92770637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883157-A-G

92770657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883137-G-C

92770657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95883137-G-T

http://identifiers.org/hco/12/GRCh38#92770818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95882971-A-C

http://identifiers.org/hco/12/GRCh38#92770980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95882846-C-A

92770992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95882834-G-T

92771013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95882828-G-A

92771554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95882235-A-T

92771689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95882102-A-G

http://identifiers.org/hco/12/GRCh38#92772223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95881668-A-C

92772306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 95881574-T-C

http://identifiers.org/hco/12/GRCh38#92772415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95881463-A-C

http://identifiers.org/hco/12/GRCh38#92772786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95881090-C-A

92772786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: 95881090-C-T

http://identifiers.org/hco/12/GRCh38#92772820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95881056-C-A

92773527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: 95880353-G-A

92773560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: 95880321-T-C

92773885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: 95879985-G-A

92773885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: 95879985-G-T

92773907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: 95879963-T-A

92774272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: 95879639-G-T

http://identifiers.org/hco/12/GRCh38#92774490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95879409-A-C

92774964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: 95878987-A-G

92774987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: 95878963-T-C

http://identifiers.org/hco/12/GRCh38#92775396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95878622-A-C

92775529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: 95878498-T-G

92775883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: 95878162-T-C

92775895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3 prime UTR variant
orthologous variants: 95878150-T-C

92776078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95877997-G-C

92776078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95877997-G-T

http://identifiers.org/hco/12/GRCh38#92776198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95877878-C-A

92776198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95877878-C-T

92776309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95877800-A-G

http://identifiers.org/hco/12/GRCh38#92776500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95877617-A-C

http://identifiers.org/hco/12/GRCh38#92776698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95877436-C-A

92777239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95876996-T-C

92777263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95876783-T-C

http://identifiers.org/hco/12/GRCh38#92777398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95876657-C-A

92777398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95876657-C-T

92777423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95876440-A-G

92777580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95876195-G-A

92777733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95876041-A-T

92777760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 95876016-T-C

http://identifiers.org/hco/12/GRCh38#92777817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95875960-C-A

92777817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95875960-C-G

92777817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 95875960-C-T

92778287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95875272-G-A

92778310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95875251-A-G

92778402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95875155-T-C

92778446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95875118-C-T

92779129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95874724-T-C

92779272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95874581-T-C

92779295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95874558-T-C

http://identifiers.org/hco/12/GRCh38#92780227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95873459-C-A

92780249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95873436-G-T

92780311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95873374-T-C

92780311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95873374-T-G

92780553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95873163-G-A

92780553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95873163-G-C

92780561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95873155-G-A

92780561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95873155-G-T

92780712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95873074-A-G

92782074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95872501-C-G

92782158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95872415-A-G

92782211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95872369-C-T

http://identifiers.org/hco/12/GRCh38#92782625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95871660-A-C

92784267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95870696-G-A

92784267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95870696-G-C

92784331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95870649-G-C

92784664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95870227-T-C

92784692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95870199-C-T

92784794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95870164-C-T

92785150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron_variant, undefined
orthologous variants: 95869866-T-G

92785328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron_variant, undefined
orthologous variants: 95869682-G-A

92786663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95868723-A-G

92786878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95868426-A-T

92787240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95868114-C-T

92787731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95867670-A-G

92787731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95867670-A-T

92787844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95867576-T-C

92787844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95867576-T-G

92788053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 95867367-A-T

92788066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95867355-T-C

92788166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95867261-G-C

92788166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95867261-G-T

92788320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95867108-G-A

92788320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95867108-G-C

92788480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95866960-A-G

92798797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95864527-C-T

92799108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95864233-T-C

92799127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95864215-T-A

92799127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95864215-T-C

92801268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95863618-G-A

92801268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95863618-G-T

http://identifiers.org/hco/12/GRCh38#92801555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95863057-C-A

92801555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95863057-C-T

http://identifiers.org/hco/12/GRCh38#92801588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95863025-A-C

92801588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron variant
orthologous variants: 95863025-A-G

http://identifiers.org/hco/12/GRCh38#92801592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95863021-A-C

92801613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95863000-T-C

92802498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95862653-T-C

92802515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: synonymous variant
orthologous variants: 95862636-T-C

92802525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95862626-G-A

92802558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: missense variant
orthologous variants: 95862593-G-A

92802756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95862398-T-G

92802758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95862396-T-C

92802871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95862294-A-G

http://identifiers.org/hco/12/GRCh38#92809022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95862026-C-A

92809022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 95862026-C-T

92809034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 95862014-A-G

92809113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95861935-T-C

92809177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95861876-G-A

92809177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95861876-G-T

http://identifiers.org/hco/12/GRCh38#92809817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95861578-C-A

92809817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95861578-C-T

92809978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95861417-T-C

92810822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95860326-A-G

http://identifiers.org/hco/12/GRCh38#92811027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95860143-A-C

92811127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95860055-G-A

92811127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95860055-G-C

92811127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95860055-G-T

92811162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95860024-T-C

92811162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95860024-T-G

92811195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95859994-A-G

92811220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95859969-G-T

http://identifiers.org/hco/12/GRCh38#92811227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95859962-C-A

92811227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95859962-C-T

92811233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95859956-T-C

92811237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95859952-G-A

92811237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95859952-G-C

92811237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95859952-G-T

92811247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95859943-A-G

92811248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95859942-T-C

92811540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95859666-T-A

92811540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95859666-T-C

92812958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95857602-G-A

92812958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95857602-G-T

92812969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95857591-T-C

http://identifiers.org/hco/12/GRCh38#92813001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95857559-A-C

92813197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95857370-G-A

92813197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95857370-G-C

92813197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95857370-G-T

92813367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95857120-C-T

http://identifiers.org/hco/12/GRCh38#92813456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95857006-A-C

http://identifiers.org/hco/12/GRCh38#92813513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95856956-C-A

92814617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95856280-A-G

92814836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95856067-T-C

92816354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95855737-T-G

92816425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95855664-T-C

92816430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95855659-T-C

92816495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95855596-T-A

92816510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95855581-T-A

92816679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95855404-T-G

92817182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95855063-T-A

92817224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95855039-T-C

92819117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95854242-C-T

92819227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95854145-G-T

92819288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95854089-A-G

92819450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95853927-T-C

http://identifiers.org/hco/12/GRCh38#92819992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95853423-C-A

http://identifiers.org/hco/12/GRCh38#92821055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95852053-C-A

http://identifiers.org/hco/12/GRCh38#92821170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95851935-C-A

92821524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95851605-C-T

92823988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95851379-T-A

92824064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95851320-C-G

92824067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95851317-A-G

92825452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95850078-T-A

92825452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95850078-T-C

92825618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95849912-C-T

92825635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95849897-T-C

http://identifiers.org/hco/12/GRCh38#92826021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95849370-C-A

92826021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95849370-C-T

92826067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95849324-G-A

92826067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95849324-G-T

92826072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95849319-T-A

92826072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95849319-T-C

92826072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95849319-T-G

92826190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 95849261-G-A

92826190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 95849261-G-T

92826191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95849260-G-A

92826810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95848953-T-G

92826867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95848886-G-A

92826919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95848838-C-T

92826954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95848807-A-T

92827610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95848404-T-G

92827877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95848146-T-C

92827900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95848106-A-G

92827993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 95848013-T-C

92828053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 95847953-G-A

92828053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95847953-G-C

92828053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95847953-G-T

http://identifiers.org/hco/12/GRCh38#92828118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#95847900-A-C

92828292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95847732-T-C

92828325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95847639-C-T

92832752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 95846733-G-A

92832752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 95846733-G-C

92832901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95846588-T-C

92833236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95846277-G-A

92833264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95846258-C-G

92835369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95839861-T-G

92835400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95839832-C-T

92841912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95839416-T-A

92842361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95838961-T-A

92842361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95838961-T-G

92842445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95838883-T-C

http://identifiers.org/hco/12/GRCh38#92842601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95838733-C-A

92842601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95838733-C-T

92842644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95838712-G-A

92842644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95838712-G-C

92842644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95838712-G-T

92842898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95838439-C-T

92843570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95838106-G-A

92845623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95837240-A-G

92846134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95836349-G-T

92849287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95834402-T-C

http://identifiers.org/hco/12/GRCh38#92849419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95834291-C-A

92849419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95834291-C-T

92849624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95833970-T-C

92849731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95833895-T-C

92849775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95833850-A-G

http://identifiers.org/hco/12/GRCh38#92850833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95833038-C-A

92851322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95832740-A-T

http://identifiers.org/hco/12/GRCh38#92851394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95832670-C-A

92851768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95832238-G-A

92851772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95832234-T-A

92851772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95832234-T-C

92852022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95831794-C-T

92852402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95831314-T-C

92852520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95831234-A-G

92853770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95829451-G-T

92853790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95829429-C-T

http://identifiers.org/hco/12/GRCh38#92853837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95829386-A-C

92853837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95829386-A-G

92853920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 95829318-G-A

92853920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 95829318-G-T

92854013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95829226-A-G

92854090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95829173-G-A

92854090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95829173-G-T

92854093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95829170-G-A

92854093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95829170-G-T

92854545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95828937-G-A

http://identifiers.org/hco/12/GRCh38#92857136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95826479-C-A

http://identifiers.org/hco/12/GRCh38#92857415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95826185-C-A

92857415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 95826185-C-T

92857558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95826056-G-A

92857558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95826056-G-T

92864728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95825683-T-A

92864728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95825683-T-C

92864728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95825683-T-G

92865031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95825380-T-C

92866345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95823147-C-G

92866564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95822947-A-G

92867925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95817102-C-G

92867962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95817060-G-A

92867985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95817037-A-G

http://identifiers.org/hco/12/GRCh38#92867991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95817029-A-C

http://identifiers.org/hco/12/GRCh38#92868053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95816954-A-C

92868057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95816950-A-G

92868074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95816933-G-C

92868074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95816933-G-T

92868078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95816929-A-G

92868541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95816194-A-G

92868847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95815929-G-C

92868912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95815874-G-C

92869237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95815608-A-T

http://identifiers.org/hco/12/GRCh38#92870282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95815062-A-C

92870454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95814901-C-T

http://identifiers.org/hco/12/GRCh38#92871029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95814500-A-C

92871108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95814439-C-T

http://identifiers.org/hco/12/GRCh38#92871154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95814396-A-C

92871154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95814396-A-G

92871154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95814396-A-T

92871286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95814267-C-T

92871575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95813993-T-C

92871802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95813311-T-C

92872660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95812678-A-G

92891075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95810346-T-A

92891260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95810233-A-G

http://identifiers.org/hco/12/GRCh38#92891833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95809725-A-C

92893396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95808901-C-T

92898897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95807342-T-A

92898932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95807310-G-A

92899418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95806738-C-T

92899755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95806335-C-T

92900381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95805454-A-G

92903688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95804644-A-G

http://identifiers.org/hco/12/GRCh38#92903699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95804635-A-C

92905680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95802801-G-T

92905885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95802570-C-T

92906810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95799979-T-C

92923935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95785291-T-C

92924997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95784194-C-T

92925120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95784069-T-C

92926410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95779302-G-A

92926502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95779198-C-T

92926965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95778742-A-G

92927255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95778431-A-T

92927409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95778278-T-C

92927410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95778277-T-C

92927475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95778216-T-C

92927639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95778067-G-A

92927738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95777973-T-C

92927960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95777749-A-G

92927972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95777737-T-A

92927972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95777737-T-C

92928591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95777183-T-C

92928820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95777031-G-A

http://identifiers.org/hco/12/GRCh38#92928921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95776950-C-A

92928921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95776950-C-T

92928927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95776946-G-A

92928927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 95776946-G-T

92928939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95776934-T-C

92928939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95776934-T-G

92928986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95776887-C-T

92928993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95776880-T-A

92928993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 95776880-T-C

92929112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 95776745-G-A

92929112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 95776745-G-C

92929234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 95776630-G-A

92929234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 95776630-G-T

http://identifiers.org/hco/12/GRCh38#92929321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#95776557-A-C

92929321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3185
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 95776557-A-G