47046206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87666462-T-C

47046223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87666479-T-A

47046223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87666479-T-G

http://identifiers.org/hco/2/GRCh38#47046566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87666789-C-A

47046566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87666789-C-G

http://identifiers.org/hco/2/GRCh38#47046705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87666883-C-A

47046705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87666883-C-T

47046786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87666946-C-T

47046802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87666952-T-G

47046964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667076-T-C

47046981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667091-G-A

47046981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667091-G-T

http://identifiers.org/hco/2/GRCh38#47047214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87667230-C-A

47047281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 87667295-A-G

http://identifiers.org/hco/2/GRCh38#47047360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87667385-C-A

47047360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667385-C-G

http://identifiers.org/hco/2/GRCh38#47047391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87667421-C-A

47047404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667436-G-A

47047404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667436-G-C

47047404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667436-G-T

47047418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667450-G-A

47047418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667450-G-C

47047418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667450-G-T

http://identifiers.org/hco/2/GRCh38#47047433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87667465-C-A

47047487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667512-T-C

http://identifiers.org/hco/2/GRCh38#47047501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87667528-A-C

47047501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667528-A-G

47047595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87667612-A-G

47049209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87668730-G-A

47049872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669233-G-A

47049872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669233-G-T

47050009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669334-G-A

http://identifiers.org/hco/2/GRCh38#47050213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87669402-A-C

47050213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669402-A-G

47050220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669409-G-A

47050220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669409-G-T

http://identifiers.org/hco/2/GRCh38#47050241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87669430-C-A

47050241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669430-C-T

http://identifiers.org/hco/2/GRCh38#47050349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87669552-A-C

47050349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669552-A-T

http://identifiers.org/hco/2/GRCh38#47050413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87669613-C-A

47050513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669707-C-G

47050525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669719-G-A

47050525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669719-G-T

http://identifiers.org/hco/2/GRCh38#47050552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87669746-C-A

http://identifiers.org/hco/2/GRCh38#47050716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87669901-A-C

47050851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669979-T-C

http://identifiers.org/hco/2/GRCh38#47050859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87669987-C-A

47050859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87669987-C-T

47050903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670031-T-C

47050904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670032-G-T

47050909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670037-C-T

47050926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670054-G-T

47050932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670060-A-T

47050973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670095-C-T

http://identifiers.org/hco/2/GRCh38#47050974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87670096-C-A

47050974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670096-C-G

47050974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670096-C-T

47051078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670400-T-A

47051105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670430-A-G

47051116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670441-T-A

47051238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670551-C-T

47051410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670707-A-G

http://identifiers.org/hco/2/GRCh38#47051679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87670832-C-A

47051679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670832-C-G

47051679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87670832-C-T

47051762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 87670900-G-A

47051929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87671085-C-G

47051929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87671085-C-T

47051934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87671090-T-C

http://identifiers.org/hco/2/GRCh38#47051943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87671099-C-A

47051984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87671149-G-A

http://identifiers.org/hco/2/GRCh38#47051994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87671159-C-A

47051994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87671159-C-T

47052108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87671339-G-A

47052270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87671626-G-A

47052270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87671626-G-T

47052494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87671808-T-C

47052506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87671820-C-T

47052674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87671958-C-T

47052714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87671992-G-A

47052873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87672113-G-A

47052880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87672120-T-G

47053036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87672280-C-T

http://identifiers.org/hco/2/GRCh38#47053113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87672361-A-C

47053187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87672437-T-C

47053187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87672437-T-G

47054864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87673050-T-C

47054940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87673111-G-A

47054992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87673156-C-G

http://identifiers.org/hco/2/GRCh38#47055074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87673219-C-A

47055594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87673690-T-C

47055598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87673694-G-A

47055748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87673822-T-C

http://identifiers.org/hco/2/GRCh38#47055943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87673985-C-A

47055943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87673985-C-G

47056035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674103-G-A

47056260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674312-C-G

47056262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674328-G-A

47056409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674592-C-T

http://identifiers.org/hco/2/GRCh38#47056458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87674688-C-A

47056458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674688-C-G

47056461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674691-T-G

http://identifiers.org/hco/2/GRCh38#47056500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87674742-C-A

47056500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674742-C-G

47056562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674806-G-A

47056562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674806-G-T

47056570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674814-G-A

47056719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674970-G-C

47056733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674993-T-C

47056733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87674993-T-G

47056898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87675114-A-G

47057128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87675354-G-A

47057435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87675665-A-G

47057488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87675708-T-A

47057515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87675733-G-A

47057579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87675808-C-T

47057583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87675812-G-A

47057594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87675837-G-A

47057885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676106-C-T

47057924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676146-G-C

47058017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676232-A-G

http://identifiers.org/hco/2/GRCh38#47058048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87676263-C-A

47058048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676263-C-G

47058160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676363-C-G

47058208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676387-T-C

47058216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676390-G-A

47058216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676390-G-T

47058310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676478-C-G

47058344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676502-G-C

47058365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676523-A-G

47058370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676528-C-T

47058594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676729-G-C

47058617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676752-G-C

47058630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676774-C-T

47058851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676991-C-G

47058851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87676991-C-T

47060532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87677697-A-T

http://identifiers.org/hco/2/GRCh38#47060638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87677773-C-A

47060857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 87677975-A-G

47060917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 87678035-G-A

http://identifiers.org/hco/2/GRCh38#47061031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87678138-C-A

47061031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678138-C-T

47061032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678139-G-A

47061032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678139-G-C

47061032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678139-G-T

http://identifiers.org/hco/2/GRCh38#47061041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87678148-C-A

47061041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678148-C-G

47061041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678148-C-T

http://identifiers.org/hco/2/GRCh38#47061065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87678160-C-A

47061065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678160-C-T

http://identifiers.org/hco/2/GRCh38#47061068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87678163-C-A

47061068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678163-C-G

47061068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678163-C-T

47061071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678166-G-A

47061071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678166-G-T

http://identifiers.org/hco/2/GRCh38#47061074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87678169-C-A

47061074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678169-C-T

http://identifiers.org/hco/2/GRCh38#47061085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87678184-C-A

47061085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678184-C-T

http://identifiers.org/hco/2/GRCh38#47061112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87678211-C-A

47061112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678211-C-T

47061223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678329-G-T

47061466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678577-G-C

47061938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87678977-C-T

47062412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87679384-T-C

47062630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87679558-C-G

47062744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87679671-A-G

47062939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87679865-C-T

47062945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87679871-C-T

47062999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87679927-A-G

47062999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87679927-A-T

47063294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87680222-G-T

47063378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87680292-G-A

47063378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87680292-G-T

47063405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87680318-C-T

47067224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87680506-A-G

47067248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87680527-C-G

47067288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87680566-A-G

47067517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87680826-G-A

47067644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87680942-G-A

47067645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87680943-T-G

47067648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87680945-C-T

47067871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681126-T-G

47067920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681178-G-A

47067920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681178-G-T

47068119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681346-G-T

http://identifiers.org/hco/2/GRCh38#47068140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87681367-C-A

47068140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681367-C-G

47068140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681367-C-T

47068141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681368-T-C

47068285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681538-A-G

47068288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681541-G-A

47068288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681541-G-C

47068288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681541-G-T

47068315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681579-G-T

47068318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681581-T-C

47068319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681582-A-T

http://identifiers.org/hco/2/GRCh38#47068338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87681601-C-A

47068338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681601-C-G

47068338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681601-C-T

47068354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681609-G-A

http://identifiers.org/hco/2/GRCh38#47068355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87681610-C-A

47068355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681610-C-T

47068377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87681632-T-C

47069305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87682874-G-T

47069402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87682955-A-G

47069411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87682993-C-T

47069413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87682995-A-T

47069918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87683390-T-A

47069944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87683417-T-A

47069985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87683458-C-T

47070078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87683543-G-A

http://identifiers.org/hco/2/GRCh38#47070172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87683642-A-C

47070276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87683750-C-G

47070277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87683751-C-T

47070278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87683752-C-T

47070281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87683755-T-A

47070393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87683875-G-T

47070576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87684085-A-G

47070845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87684320-C-T

47070981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87684449-G-T

47071097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87684560-G-A

47071097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87684560-G-T

http://identifiers.org/hco/2/GRCh38#47071110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87684573-C-A

47071110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87684573-C-G

47071110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87684573-C-T

47071335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87684804-G-A

47071335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87684804-G-T

47071430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87684895-C-G

http://identifiers.org/hco/2/GRCh38#47071841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87685465-C-A

47071841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87685465-C-T

47071860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87685484-C-T

47071896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87685524-G-A

47072159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87685821-C-G

http://identifiers.org/hco/2/GRCh38#47072224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87685879-A-C

47072226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87685881-G-C

47072226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87685881-G-T

47072280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87685929-C-T

47072284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87685933-T-C

47072286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87685935-T-C

47072613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87686245-G-A

47072730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87686363-T-C

47072738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87686371-C-G

47072780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87686408-C-T

47072784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87686412-C-T

47072862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87686469-G-C

47073199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87686851-G-A

47073319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87686937-C-T

47073522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687121-A-T

47073586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687186-G-A

47073586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687186-G-T

47073603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687200-G-A

47073603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687200-G-C

47073603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687200-G-T

47073681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687256-T-G

47073758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 87687333-T-C

47073758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687333-T-G

47073953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687544-T-C

47074004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687588-G-A

47074004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687588-G-C

47074004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687588-G-T

http://identifiers.org/hco/2/GRCh38#47074005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87687589-C-A

47074088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687715-G-A

47074088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687715-G-T

47074273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87687982-C-G

47074408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688100-A-G

47074446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688133-G-A

47074448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688135-G-A

47074448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688135-G-T

47074456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688142-T-C

47074456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688142-T-G

47074504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688194-A-G

47074513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688203-C-T

47074603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688290-G-A

47074603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688290-G-T

47074609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688327-T-A

47074660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688373-G-T

47074661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688374-C-T

47074801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688542-A-G

http://identifiers.org/hco/2/GRCh38#47074957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87688655-C-A

47074957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688655-C-G

47074957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688655-C-T

47075023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688714-A-T

47075028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688719-T-C

47075047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688738-A-G

47075143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87688815-A-G

47075449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689089-C-T

47075450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689090-A-G

http://identifiers.org/hco/2/GRCh38#47075494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87689130-C-A

47075494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689130-C-G

47075494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689130-C-T

47075556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689190-G-T

47075588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689219-G-A

47075588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689219-G-T

47075634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689260-G-A

47075634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689260-G-T

47075660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689280-A-G

http://identifiers.org/hco/2/GRCh38#47075666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87689286-C-A

47075666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689286-C-G

47075666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689286-C-T

47075696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689298-G-A

47075696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689298-G-C

47075696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689298-G-T

47075737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689331-G-A

47075737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689331-G-T

47075753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689348-A-G

47075766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689362-G-A

47075766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689362-G-T

47075836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689434-G-C

http://identifiers.org/hco/2/GRCh38#47075850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87689453-C-A

47075850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689453-C-G

47075903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689541-A-G

47075905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689543-G-A

47075905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689543-G-C

47075914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689552-A-G

http://identifiers.org/hco/2/GRCh38#47075935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87689585-C-A

47075935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689585-C-T

47075980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689660-G-A

47075980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87689660-G-T

http://identifiers.org/hco/2/GRCh38#47076126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87689831-C-A

http://identifiers.org/hco/2/GRCh38#47076147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87689852-C-A

47076160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87689862-T-C

http://identifiers.org/hco/2/GRCh38#47076185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87689888-C-A

47076185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87689888-C-G

47076197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87689900-G-T

47076223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87689929-C-G

47076223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87689929-C-T

47076246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87689952-G-T

47076291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87689976-G-A

47076628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87690487-C-T

47076666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87690518-A-G

47076692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87690541-C-T

47076745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87690590-T-A

http://identifiers.org/hco/2/GRCh38#47076866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#87690703-C-A

47076916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87690757-C-T

47077195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87691018-A-G

47077195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87691018-A-T

47077210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691033-T-A

47077343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691138-C-G

47077886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691504-G-T

47077899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691517-T-C

47078082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691662-C-G

47078185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691744-T-C

47078202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691761-G-C

47078203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691762-A-G

http://identifiers.org/hco/2/GRCh38#47078208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87691767-A-C

47078212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691771-G-A

47078216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691775-T-C

47078335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691873-G-A

47078360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691899-C-T

47078361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87691901-G-A

47078670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87692192-G-A

47085612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87693456-G-C

47086343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87694901-G-A

47086828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87696893-A-T

47086937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87696952-T-A

47086937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87696952-T-C

47086939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87696954-G-A

47086939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87696954-G-T

http://identifiers.org/hco/2/GRCh38#47086943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87696958-A-C

47086961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87696974-A-G

47086961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87696974-A-T

47087194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87697195-G-A

47087194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87697195-G-C

47087194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87697195-G-T

47087205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87697206-G-A

47087205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87697206-G-T

47087216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87697217-G-A

http://identifiers.org/hco/2/GRCh38#47087223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87697224-A-C

http://identifiers.org/hco/2/GRCh38#47087376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87697331-C-A

47087473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87697428-C-T

47087717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

http://identifiers.org/hco/2/GRCh38#47088686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87698754-A-C

47088836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87698923-C-G

47088864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87698951-G-C

http://identifiers.org/hco/2/GRCh38#47090015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87702133-C-A

47090019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702137-C-T

47090043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702161-G-A

47090043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702161-G-C

47090177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702505-A-G

47090177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702505-A-T

47090182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702511-G-A

47090182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702511-G-C

47090182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702511-G-T

47090187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702517-T-C

47090224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702553-C-T

47090227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702556-T-C

http://identifiers.org/hco/2/GRCh38#47090229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87702558-C-A

47090229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702558-C-G

47090290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 87702609-G-A

47090290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 87702609-G-C

47090290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 87702609-G-T

47090418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702744-G-T

47090486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702809-T-C

47090486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702809-T-G

47090495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702818-T-A

47090495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702818-T-C

47090518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702839-G-A

47090561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87702885-C-T

http://identifiers.org/hco/2/GRCh38#47094370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87703443-C-A

47094376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87703450-C-T

47094377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87703451-A-G

47094450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87703528-G-A

47094450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87703528-G-C

47094507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87703564-G-A

47095013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87703853-G-A

47095049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87703875-A-G

47095049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87703875-A-T

47095477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704316-C-T

47095513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704335-G-A

47095642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704462-C-G

47095648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704468-C-T

47095649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704469-A-G

47095651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704471-G-A

47095742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704551-C-G

47095742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704551-C-T

http://identifiers.org/hco/2/GRCh38#47095744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87704553-C-A

47095744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704553-C-G

47095744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704553-C-T

47095745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704554-A-G

47095793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704604-G-C

47095804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704615-A-G

47095815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704626-T-C

47095860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704668-G-A

47095898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704703-C-T

47095974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704866-C-G

47096046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87704969-A-G

47096082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87705000-T-C

47096099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87705017-T-C

47096301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87705180-G-C

http://identifiers.org/hco/2/GRCh38#47096312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87705191-C-A

47096340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87705267-G-A

47096411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87705346-G-A

47096443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87705374-G-A

47109718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87706776-T-C

47109743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87706801-T-C

47109773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87706831-G-T

http://identifiers.org/hco/2/GRCh38#47109788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87706846-A-C

47109802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87706860-T-C

47109865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87706928-T-A

47109936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87706979-C-T

47109954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87706997-C-T

47109965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87707009-T-C

47112610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87709971-G-C

47112702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87710057-G-C

http://identifiers.org/hco/2/GRCh38#47112723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87710083-C-A

47112756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87710120-A-G

47113208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87710832-C-T

47115975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87714779-T-C

47118640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87715368-T-A

47118901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87715581-C-T

47119047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, undefined
orthologous variants: 87715721-G-A

47119252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87715963-G-A

47119298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, undefined
orthologous variants: 87716008-G-A

47119308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87716018-A-T

47119341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron_variant, undefined
orthologous variants: 87716064-G-C

http://identifiers.org/hco/2/GRCh38#47119440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87716153-C-A

47130030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87718756-T-A

47130122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87718863-G-C

47130122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87718863-G-T

47130168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87718913-G-A

47130168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87718913-G-C

47130290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87719042-A-G

http://identifiers.org/hco/2/GRCh38#47142294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87723619-C-A

47142294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87723619-C-T

47145117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87725363-G-A

47145227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87725477-C-G

47145411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87725665-T-C

47145423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87725677-G-A

47145594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87725867-G-A

47145622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87725898-T-C

47149152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87727398-A-G

47149593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87727791-T-C

47151101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87728795-C-T

http://identifiers.org/hco/2/GRCh38#47151158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87729812-C-A

47151158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87729812-C-T

47151186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87729874-C-T

47151203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87729891-C-T

47151340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: missense variant
orthologous variants: 87730024-T-A

47151340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: missense variant
orthologous variants: 87730024-T-C

47151360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: synonymous variant
orthologous variants: 87730044-A-G

47151390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: synonymous variant
orthologous variants: 87730074-G-A

47151390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: missense variant
orthologous variants: 87730074-G-C

47151426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: synonymous variant
orthologous variants: 87730110-G-A

47151475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: missense variant
orthologous variants: 87730159-A-G

47151486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: missense variant
orthologous variants: 87730170-C-G

47151486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: synonymous variant
orthologous variants: 87730170-C-T

47151507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: synonymous variant
orthologous variants: 87730191-A-G

47151635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87730298-A-G

47152400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87731925-G-C

47152566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87732073-T-C

47152705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87732808-T-C

http://identifiers.org/hco/2/GRCh38#47152849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87732962-C-A

47152851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87732964-A-G

http://identifiers.org/hco/2/GRCh38#47152855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87732968-C-A

47152855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87732968-C-T

47152872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87732985-A-T

http://identifiers.org/hco/2/GRCh38#47152889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87733004-C-A

47152889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87733004-C-T

47152925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87733039-T-C

47152941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87733056-T-C

47153000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: missense variant
orthologous variants: 87733114-G-A

http://identifiers.org/hco/2/GRCh38#47153112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87733210-C-A

47153125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87733230-T-C

47153141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87733246-T-A

http://identifiers.org/hco/2/GRCh38#47153991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87734115-C-A

47154219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734317-T-C

http://identifiers.org/hco/2/GRCh38#47154280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87734400-A-C

47154285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734405-T-C

47154309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734427-C-G

47154436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734542-T-C

http://identifiers.org/hco/2/GRCh38#47154581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87734686-A-C

47154694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734722-G-A

47154739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734737-A-G

47154897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734781-T-A

47155026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734884-G-A

47155026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734884-G-C

47155026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734884-G-T

47155032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734890-T-C

http://identifiers.org/hco/2/GRCh38#47155082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#87734927-A-C

47155082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734927-A-G

47155102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734947-G-A

47155102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734947-G-C

47155102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734947-G-T

47155118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734958-T-A

47155118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734958-T-C

47155118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: intron variant
orthologous variants: 87734958-T-G

47155271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26850
most severe consequence: 5 prime UTR variant
orthologous variants: 87735111-A-G