456-A-G

27599622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 132743456-A-T

27599765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132743310-T-G

27599792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132743289-G-A

http://identifiers.org/hco/1/GRCh38#27599910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132743175-C-A

27599910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132743175-C-T

http://identifiers.org/hco/1/GRCh38#27599959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132743122-A-C

27600703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132742312-C-G

http://identifiers.org/hco/1/GRCh38#27600820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132742216-C-A

27600855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132742179-G-C

27600936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132742101-C-T

27601010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132742024-C-T

27601297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132741736-G-T

http://identifiers.org/hco/1/GRCh38#27601381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132741651-C-A

27601381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132741651-C-T

27601647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132741406-G-A

27601647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132741406-G-C

27601873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132741130-A-G

27602759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132740229-C-T

27603092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132739902-G-A

http://identifiers.org/hco/1/GRCh38#27603154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132739840-C-A

27603154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132739840-C-G

http://identifiers.org/hco/1/GRCh38#27603162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132739832-C-A

27603162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132739832-C-G

27603277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 132739717-C-T

27603534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 132739459-C-T

http://identifiers.org/hco/1/GRCh38#27603619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#132739373-C-A

27603619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 132739373-C-T

http://identifiers.org/hco/1/GRCh38#27603670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132739323-C-A

27604024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 132738972-T-C

http://identifiers.org/hco/1/GRCh38#27604165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#132738827-C-A

27604165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 132738827-C-T

http://identifiers.org/hco/1/GRCh38#27604225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#132738767-C-A

27604292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 132738701-A-T

http://identifiers.org/hco/1/GRCh38#27604305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#132738693-C-A

27604305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 132738693-C-G

27604305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 132738693-C-T

27604323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non coding transcript exon variant
orthologous variants: 132738676-T-C

27604427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non coding transcript exon variant
orthologous variants: 132738573-A-G

27604427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25230
most severe consequence: non coding transcript exon variant
orthologous variants: 132738573-A-T