106490551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8668245-T-A

106490590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8668284-T-C

106490612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8668302-T-C

106490889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8668570-T-C

http://identifiers.org/hco/13/GRCh38#106491107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8668788-C-A

http://identifiers.org/hco/13/GRCh38#106491129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8668805-C-A

106491232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8668909-A-G

106491551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8669241-T-C

106491631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8669318-C-T

106491633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8669320-G-A

106491633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8669320-G-T

106491827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8669494-G-A

106491827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8669494-G-T

106492228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8669868-T-C

106492230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8669870-G-A

106492230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8669870-G-T

106492247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8669887-T-C

106492281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8669923-A-G

106492281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8669923-A-T

http://identifiers.org/hco/13/GRCh38#106492300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8669942-C-A

106492310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8669951-G-T

http://identifiers.org/hco/13/GRCh38#106492346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8669974-C-A

106492346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8669974-C-T

http://identifiers.org/hco/13/GRCh38#106492390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8670000-C-A

106492462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 8670068-T-G

106492591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8670208-G-A

106492591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8670208-G-T

106492620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8670237-T-A

106492665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8670272-G-T

106492931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8670513-G-A

106492931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8670513-G-T

106493109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8670657-G-A

http://identifiers.org/hco/13/GRCh38#106493166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8670714-C-A

106493166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8670714-C-T

http://identifiers.org/hco/13/GRCh38#106493500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8671038-C-A

106493500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8671038-C-T

106493664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8671163-C-T

106494137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8671618-A-G

http://identifiers.org/hco/13/GRCh38#106494214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8671693-C-A

106494251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8671762-C-T

http://identifiers.org/hco/13/GRCh38#106494375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8671860-C-A

http://identifiers.org/hco/13/GRCh38#106494562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8672036-A-C

http://identifiers.org/hco/13/GRCh38#106494596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8672070-A-C

106494619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672091-G-T

106494758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672224-A-G

106494758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672224-A-T

106494759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672225-T-G

106494779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672241-T-C

106494792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672254-G-A

106494792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672254-G-T

106494795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672257-G-A

106494795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672257-G-T

106494921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 8672371-T-G

106495123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672572-A-T

106495171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672620-T-C

106495357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8672794-T-C

106496369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8673764-A-G

106497021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8674378-A-G

106497277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8674613-T-C

106497302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8674635-T-A

106497307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8674640-T-A

106497405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8674744-T-C

106497426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8674754-A-G

106497446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8674772-T-A

http://identifiers.org/hco/13/GRCh38#106497457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8674783-C-A

106497468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8674791-A-G

106497809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8674918-G-A

106497809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8674918-G-T

106497823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8674934-G-A

106498144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8675217-A-G

106498560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8675683-A-T

106498620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8675749-C-T

106498655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8675785-T-A

106498681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8675821-G-A

http://identifiers.org/hco/13/GRCh38#106498804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8676059-A-C

106498916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8676220-T-C

106498931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8676233-T-A

106498950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8676249-C-G

106498960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8676259-G-C

106499290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8676604-A-T

106499586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8677296-T-G

106499614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8677324-T-A

106499639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8677349-A-T

106499712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8677425-T-C

http://identifiers.org/hco/13/GRCh38#106499718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8677435-A-C

106499718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8677435-A-G

106499890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8677776-G-A

http://identifiers.org/hco/13/GRCh38#106499939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8677835-C-A

106499939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8677835-C-T

106500066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8678017-G-C

106500198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8678142-T-C

106500734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8678570-A-T

106500892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8678683-G-A

106500939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8678720-G-A

106500939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8678720-G-C

106501042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8678832-T-C

106501144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8678959-G-A

106502088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8679680-T-C

106502467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8680060-C-T

106502811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8680249-T-C

http://identifiers.org/hco/13/GRCh38#106502902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8680362-C-A

106503310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8680756-G-A

http://identifiers.org/hco/13/GRCh38#106503943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8681255-A-C

106504011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8681315-C-T

106504056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8681359-A-T

http://identifiers.org/hco/13/GRCh38#106504526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8681818-C-A

106504544-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8681839-A-T

106504904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8682354-T-C

106505032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8682542-G-T

106505246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8682827-G-A

http://identifiers.org/hco/13/GRCh38#106505379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8683001-A-C

106505607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8683229-T-G

106505870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8683589-A-G

106505870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8683589-A-T

http://identifiers.org/hco/13/GRCh38#106505936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8683721-C-A

106505936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8683721-C-T

http://identifiers.org/hco/13/GRCh38#106505955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8683740-C-A

106505955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8683740-C-T

106505956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8683741-A-G

http://identifiers.org/hco/13/GRCh38#106505963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8683748-C-A

106505966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8683751-A-G

106506104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8683860-C-T

106506141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8683890-T-C

106506331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8683938-G-A

106506598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8684191-A-G

106506634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8684224-T-A

http://identifiers.org/hco/13/GRCh38#106506790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8684381-C-A

106506790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8684381-C-G

106506790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 8684381-C-T

106507294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8684851-A-G

106507385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8684955-C-T

http://identifiers.org/hco/13/GRCh38#106507422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8684990-A-C

106508529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8685938-G-A

106508810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8686054-G-A

106509332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8686479-T-C

106509848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8686905-T-C

106510074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8687150-A-G

106510284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8687398-T-C

http://identifiers.org/hco/13/GRCh38#106511213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8687934-C-A

106512070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8688760-C-T

106512074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8688764-C-T

106512098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8688792-A-T

http://identifiers.org/hco/13/GRCh38#106512440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8689118-C-A

106512440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8689118-C-G

106512440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8689118-C-T

106512441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8689119-A-G

106512489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8689166-T-G

106512513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8689190-A-G

106512587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 8689264-T-A

106512906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8689581-A-T

106513075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8689697-C-T

106513123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8689745-A-G

106514120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8690962-C-T

106514326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8691420-G-T

106514558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8691601-C-T

106514596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8691661-T-C

106514685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8691752-A-G

106514725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8691793-A-G

106514768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8691844-A-G

106514819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8691901-G-A

106514840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8691922-T-C

106514842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8691924-G-C

106515110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8692199-T-C

http://identifiers.org/hco/13/GRCh38#106515113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8692202-A-C

106515168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8692266-T-A

106515209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8692312-C-G

http://identifiers.org/hco/13/GRCh38#106515394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#8692467-C-A

106515394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8692467-C-T

106515400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 8692473-T-C

106515413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8692481-C-T

106515896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8693568-G-A

106516068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 8693742-G-C

http://identifiers.org/hco/13/GRCh38#106516098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8693772-C-A

106516194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8693866-G-T

http://identifiers.org/hco/13/GRCh38#106516344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8693968-C-A

106516344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 8693968-C-T

http://identifiers.org/hco/13/GRCh38#106516520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8694131-C-A

106516528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8694139-G-T

106516700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8694319-T-C

106516875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8694451-T-C

106517671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8694757-T-A

http://identifiers.org/hco/13/GRCh38#106517683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8694769-A-C

106517691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8694777-G-C

106517795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8694884-G-C

106517795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8694884-G-T

106517796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8694885-G-A

106517796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8694885-G-T

106517815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8694903-C-G

106519846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8696663-C-T

106520127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8696924-T-C

106520237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8697022-C-T

http://identifiers.org/hco/13/GRCh38#106520379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8697149-C-A

106520379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8697149-C-T

106520449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8697168-G-A

106520485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8697202-C-T

http://identifiers.org/hco/13/GRCh38#106520611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8697276-A-C

106520611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8697276-A-G

106520662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8697327-G-A

106520721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8697388-G-T

http://identifiers.org/hco/13/GRCh38#106520818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8697493-C-A

106520818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8697493-C-T

http://identifiers.org/hco/13/GRCh38#106520970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8697650-C-A

106520970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8697650-C-G

106521473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8698101-G-A

106521473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 8698101-G-T

106521722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8698313-T-C

106521751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8698342-T-C

106521771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8698362-T-C

106521799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8698391-A-T

106521800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8698392-T-C

106521856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8698453-T-C

106522102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8698739-T-C

http://identifiers.org/hco/13/GRCh38#106522318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8698952-C-A

106522318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8698952-C-T

106522492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8699111-A-G

106522732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8699311-A-G

106523038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8699563-G-A

106523064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8699597-T-A

106523084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8699619-G-C

http://identifiers.org/hco/13/GRCh38#106523206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8699723-A-C

106523206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8699723-A-G

http://identifiers.org/hco/13/GRCh38#106523395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8699834-A-C

106523454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8699883-A-G

106523584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8700022-G-A

106523824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8700259-G-A

106524167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8700569-C-T

106524217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8700621-G-A

http://identifiers.org/hco/13/GRCh38#106524374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8700749-C-A

106524379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8700754-C-T

http://identifiers.org/hco/13/GRCh38#106524438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8700813-A-C

106524476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8700852-T-C

106524576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8700913-C-T

106524832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8701133-G-A

106524998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8701237-T-A

106524998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8701237-T-C

106525607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8701776-G-T

106525770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8701958-C-T

106526153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8702464-G-A

http://identifiers.org/hco/13/GRCh38#106526928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#8703161-C-A

106526928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8703161-C-T

106527428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8703567-C-T

106527734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8703841-C-T

106528296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8704393-C-T

106528445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8704533-T-A

106529081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8705110-G-A

106529152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8705201-A-G

106529184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8705220-A-T

106529626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8705661-C-T

106530191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8706223-C-G

106530191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8706223-C-T

106530197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8706229-A-G

106530733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8706725-G-A

106530976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8706930-C-T

106530983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8706937-T-A

106531046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8706999-C-G

106531409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 8707313-T-C

106532482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8708356-G-A

106532976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8708751-C-T

106533098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron_variant, undefined
orthologous variants: 8708864-A-G

106533503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8709257-G-A

106533516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8709270-A-G

106533612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8709378-C-T

106534332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8710010-C-T

106534547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8710200-G-C

106534796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8710421-G-A

106534796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8710421-G-C

106534796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8710421-G-T

106534820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8710461-G-A

106534820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8710461-G-C

106534820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: intron variant
orthologous variants: 8710461-G-T

106534944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: synonymous variant
orthologous variants: 8710585-G-A

106534944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: synonymous variant
orthologous variants: 8710585-G-C

106534996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5 prime UTR variant
orthologous variants: 8710646-G-A

106534996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5 prime UTR variant
orthologous variants: 8710646-G-T

106535095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5 prime UTR variant
orthologous variants: 8710700-G-A

106535095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5 prime UTR variant
orthologous variants: 8710700-G-T

106535097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5 prime UTR variant
orthologous variants: 8710702-T-A

106535097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5 prime UTR variant
orthologous variants: 8710702-T-G

106535237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5 prime UTR variant
orthologous variants: 8710843-C-T

106535457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5 prime UTR variant
orthologous variants: 8711060-G-C

106535641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3227
most severe consequence: 5 prime UTR variant
orthologous variants: 8711221-G-A