47709773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97608935-C-T

47709804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97608967-T-A

47709837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97608997-G-A

47709837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97608997-G-T

http://identifiers.org/hco/12/GRCh38#47710056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97609230-C-A

http://identifiers.org/hco/12/GRCh38#47710113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97609287-C-A

http://identifiers.org/hco/12/GRCh38#47710151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97609321-C-A

47710151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609321-C-T

47710172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609342-T-C

http://identifiers.org/hco/12/GRCh38#47710382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97609505-C-A

47710401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609527-T-A

47710401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609527-T-C

47710401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609527-T-G

47710469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609594-A-G

47710469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609594-A-T

47710473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609598-G-T

http://identifiers.org/hco/12/GRCh38#47710574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97609688-C-A

47710574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609688-C-T

47710636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609763-A-T

47710674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609801-A-G

http://identifiers.org/hco/12/GRCh38#47710714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97609839-C-A

47710714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609839-C-T

http://identifiers.org/hco/12/GRCh38#47710734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97609859-C-A

47710734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97609859-C-G

47710853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97609984-A-G

47710947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610082-G-T

47710958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610093-T-G

http://identifiers.org/hco/12/GRCh38#47710964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97610098-C-A

47710964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610098-C-G

http://identifiers.org/hco/12/GRCh38#47710970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97610104-C-A

47710970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610104-C-G

47710970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610104-C-T

47710977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610112-G-A

47710977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610112-G-T

http://identifiers.org/hco/12/GRCh38#47711012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97610145-C-A

47711012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610145-C-G

47711012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610145-C-T

http://identifiers.org/hco/12/GRCh38#47711079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97610194-C-A

47711251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610379-C-T

47711256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610384-G-A

http://identifiers.org/hco/12/GRCh38#47711528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97610745-C-A

47711528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610745-C-T

47711545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610750-G-T

47711563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610768-T-C

47711580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610785-A-G

47711589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610794-T-C

http://identifiers.org/hco/12/GRCh38#47711596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97610801-C-A

47711596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97610801-C-T

47711643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97610849-G-A

47711677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97610883-C-G

47711677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97610883-C-T

47711692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97610898-G-C

47711869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97611053-A-G

http://identifiers.org/hco/12/GRCh38#47712084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97611235-A-C

47712220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97611367-G-A

47712299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97611462-T-C

47712432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97611577-T-C

47712447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97611593-C-T

47712464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97611610-T-C

47712464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97611610-T-G

http://identifiers.org/hco/12/GRCh38#47712516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97611662-A-C

47712525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97611671-G-A

47712546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97611692-A-G

http://identifiers.org/hco/12/GRCh38#47712669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97611819-C-A

47712669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97611819-C-G

http://identifiers.org/hco/12/GRCh38#47712672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97611822-C-A

47712698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97611851-T-A

47712698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97611851-T-G

http://identifiers.org/hco/12/GRCh38#47712701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97611854-C-A

47712701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97611854-C-T

47712735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97611902-G-T

47712960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612101-C-T

47713167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612276-T-A

47713167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612276-T-G

47713168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612277-A-T

http://identifiers.org/hco/12/GRCh38#47713179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97612288-C-A

47713179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612288-C-G

47713179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612288-C-T

http://identifiers.org/hco/12/GRCh38#47713213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97612322-C-A

47713213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612322-C-T

47713215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612324-T-C

47713236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612339-A-G

47713363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97612465-A-G

47713440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612542-G-A

http://identifiers.org/hco/12/GRCh38#47713508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97612594-C-A

47713508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612594-C-G

47713508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612594-C-T

http://identifiers.org/hco/12/GRCh38#47713511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97612597-A-C

http://identifiers.org/hco/12/GRCh38#47713521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97612607-C-A

47713606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612722-G-A

47713609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612725-A-G

47713714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612825-C-T

47713753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612871-T-A

47713753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612871-T-C

47713753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612871-T-G

47713803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612926-C-G

47713803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612926-C-T

47713805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97612928-G-A

47713917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97613066-G-T

http://identifiers.org/hco/12/GRCh38#47714733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

47715085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-T

47715613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616039-G-A

47715698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616124-A-G

http://identifiers.org/hco/12/GRCh38#47715860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97616275-C-A

47715860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616275-C-G

http://identifiers.org/hco/12/GRCh38#47715959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97616325-A-C

47715984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616350-T-C

47715984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616350-T-G

47716052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616401-G-A

47716106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616454-G-T

http://identifiers.org/hco/12/GRCh38#47716213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97616534-C-A

47716213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616534-C-G

47716249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616585-G-C

47716249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616585-G-T

http://identifiers.org/hco/12/GRCh38#47716264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97616600-A-C

http://identifiers.org/hco/12/GRCh38#47716382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97616724-C-A

47716382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97616724-C-T

47716476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97616818-T-C

47716476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97616818-T-G

http://identifiers.org/hco/12/GRCh38#47716487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#97616829-A-C

47716487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97616829-A-G

47716487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 97616829-A-T

47716505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97616847-G-A

47716525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616865-C-T

47716529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616869-G-A

47716529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616869-G-C

47716531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97616871-G-T

http://identifiers.org/hco/12/GRCh38#47716536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97616876-A-C

47716820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617341-T-C

http://identifiers.org/hco/12/GRCh38#47716825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97617346-A-C

47716825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617346-A-G

47716825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617346-A-T

http://identifiers.org/hco/12/GRCh38#47716827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97617348-A-C

47716827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617348-A-G

47716841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617362-G-A

47716841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617362-G-T

47717006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97617511-A-G

47717036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97617541-G-A

47717115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617624-G-A

47717132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617646-C-T

47717161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617675-G-A

47717161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617675-G-T

47717174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617687-G-T

http://identifiers.org/hco/12/GRCh38#47717182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97617695-A-C

47717249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617758-T-G

47717323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617839-G-A

47717374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617882-T-C

47717439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617927-G-C

47717439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97617927-G-T

47717577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97618063-G-A

47717577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97618063-G-T

47717624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 97618110-G-A

47717637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 97618123-G-A

47717637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 97618123-G-C

http://identifiers.org/hco/12/GRCh38#47717789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97618278-C-A

http://identifiers.org/hco/12/GRCh38#47717802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97618292-C-A

47717802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97618292-C-T

47717871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97618362-T-C

http://identifiers.org/hco/12/GRCh38#47717933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97618422-C-A

47717933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618422-C-T

47717951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97618435-C-G

47717951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97618435-C-T

http://identifiers.org/hco/12/GRCh38#47717952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#97618436-C-A

47717952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97618436-C-G

47717952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97618436-C-T

47717953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97618437-C-T

http://identifiers.org/hco/12/GRCh38#47717959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97618443-C-A

47717959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618443-C-T

http://identifiers.org/hco/12/GRCh38#47717972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97618456-C-A

47717972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618456-C-G

47717972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618456-C-T

http://identifiers.org/hco/12/GRCh38#47717988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97618472-C-A

47717988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618472-C-T

47718047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618517-A-T

http://identifiers.org/hco/12/GRCh38#47718153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#97618594-C-A

47718153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97618594-C-T

http://identifiers.org/hco/12/GRCh38#47718177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#97618618-C-A

47718177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97618618-C-G

47718225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618669-A-G

47718225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618669-A-T

http://identifiers.org/hco/12/GRCh38#47718242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97618686-C-A

47718242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618686-C-T

47718257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618701-T-C

47718284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618725-G-A

47718284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618725-G-C

47718284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618725-G-T

47718285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618726-A-G

47718293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618734-G-A

47718293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618734-G-T

47718315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618755-A-G

http://identifiers.org/hco/12/GRCh38#47718316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97618756-C-A

47718316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618756-C-T

47718335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618763-G-A

47718401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97618832-A-G

47718584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97621807-T-G

47718811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97621974-G-T

47718821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97621984-A-G

47718893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97622042-C-T

47718968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97622124-A-G

47718986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97622143-C-G

47719059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97622213-T-C

47719191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 97622342-G-T

47719259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97622404-G-A

47719259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97622404-G-T

47719261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97622406-G-T

47719285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97622433-G-T

47719286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97622434-G-T

47719344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97622494-T-C

47719364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97622520-G-T

http://identifiers.org/hco/12/GRCh38#47720349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97623961-C-A

http://identifiers.org/hco/12/GRCh38#47720468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97624075-C-A

47720468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97624075-C-T

http://identifiers.org/hco/12/GRCh38#47720549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97624165-C-A

http://identifiers.org/hco/12/GRCh38#47720633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97624260-C-A

47720633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97624260-C-T

47720687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97624315-C-T

47720862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97624497-G-C

47720946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97624581-G-A

47720947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97624582-G-C

47720947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97624582-G-T

47721134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97624749-A-G

47721697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97625208-G-A

47721819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97625568-T-C

http://identifiers.org/hco/12/GRCh38#47721971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97625854-A-C

47722364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97626187-A-G

47722428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97626254-G-T

47722429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97626255-G-T

http://identifiers.org/hco/12/GRCh38#47722678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97626499-C-A

http://identifiers.org/hco/12/GRCh38#47722878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97626721-A-C

47723134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97626989-G-A

47723215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97627070-T-C

47723930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97627797-T-G

47724163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97628004-T-C

47724247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97628095-C-T

47724423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97628281-C-T

47724440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97628298-C-T

47724519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97628365-A-G

47724766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97628598-A-G

47724879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97628721-G-A

47724887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97628729-C-G

http://identifiers.org/hco/12/GRCh38#47724942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97628751-C-A

47724992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97628804-C-T

47725209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97628985-G-A

47725209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97628985-G-C

47725209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97628985-G-T

47725244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97629018-A-G

47725267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97629041-G-T

47725321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97629064-C-T

47725335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97629072-C-G

47725383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97629120-C-G

47725383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97629120-C-T

47725393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97629130-C-T

http://identifiers.org/hco/12/GRCh38#47725504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14369
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#97629234-C-A