27582982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: 31609756-G-A

27582982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: 31609756-G-T

27582984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: 31609758-T-C

27582984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: 31609758-T-G

27583000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: 31609774-A-T

27583011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: 31609785-A-G

27583012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: 31609786-G-A

http://identifiers.org/hco/2/GRCh38#27583015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31609789-C-A

27583015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: 31609789-C-G

http://identifiers.org/hco/2/GRCh38#27583023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31609797-A-C

27583023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: 31609797-A-G

27583023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: 31609797-A-T

27583039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5 prime UTR variant
orthologous variants: 31609813-G-C

27583052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31609831-G-T

http://identifiers.org/hco/2/GRCh38#27583060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31609839-C-A

27583060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31609839-C-G

27583060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31609839-C-T

27583068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31609847-T-A

27583068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31609847-T-C

27583070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31609849-G-C

27583070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31609849-G-T

http://identifiers.org/hco/2/GRCh38#27583072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31609851-C-A

27583072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31609851-C-G

27583072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31609851-C-T

27583084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31609863-G-A

27583138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31609917-C-T

27583140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 31609919-G-A

27583140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 31609919-G-T

27583142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 31609921-C-T

27583147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31609926-G-A

27583151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31609930-C-T

27583188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31609967-G-C

27583310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610107-G-A

27583310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610107-G-T

http://identifiers.org/hco/2/GRCh38#27583312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31610109-C-A

27583312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610109-C-G

27583312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610109-C-T

27583315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610112-T-C

http://identifiers.org/hco/2/GRCh38#27583321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31610118-A-C

27583321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610118-A-G

27583321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610118-A-T

27583329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610126-G-A

27583329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610126-G-C

27583330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610127-G-A

27583330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610127-G-T

27583334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610131-T-A

27583334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610131-T-C

http://identifiers.org/hco/2/GRCh38#27583339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31610136-C-A

http://identifiers.org/hco/2/GRCh38#27583345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31610142-C-A

http://identifiers.org/hco/2/GRCh38#27583347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31610144-C-A

27583347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610144-C-T

27583399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610235-T-C

http://identifiers.org/hco/2/GRCh38#27583429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31610271-C-A

http://identifiers.org/hco/2/GRCh38#27583481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31610324-C-A

27583481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610324-C-T

27583495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610338-T-C

27583496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610339-G-C

27583532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610375-G-T

27583537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610381-C-T

27583554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610398-T-A

27583560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610403-G-A

27583560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610403-G-C

27583568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610411-T-C

27583568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610411-T-G

http://identifiers.org/hco/2/GRCh38#27583591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31610432-A-C

27583605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610446-T-C

27583635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610476-C-G

27583638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610479-G-A

http://identifiers.org/hco/2/GRCh38#27583662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#31610503-C-A

27583662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610503-C-G

27583662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610503-C-T

27583694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 31610535-A-G

27583735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610576-G-A

27583749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610591-T-G

http://identifiers.org/hco/2/GRCh38#27583757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31610599-C-A

27583791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610611-A-G

27583793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610613-A-G

27583811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610631-G-A

27583811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610631-G-T

27583836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610656-G-A

27583836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610656-G-C

27583836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610656-G-T

http://identifiers.org/hco/2/GRCh38#27583850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31610670-C-A

27583850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610670-C-T

27583856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610676-A-G

27583860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610680-G-T

27584077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610720-A-G

27584125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610763-G-A

27584191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610830-A-G

27584301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31610945-A-G

27584426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31611069-A-G

27584479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31611124-C-T

27584830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31611987-A-G

27584831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31611988-G-A

27584831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31611988-G-C

27584865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31612012-C-T

27584866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31612013-G-A

27584871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31612018-G-A

27585764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31613838-C-T

27586193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31614274-G-T

27586355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31614446-G-A

27586521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31614655-C-T

27586542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31614678-C-G

27597946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31622579-G-T

27598158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31622881-T-G

27598184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31622907-A-T

27598204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31622927-A-G

27598204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31622927-A-T

27598258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31622981-T-G

27598333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31623061-A-G

27598496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31623249-G-T

27598502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31623255-G-A

http://identifiers.org/hco/2/GRCh38#27598610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31623351-A-C

27598630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31623371-A-G

27599452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31623459-T-C

http://identifiers.org/hco/2/GRCh38#27599523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31623529-C-A

27599523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31623529-C-T

27599575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31623568-T-A

http://identifiers.org/hco/2/GRCh38#27599645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31623647-C-A

27599645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31623647-C-G

27599645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 31623647-C-T

http://identifiers.org/hco/2/GRCh38#27599723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31623711-C-A

27599753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31623739-G-A

http://identifiers.org/hco/2/GRCh38#27599819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31623804-C-A

27599819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31623804-C-T

27599832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31623817-A-G

27599832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31623817-A-T

27599886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31623877-A-G

27599891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31623882-G-A

27600007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31623973-A-G

27600018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31623984-G-A

27600018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31623984-G-C

http://identifiers.org/hco/2/GRCh38#27600096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31624097-C-A

http://identifiers.org/hco/2/GRCh38#27600165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31624173-C-A

http://identifiers.org/hco/2/GRCh38#27600190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31624199-C-A

27600190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31624199-C-G

27600209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31624221-T-C

27600482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31624476-T-A

http://identifiers.org/hco/2/GRCh38#27600572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31624566-C-A

27600572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31624566-C-T

27600687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31624662-G-C

27600687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 31624662-G-T

http://identifiers.org/hco/2/GRCh38#27600950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31624920-C-A

27600950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31624920-C-G

27600950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31624920-C-T

http://identifiers.org/hco/2/GRCh38#27602156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31627413-A-C

27602163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31627425-C-T

http://identifiers.org/hco/2/GRCh38#27602241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31627507-A-C

27602241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31627507-A-G

27602354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31627603-G-A

27602354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31627603-G-T

27602356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31627605-A-G

http://identifiers.org/hco/2/GRCh38#27602358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31627607-C-A

27602358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31627607-C-T

27602526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: synonymous variant
orthologous variants: 31627765-C-T

http://identifiers.org/hco/2/GRCh38#27602800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31628040-C-A

27602800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31628040-C-G

27602800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31628040-C-T

27602994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31628208-G-A

27602994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31628208-G-T

27603032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31628241-A-G

27603032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31628241-A-T

27603121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31628322-G-C

27603256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: synonymous variant
orthologous variants: 31628457-A-G

27603261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: missense variant
orthologous variants: 31628462-G-A

27603343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31628540-A-G

27607825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31630096-G-C

27607825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31630096-G-T

27615129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31630761-T-A

27615129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31630761-T-C

27615306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31630932-A-G

27615448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31631053-G-A

27615600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31631190-C-T

27615626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31631217-G-A

27616134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31632892-G-A

27616134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31632892-G-C

27616134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31632892-G-T

http://identifiers.org/hco/2/GRCh38#27616147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31632905-C-A

27616147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31632905-C-T

27616173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31632931-A-G

27616441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31633194-G-A

http://identifiers.org/hco/2/GRCh38#27616463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31633216-A-C

27616746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31633470-C-T

27616940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron variant
orthologous variants: 31633678-G-T

27617092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31633807-G-T

27617093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31633808-G-A

http://identifiers.org/hco/2/GRCh38#27617163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31633875-C-A

27617163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31633875-C-G

27617163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31633875-C-T

http://identifiers.org/hco/2/GRCh38#27617340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31634020-A-C

27617340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31634020-A-G

27617502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31634154-T-C

27617520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31634172-A-G

27617535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31634187-T-A

27617535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31634187-T-C

27617607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31634274-A-G

27617706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31634360-T-C

http://identifiers.org/hco/2/GRCh38#27617707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31634361-C-A

http://identifiers.org/hco/2/GRCh38#27621035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31637198-C-A

27621035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31637198-C-G

27621035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31637198-C-T

http://identifiers.org/hco/2/GRCh38#27621059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31637223-C-A

27621059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31637223-C-T

27621218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31637379-G-A

27621273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31637434-A-T

http://identifiers.org/hco/2/GRCh38#27621302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31637463-C-A

27621302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31637463-C-G

27621302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31637463-C-T

27621343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31637504-G-A

27621384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31637524-C-G

27621384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31637524-C-T

27621386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 31637526-A-G

27621425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 31637565-G-C

27621560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31637703-T-C

27621569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31637712-G-A

27621569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31637712-G-T

27621596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31637732-G-A

27621596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31637732-G-T

27621696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31637822-G-A

27621696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31637822-G-T

http://identifiers.org/hco/2/GRCh38#27621747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31637872-A-C

27621747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31637872-A-T

27621752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31637877-T-A

27621752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31637877-T-C

27621752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31637877-T-G

http://identifiers.org/hco/2/GRCh38#27621794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31637926-A-C

27621812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31637944-T-C

http://identifiers.org/hco/2/GRCh38#27621878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31638013-A-C

http://identifiers.org/hco/2/GRCh38#27621979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#31638112-A-C

27621985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31638118-G-T

27621992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31638125-G-T

27622128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31638240-A-G

27622171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31638283-G-A

27622370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31638380-T-C

27622765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31638764-C-T

27622935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 31638941-G-T

27622996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 31639008-G-T

27623131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 31639132-T-A

27623180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 31639179-G-T

27623184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 31639183-T-G

27623204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29380
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 31639186-A-G