http://identifiers.org/hco/6/GRCh38#32292290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34680112-C-A

32292524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34679840-G-A

32292534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34679830-A-G

32292580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34679816-G-A

32292580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34679816-G-C

32292819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34679598-G-T

32292911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34679507-A-G

32293039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34679435-C-T

32293645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34679063-G-C

32294280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34678535-A-G

32294672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34677946-G-C

32294716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34677907-T-C

32299507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34677596-G-A

http://identifiers.org/hco/6/GRCh38#32299807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34677437-C-A

32299807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34677437-C-T

32299831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34677412-A-G

32299960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34677286-G-A

32299960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34677286-G-T

32300656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34676460-G-T

32300681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 34676435-G-T

32304318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34675924-G-A

32304358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34675882-A-T

32315661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34668905-G-A

32315661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34668905-G-T

32315928-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34668637-T-A

32315928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34668637-T-C

32316455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34668190-G-A

32316455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34668190-G-T

32325074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34665222-G-T

http://identifiers.org/hco/6/GRCh38#32325076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34665220-C-A

32325076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34665220-C-T

32325117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34665179-G-C

32325117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34665179-G-T

32326608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34665054-G-C

32332073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34662391-T-G

32332093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34662368-T-C

32332128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34662329-A-G

32332132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34662325-A-G

32332408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34662162-G-C

32334726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34660243-T-C

32335323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34659974-G-A

32335323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34659974-G-T

32335376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34659921-A-G

32335419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34659877-G-A

32335419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34659877-G-T

32335494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34659803-A-G

32335502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34659795-T-C

32335602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34659727-G-T

32336079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34659167-G-T

http://identifiers.org/hco/6/GRCh38#32336573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34658865-A-C

32339052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34656619-T-C

32339052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34656619-T-G

http://identifiers.org/hco/6/GRCh38#32339059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34656580-A-C

32339059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34656580-A-G

32339469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34656231-G-A

32339469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34656231-G-T

32342979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34655390-G-A

32343215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34655210-T-C

32343308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34655111-A-G

http://identifiers.org/hco/6/GRCh38#32355288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34646941-C-A

32355288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34646941-C-T

32366137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34641095-A-T

http://identifiers.org/hco/6/GRCh38#32366252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34640988-C-A

32366255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34640985-A-T

32367272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34640312-A-G

32367866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639444-T-G

32368069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639250-G-A

32368069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639250-G-T

32368533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34638936-G-A

32368744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34638595-G-A

32368744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34638595-G-T

32368849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34638490-T-C

32368860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34638479-A-G

32369959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34637851-G-A

http://identifiers.org/hco/6/GRCh38#32370739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34637263-C-A

32371544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34636646-G-T

http://identifiers.org/hco/6/GRCh38#32371550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34636640-A-C

32371550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34636640-A-G

32371550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34636640-A-T

32371893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34636306-A-G

32372046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34636158-G-A

32372046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34636158-G-T

http://identifiers.org/hco/6/GRCh38#32393727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34585593-C-A

32393727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585593-C-T

32393799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585533-G-A

32393799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585533-G-T

http://identifiers.org/hco/6/GRCh38#32393804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34585528-C-A

32393804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585528-C-G

32393804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585528-C-T

32393846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585504-T-G

32393907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585479-T-G

http://identifiers.org/hco/6/GRCh38#32393938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34585449-C-A

32393938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585449-C-T

32393943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585444-T-C

32393945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585442-T-C

32393950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585437-T-G

32393991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34585422-C-G

32394003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34585410-G-A

http://identifiers.org/hco/6/GRCh38#32394038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34585375-C-A

32394038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34585375-C-T

32394233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585210-C-T

http://identifiers.org/hco/6/GRCh38#32394280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34585180-C-A

32394295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585166-T-C

32394308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585146-C-T

32394430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585035-C-T

32394508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584959-A-T

32394532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584942-A-G

32394542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584932-G-A

32394542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584932-G-C

32394546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584928-G-A

32394555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584918-G-A

32394590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584872-T-A

32394590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584872-T-C

32394590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584872-T-G

http://identifiers.org/hco/6/GRCh38#32394662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34584727-A-C

http://identifiers.org/hco/6/GRCh38#32394675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#34584649-C-A

32394675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584649-C-T

32394702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584474-T-C

32394702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584474-T-G

32395028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 34584152-G-A

32395028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 34584152-G-C

32395028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 34584152-G-T

32395049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34584133-G-A

32395049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34584133-G-T

32395072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34584110-G-T

32395099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34584083-A-G

32395134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34584051-A-G

http://identifiers.org/hco/6/GRCh38#32395156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34584029-C-A

32395156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34584029-C-T

32395176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34584010-T-C

32395273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34583927-A-G

32395542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34583678-C-T

32395862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34582684-T-G

http://identifiers.org/hco/6/GRCh38#32395929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34582619-A-C

32395929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34582619-A-G

http://identifiers.org/hco/6/GRCh38#32395938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34582610-C-A

32395938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34582610-C-T

32395980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34582568-A-T

32396039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 34582511-T-A

32396039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 34582511-T-C

http://identifiers.org/hco/6/GRCh38#32396057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34582493-A-C

32396134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34582416-A-G

32396218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34582332-A-T

http://identifiers.org/hco/6/GRCh38#32396348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34582202-C-A

32396348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34582202-C-T

32396465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34582095-G-T

32401693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34581737-T-C

32401699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34581720-T-C

http://identifiers.org/hco/6/GRCh38#32401725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34581694-C-A

32401725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34581694-C-T

32401762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34581674-G-A

32401762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34581674-G-T

32401789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34581647-C-G

32401906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34581531-A-G

32402108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34581361-G-A

32402566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34580460-A-G

32402600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34580433-G-T

http://identifiers.org/hco/6/GRCh38#32402742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34580302-A-C

http://identifiers.org/hco/6/GRCh38#32402816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34580272-A-C

32402816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34580272-A-G

32402861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34580238-G-A

32402861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34580238-G-T

32402885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34580214-G-T

32403042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34580068-T-C

32403138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579972-C-G

32403159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579951-A-T

http://identifiers.org/hco/6/GRCh38#32403177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34579933-C-A

32403177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579933-C-T

32403229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579830-G-A

32403264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579796-A-G

32403275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579795-G-A

http://identifiers.org/hco/6/GRCh38#32403285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34579786-C-A

32403285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579786-C-T

http://identifiers.org/hco/6/GRCh38#32403545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34579555-C-A

32403595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579456-T-A

32403595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579456-T-C

32403684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579364-G-A

32403764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579302-T-C

32403766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579301-T-C

32403785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579288-T-C

32403785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579288-T-G

32403808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579279-G-T

32403863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579235-G-A

32403863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579235-G-T

http://identifiers.org/hco/6/GRCh38#32404064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34579075-A-C

32404068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34579068-A-G

32404895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34577316-T-G

32404901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34577310-T-C

32404904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34577307-C-T

32404908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34577302-T-G

32404916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34577294-T-C

32404921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34577289-C-G

32404921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34577289-C-T

http://identifiers.org/hco/6/GRCh38#32405119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34577091-C-A

32405119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34577091-C-T

http://identifiers.org/hco/6/GRCh38#32405268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#34576942-C-A

32405268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34576942-C-T

32405820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34576261-T-G

32405906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34576183-T-G

32407089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 34575228-G-T

32407132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 34575185-G-C

32407161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39756
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 34575167-G-T